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WORKING PARTIES ON LEUKAEMIA IN ADULTS AND CHILDREN
TRIAL IN ACUTE MYELOID LEUKAEMIA OR HIGH RISK
MYELODYS
PLASTIC SYNDROME 17
PROTOCOL FOR PATIENTS AGED 18 to 60
(Trial Reference ISRCTN55675535)
Through the use of a risk based approach AML17 will evaluate several relevant therapeutic
questions in acute myeloid leukaemia (AML) as defined by WHO, and high risk Myelodysplastic
Syndrome. The trial is open to all patients aged 18 to 60 years, and also to patients aged 60 years
or over for whom intensive therapy is considered appropriate. At least 2800 patients will be
recruited. For patients who do not have the Acute Promyelocytic Leukaemia (APL) subtype, an
induction randomisation will compare two courses of the standard ADE with ADE or DA each in
combination with one of two doses of the immunoconjugate Mylotarg in course 1 (five
options). Consolidation will compare one course with two courses (MACE/Midac versus
MACE).
After course 1 of treatment, patients will be segregated based on their molecular-genetic
characteristics, and a validated risk score. Patients who have a FLT3 mutation will be randomised
to receive, or not, the FLT3 inhibitor CEP-701 after each subsequent chemotherapy course.
Patients who are at high risk of relapse based on the AML Risk Score will be eligible for an
allogeneic stem cell transplant if a donor is available, and/or enter a study of a novel combination.
These
FLAG-Ida
Daunorubicin/Clofarabine with the aim of maximising the number of patients receiving an
allogeneic transplant.
Patients who have Core Binding Factor (CBF) ie favourable risk disease leukaemias will be
randomised only to the 3 versus 4 comparison. The rest of the patients will be randomised to
receive, or not, up to twelve treatments with the mTOR inhibitor, Everolimus in combination with
chemotherapy.
For patients with APL, the Italian AIDA anthracycline plus ATRA based chemotherapy approach
will be compared with the chemotherapy-free combination of ATRA plus Arsenic Trioxide.
At diagnosis, material will be sent to reference labs for molecular and immunophenotypic characterisation and the identification of markers of minimal residual disease (MRD) detection. The predictive value of these markers will be validated in the early part of the trial, and the clinical impact of this information will be tested in a randomised fashion in a later patient cohort. There are about 700 cases of AML aged 18-59 years per annum in the British Isles alone. About 650 patients entered AML15 annually, so with a continuation of accrual at this, or a higher level, clear evidence on the relative benefits of the therapeutic options being tested in AML17 will be obtained in just a few years. This information will contribute to the continuing improvement of the treatment available to many future patients with AML. This protocol is intended to describe a trial conducted by the AML Working Group of the National
Cancer Research Institute (NCRI) Haematological Oncology Study Group in Acute Myeloid
Leukaemia and high risk Myelodysplastic Syndrome under the sponsorship of Cardiff University. It
provides information about procedures for the entry, treatment and follow-up of patients. It is not
intended that this protocol should be used as an aide-memoire or guide for the treatment of other
patients. Every care has been taken in its drafting, but corrections or amendments may be
necessary. Before entering patients into the trial, clinicians must ensure that the trial protocol has
received clearance from their Local Research Ethics Committee and the participating Institution's
Research and Development Office. During the course of this 6-year trial, not all randomisation
options will be open at all times and some additional options may be included by protocol
amendment.
Clinicians are required to read the whole protocol before commencing treatment

Version 2: May 2008 Version 2: May 2008 TRIAL MANAGEMENT GROUP
CHIEF INVESTIGATORS
Professor A K Burnett
Professor N H Russell
Department of Haematology Haematology Department School of Medicine Cardiff University Nottingham NG5 1PB Cardiff CF14 4XN Tel: 01159 627708 Tel: 02920 742375 Fax: 01159 627742 Fax: 02920 744655 Email: [email protected] Email: [email protected]
STATISTICS/DATA MANAGEMENT
STATISTICS
Dr Robert Hills
Professor K Wheatley
Department of Haematology Clincial Trials Unit School of Medicine CRUK Institute of Cancer Studies Cardiff University University of Birmingham Cardiff CF14 4XN Birmingham B15 2TT Tel: 02920 744647 Tel: 0121 4143366 Fax: 02920 744655 Fax: 0121 4143700 Email: [email protected] e-mail: [email protected] CLINICAL COORDINATORS
Dr D Milligan
Dr A Hunter
Department of Haematology Department of Haematology Birmingham Heartlands Leicester Royal Infirmary Infirmary Square Bordesley Green East Leicester LE1 5WH Birmingham B9 5ST Tel: 0116 258 6602 Tel: 0121 424 3699 / 2699 Fax: 0116 258 5093 Fax: 0121 766 7530 Email: [email protected] Email: [email protected] Dr Mike Dennis
Professor Richard Clark
Haematology and Transplant Unit The University Department of Haematology Christie Hospital NHS Trust Royal Liverpool Hospital Tel: 0161 446 8420 Liverpool L69 3BX Fax: 0161 446 3940 Email: [email protected] Email: [email protected] Dr David Bowen
Dr Jenny I O Craig
Department of Haematology Consultant Haematologist Leeds General Infirmary Addenbrooke's Hospital Gt. George Street Tel: 01223 596289 Email: [email protected] Fax: 01223 216407 Email: [email protected] Dr Panos Kottaridis
Dr Paresh Vyas
Consultant Haematologist Honorary Consultant Haematologist Royal Free Hospital Department of Haematology Version 2: May 2008 Weatherall Institute of Molecular Medicine University of Oxford John Radcliffe Hospital Tel: 0207 830 2301 Ext: 3257 Fax: 0207 830 2092 Tel: 01865 310825 Email: [email protected] Email: [email protected] Professor M F McMullin
Consultant Haematologist Cancer Research Centre Queen's University Belfast City Hospital Lisburn Road BELFAST BT9 7AB Tel: 028 90 329241 Ext: 2242 Email: [email protected]
PHARMACOVIGILANCE
Dr Jonathan Kell (Clinical)
Mrs Alison Jenkins (Pharmacovigilance Officer)
Consultant Haematologist Cancer Trials Unit University Hospital of Wales University Hospital of Wales Cardiff CF14 4XN Cardiff CF14 4XN Tel: 02920748276 Tel: 02920746413 Fax: 02920 743439 Fax: 02920 742289 Professor C Craddock
Department of Haematology Queen Elizabeth Medical Centre Edgbaston Birmingham B15 2TH Tel: 0121 472 1311 Ext: 8145 Fax: Email: [email protected]
MOLECULAR DIAGNOSIS AND MONITORING
Professor David
Professor J A L Yin
Professor Rosemary Gale
Grimwade*
Department of Haematology Cancer Institute, Department of Department of Medical and Manchester Royal Infirmary Molecular Genetics Paul O'Gorman Building 8th Floor, Tower Wing University College London 72 Huntley Street [email protected] E-mail: [email protected] Professor Ken Mills
Dr Sylvie Freeman
Professor of Experimental Clinical Immunology Division of Infection and Queens University Belfast University of Birmingham Version 2: May 2008 Belfast, BT9 7AB E-mail: [email protected] Tel: 02890972786 Direct Birmingham, B15 2SZ Tel: 01214158759 Mob: 07884310528 Fax: 01214143069 [email protected] *All APL samples to be sent directly to: Molecular Oncology Diagnostics Unit, Clinical Laboratory Services,
4th Floor Southwark Wing, Guys Hospital, Great Maze Pond, London SE1 9RT

FLT3 INHIBITION
mTOR INHIBITION
TISSUE ARCHIVE
Dr S Knapper
Dr Emma Das Gupta
Professor David Linch
Department of Haematology Department of Haematology Cancer Institute, Department of School of Medicine Nottingham City Hospital Cardiff University 2nd Floor/Clinical Sciences Paul O'Gorman Building University College London Cardiff CF14 4XN 72 Huntley Street Tel: 02920745379 Fax: 02920744655 Nottingham NG5 1PB Tel: 0115 9627708 [email protected] Fax: 0115 9627742 Email:[email protected] [email protected] LABORATORY STUDIES
CYTOGENETICS
WALES CANCER TRIALS UNIT
Prof C Harrison
Mr Gareth Griffiths
Leukaemia Research Cytogenetics Group, Scientific Director
Northern Institute for Cancer Research, Wales Clinical Trials Unit Newcastle University, Neuadd Meirionnydd Level 5, Sir James Spence Institute, University Hospital of Wales Royal Victoria Infirmary, Queen Victoria Road, Newcastle upon Tyne Tel: 02920 687457 WELSH CANCER TRIALS UNIT 12 CATHEDRAL ROAD AND FOLLOW-UP (WCTU): CARDIFF CF11 9LJ 02920 196800
Fax: 02920 196818
Telephone randomisation availability:
09.00-17.00 hours, Monday to Friday (except bank holidays)
24 hour internet randomisation and data entry:
Version 2: May 2008 CONTENTS
ETHICAL CONSIDERATIONS . ERROR! BOOKMARK NOT DEFINED.
OBJECTIVES . 2
TRIAL DESIGN . 3
JUSTIFICATION OF TRIAL DESIGN AND TREATMENT SCHEDULES . 7
RANDOMISATION AVAILABILITY . 17
REFERENCES . 18
INCLUSION AND EXCLUSION CRITERIA . 23
PROCEDURES FOR ENTRY INTO THE TRIAL AND DATA RECORDING . 24
INDUCTION CHEMOTHERAPY: COURSES 1 AND 2 . 29
10 ASSESSMENT OF RESPONSE . 30
11 ADDITIONAL TREATMENTS . 32
11.4 CORE BINDING FACTOR LEUKAEMIA . 35
11.5 HIGH RISK SCORE PATIENTS. 36
12 CONSOLIDATION RANDOMISATION . 38
13 CONSOLIDATION CHEMOTHERAPY: COURSES 3 AND 4 . 39
14 STEM CELL TRANSPLANTATION . 40
15. ARRANGEMENTS FOR MOLECULAR SCREENING AND MINIMAL RESIDUAL
DISEASE MONITORING . 41
16. MANAGEMENT OF PATIENTS WHO RELAPSE OR ARE REFRACTORY . 48
17. SUPPORTIVE CARE . 48
18. CNS TREATMENT FOR ADULTS . 49
19 ACUTE PROMYELOCYTC LEUKAEMIA………………………………………………….49
20. STATISTICAL CONSIDERATIONS . 57
21. TRIAL GOVERNANCE AND ADVERSE EVENT REPORTING . 59
APPENDICES:
A WHO histological classification of Acute Myeloid Leukaemias . 62
B Preparation, administration and toxicity of drugs used in AML15 . 63
C Background information on CEP-701 . 74
D Instructions to the patient/caregiver for administering CEP-701 . 81
E Procedure for bone marrow transplantation . 83
F Derivation of a risk score for younger adults . 86
G Supportive care recommendations for acute promyelocytic leukaemia . 90

Version 2: May 2008 ETHICAL CONSIDERATIONS
The AML17 Trial Protocol has been approved by the Wales Multicentre Research Ethics Committee (NRES) and must also be approved by the Local Research Ethics Committee (LREC) at each centre before patients are entered. A copy of a centre's LREC approval must be lodged with the Trial Office before entry of patients can commence at that centre. Centres are required to go through a registration process with the Trial Office before recruitment is started. The institution's Research and Development Office must complete the site agreement with Cardiff University. The right of a patient to refuse to participate in the trial without giving reasons must be respected. After the patient has entered the trial, the clinician is free to give alternative treatment to that specified in the protocol at any stage if he/she feels it to be in the patient's best interest, and the reason for doing so should be recorded. Similarly, the patient must remain free to withdraw at any time from protocol treatment without giving reasons and without prejudicing any further treatment. All patients who come off protocol therapy for whatever reason will still need to remain within the study for the purposes of follow-up and data analysis. The AML17 trial will be conducted in accordance with the Medical Research Council's Guidelines for Good Clinical Practice in Clinical Trials (a copy of these may be obtained from the MRC or from the Trial Office). Version 2: May 2008 Section A: TRIAL SUMMARY
OBJECTIVES
The AML17 trial has two distinct parts: i. For patients with acute myeloid leukaemia (AML), (other than acute promyelocytic leukaemia) and High Risk Myelodysplasia, as defined by the WHO Classification (2001) (Appendix A). For adults with acute promyelocytic leukaemia (APL).
The objectives for each of these components are summarised below.
2.1 Therapeutic questions for patients with non-APL AML and High Risk
Myelodysplastic Syndrome
For patients with acute myeloid leukaemia (AML) the aims of the AML17 trial are:
 To compare five induction chemotherapy schedules (namely ADE versus ADE +
Mylotarg (3mg/m2 ) or ADE + Mylotarg (6mg/m2) or DA + Mylotarg (3mg/m2 ) or
DA + Mylotarg (6mg/m2) , given in course 1).

 To compare a total of three versus four courses of treatment in total, comparing
MACE versus MACE/MidAc in consolidation.
— To assess the value of the FLT3 inhibitor CEP-701 for patients with a FLT3 mutation
— To assess the value of mTOR inhibition in patients who lack a FLT3 mutation, and
who are not high risk, and who do not have Core Binding Factor Leukaemia In high risk patients to compare novel treatment, Daunorubicin/Clofarabine vs
standard FLAG-Ida.
—
In high risk patients, to evaluate, the value of allogeneic stem cell
transplantation (SCT), whether standard allogeneic (allo-SCT) or non-
myeloablative "mini" allogeneic (mini-SCT).
To assess the clinical value of minimal residual disease (MRD) monitoring for
patients' overall survival.
2.2 Therapeutic questions for patients with APL
For patients with APL the aims of the AML17 trial are:  To compare the Idarubicin based, AIDA Schedule with the chemo-free
combination of ATRA and Arsenic Trioxide.
 A full description of the trial intentions for patients with APL are set out in Section Version 2: May 2008 2.3 Endpoints for Patients who have non-APL AML
The main endpoints for each comparison will be: Complete remission (CR) achievement and reasons for failure (for induction questions). Duration of remission, relapse rates and deaths in first CR. Overall survival.  Toxicity, both haematological and non-haematological  Quality of life for patients in the disease monitoring randomisation — Supportive care requirements (and other aspects of health economics). 2.4 Subsidiary objectives
Blood and bone marrow will be required at diagnosis, during remission and at relapse to evaluate the therapeutic relevance of morphological, cytogenetic, molecular-genetic and immunophenotypic assessments, with particular respect to: The relevance of the molecular and immunophenotypic detection of minimal residual disease The relevance of the presence of a cytogenetic abnormality in the bone marrow of patients in morphological remission. To correlate the blood level of anti-FLT3 activity and the extent of dephosphorylation of the FLT3 receptor with response for patients allocated to receive FLT3 inhibition therapy To assess the level of plasma mTOR activity in relation to clinical outcome. To store excess diagnostic material for future research. TRIAL DESIGN

AML17 is a randomised, controlled, open label Phase III trial for patients with AML and High
Risk Myelodysplastic Syndrome (MDS). The design may, at first sight, appear complicated.
However, if the trial is broken down into separate sections, each phase is straightforward and
should be readily understandable to both clinicians and patients and of similar complexity to
other NCRI AML trials:
3.1 Summary of comparisons

AML (other than APL):
A. Induction phase: one randomisation to one of five arms. B Consolidation phase: for patients who are not high risk two versus one further treatment courses (two arms) C FLT 3 inhibition for patients with FLT 3 mutations: one randomisation (two arms). Version 2: May 2008 D For high risk patients standard therapy (FLAG-Ida) vs D/Clofarabine E mTOR inhibition (two arms) A. AIDA versus ATRA plus Arsenic Trioxide (two arms) AML (other than APL)
There are six randomised comparisons within the trial: (i) ADE versus ADE with Mylotarg 3mg/m2 or 6mg/m2 versus DA with Mylotarg 3mg/m2 or 6mg/m2 (five comparisons) End of Course 1 (ii) FLT3 inhibitor (CEP-701) versus not, for FLT3 mutation positive (iii) FLAG-Ida versus D/Clofarabine for high risk score cases. (iv) mTOR inhibition for non-CBF Leukaemias After Course2 (v) 1 versus 2 additional courses (i.e. 3 versus 4 courses of therapy in total) for patients who are not poor risk who have entered complete remission. Chemotherapy will be MACE versus MACE/Midac. (vi) Patients will be invited to enter a randomisation between minimal residual disease monitoring or no monitoring. In poor risk patients, the role of allogeneic SCT of either Standard or Reduced intensity will be assessed by means of a genetic randomisation (i.e. donor versus no donor comparison). Full details of the rationale for these comparisons, progress through the trial and treatment can be found in the relevant sections of the protocol, but are summarised below (and in the flow diagrams at the front and back of the protocol): 1. At diagnosis: randomise between ADE and ADE or DA each with one of two doses of Mylotarg as induction chemotherapy.
The Five induction treatment arms will therefore be:
Arm A Two Courses of ADE
Arm B Two courses of ADE with Mylotarg 3mg/m2 on day 1 of course 1
Arm C Two courses of ADE with Mylotarg 6mg/m2 on day 1 of course 1
Arm D Two courses of DA with Mylotarg 3mg/m2 on day 1 of course 1
Arm E Two courses of DA with Mylotarg 6mg/m2 on day 1 of course 1
Version 2: May 2008 2. By the end of the first course of induction chemotherapy, the FLT3 mutation, cytogenetics and molecular screening (Core Binding Factor), and Risk Index status of each non-APL patient will be available. i) Patients with a FLT3 mutation can then be randomised to start FLT3 inhibition or not for four courses after each course of chemotherapy (Sections 4.1.3 and 11.3) ii) Patients who have a high risk score will enter the comparison of Daunorubicin/Clofarabine versus FLAG-Ida (Section 11.5) iii) Core Binding Factor Leukaemias will be randomised to three or four courses of iv) Other patients who are not involved in the options (i) to (iii), will be randomised to receive the mTOR inhibitor for 12 infusions of treatment (Section 11.6) v) All patients except the High Risk Index patients will receive the second induction treatment course. 3. Following the first and second course of treatment, patients should have a bone marrow (and paired blood sample) for MRD assessment (see Section 15). 4. On recovery from course two, patients will be randomised to one versus two further treatment courses in total. The consolidation will be MACE or MACE + Midac: Arm F: MACE
Arm G: MACE
5. Patients who are not in CR following the second course of treatment ie have refractory disease,are also eligible to enter the high risk randomisation. NB Consolidation for children will comprise 2 courses of either MACE+MidAc or
High Dose Ara-C (See Section 13)
3.3 Acute Promyelocytic Leukaemia (APL)
There is one randomisation within the trial: (i) AIDA versus ATRA plus Arsenic Trioxide.
Full details of the rationale for these comparisons, progress through the trial and treatment can be found in the relevant sections of the protocol, but are summarised below (and in the flow diagrams on the front and back covers): 1. At diagnosis: Patients will be randomised between the AIDA (4 courses of Ida based chemotherapy) and the chemotherapy free approach of four courses of ATRA combined with Arsenic Trioxide. Version 2: May 2008 2. Patients who present with a white cell count of >10x109/l should receive mylotarg (6mg/m2) to reduce the WBC in addition to the allocated treatment 3. After 55 to 60 days assess remission status (see Section 19). 4. After Course 2, reassess remission status for minimal residual disease monitoring: - If in morphological CR, continue with AML17 protocol. - If not in morphological or molecular CR, the patient should be treated with Arsenic Trioxide or Mylotarg. - Bone marrow should be sent for MRD monitoring. 5. After courses three and four and at subsequent specified intervals, bone marrow should be sent for molecular monitoring (see section 15) Version 2: May 2008 Section B: RATIONALE FOR
TREATMENT INTERVENTIONS
JUSTIFICATION OF TRIAL DESIGN AND TREATMENT SCHEDULES

4.1 AML (excluding APL)

4.1.1 Experience from AML15
It is clear that AML15 was a highly successful trial with recruitment at an unprecedented level (60 patients per month), a high overall CR rate of 84%, and survival which is significantly improved compared with the previous MRC AML12 trial and which compares very favourably with any international protocol. Thus, the therapy used in AML15 forms the backbone of the AML17 trial. The theme for AML 17 is best available chemotherapy with or without molecular intervention, and, for patients who are at high risk of relapse, novel treatment will be assessed in a "pick a winner" design. The choice of induction treatments was informed by the preliminary experience from AML15. Although longer follow up is required there is ample evidence that the FLAG-Ida schedule was significantly more myelosuppressive and required more supportive care with the associated economic implications. Preliminary analysis does not suggest that any potential benefit would out weigh this. It is possible that later benefits may emerge. The addition of Mylotarg to induction course 1, initially at least, has significantly reduced the risk of relapse and improved the disease free survival, but this has not yet translated into a significant overall survival advantage(1). Of note was that there was very little increase in overall toxicity with the Mylotarg set at the low dose of 3mg/m2. Other studies have used a dose of 6mg/m2 in combination so there is a basis to examine a higher Mylotarg dose(2). While the results of AML15 suggest that DA + Mylotarg is superior to DA alone, because recruitment to the ADE +/- Mylotarg opened later it is not clear whether ADE + Mylotarg is superior to ADE alone or indeed whether DA + Mylotarg is better than ADE alone. It is therefore important to establish whether the addition of Mylotarg to ADE is beneficial, and whether the addition of Mylotarg as a third drug to DA is better than Etoposide as the third drug. In consolidation, in spite of the fact that around 1000 patients were randomised between MRC consolidation (MACE/MidAc) and high dose Ara-C (HD-AraC), it is not possible at this point to be sure whether or not a difference exists between these schedules. Longer follow up will be required of the randomised patients to establish if one or other approach is superior. AML17 will therefore continue to be based on the MRC consolidation chemotherapy of MACE and MidAc. This may however be subject to change if it emerges that high dose Ara-C is superior consolidation. There is uncertainty as to how many total courses of chemotherapy are optimal. This clearly has significant importance for the patient's experience and the associated resource use. Both the AML12 and AML15 trials compared four versus five courses and have not found a significant benefit of adding a fifth treatment course. For various reasons, in both trials some patients only received 3 treatment Version 2: May 2008 courses. We have conducted a careful retrospective comparison of these patient groups, excluding only patients who could not have received the fourth course of treatment, and, using an analysis adjusted for risk factors, we have evidence that the survival in both good and standard risk patients was comparable whether 3 or 4 courses were given. This is an imperfect comparison, but it justifies a prospective evaluation of this question. Therefore the AML 17 trial will randomise patients after course 2 to one or two more courses of treatment (i.e. a total of three versus four courses). 4.1.2 Interventions Based on Molecular Genetic Characteristics and Risk Score

The genetic and molecular heterogeneity of AML is well known(3). To date
consolidation treatment in our group's trials have been guided by the cytogenetic
information, such that patients with adverse cytogenetics, or with inadequate
responses to induction chemotherapy, were segregated off to receive an
allogeneic stem cell transplant or alternative chemotherapy, while good risk
patients were advised not to undergo transplantation.
Recently, we have had concerns that the cytogenetic prognostic score is not
sufficiently sensitive to the risk profile of individual patients who have entered
complete remission (CR). In part this was based on the lack of a demonstrable
survival advantage in any of the three risk groups for transplantation. To that end
we have devised a new risk score based on modelling outcomes of patients
entering AML10 and AML12 (described in appendix F), which divides patients into
three groups with 5-year survivals of 63%, 47% and 24%, and which was
prospectively validated using data from AML15(4). The important effect when
compared with the cytogenetic risk definition is to move approximately one sixth of
the patients who were previously standard risk into the high risk category and to
move about one tenth of previously poor risk patients into the standard risk group.
The net effect is that 27% of patients in AML10, & 12 are now defined as high risk
compared with 17% previously. When we examine the role of transplantation on
the new high risk group, Mantel-Byar analysis shows a significant survival
advantage, although in the light of possible selection biases this result needs to be
interpreted cautiously. It is clear from the nearly 8000 patients entered into the
MRC AML10, 12 and 15 trials that there has been no improvement in survival for
high risk patients, however defined, for the last 20 years. The AML17 trial,
therefore, compares a novel combination (Daunorubicin/ Clofarabine) with FLAG-
Ida with a view to proceeding to allogeneic transplantation.
4.1.3 FLT3 Inhibition

A number of prognostic factors have been identified for CR and relapse. Among the adverse prognostic factors is the fms-like tyrosine kinase 3 (FLT3) activating mutation. These mutations spontaneously initiate ligand-independent autophosphorylation of the receptor, stimulating proliferation of AML cells. Two types of FLT3 activating mutations have been identified in patients: an internal tandem duplication (ITD) and a point mutation, usually at aspartate 835. The presence of FLT3/ITD mutations has been shown to be associated with a decreased remission induction rate and poorer outcome in paediatric AML and a higher rate of relapse and poorer overall survival in adult AML(5-10). Version 2: May 2008 Studies in animals suggest that inhibition of mutated FLT3 improves response to chemotherapy and/or overall survival(11,12). CEP-701 is a potent FLT3 inhibitor and induces a cytotoxic-like effect on both FLT3/ITD transfected cells and primary leukaemic myeloblasts in patients with AML with the FLT3/ITD mutation. In a mouse model of FLT3/ITD leukaemia, treatment with CEP-701 significantly prolonged survival. In a recently completed Phase II clinical trial in patients with relapsed disease, CEP-701 at doses of 60 and 80 mg bd was associated with transient decreases in the number of peripheral AML myeloblasts(12). A similar response was seen in a UK Phase II study in untreated older patients(13). A pharmacokinetic /pharmacodynamic analysis indicated that this anti-leukaemic activity required a high degree of inhibition of the target kinase, FLT3(14). In vitro studies have shown that AML cells that survive chemotherapy treatments remain responsive to CEP-701 (Levis, personal communication, 2003). There is in vitro data to suggest that combining CEP-701 with Ara-C has a synergistic effect(15). This has led to an ongoing randomised study in relapsed AML which compares high dose Ara-C with and without sequential CEP-701. In a preliminary analysis performed after the first 49 patients, 11 of 24 patients who had the combination arm achieved a CR or CRi compared with 6 of 25 in the chemotherapy only arm (P Brown, personal communication). Similar preliminary data is also emerging from the combination of another FLT3 inhibitor (PKC412) in relapsed disease(16). An objective of the AML17 trial is to determine whether CEP-701, given in sequence with standard chemotherapy in first line, can reduce the risk of relapse and improve survival in patients who have a FLT3 mutation. Background information on the non-clinical pharmacology and pharmacokinetics, toxicology, and clinical experience both in healthy subjects and patients with cancer is given in Appendix C. Of potential clinical relevance is the theoretical interaction with azole antifungal agents which use CYP3A4 in metabolism, with the potential effect of increasing blood levels of CEP-701. The extent to which this happens and whether it is clinically relevant is not known. As part of the assessment of CEP-701 in this trial, blood levels of free CEP-701and azole blood levels will be measured on day 14 of each course of CEP-701 treatment. 4.1.4 Core Binding Factor Leukaemias
This subgroup is characterised by having either the t(8;21) or inv(16)/t(16;16) balanced chromosomal rearrangements which result in the production of a fusion transcript namely the AML1-ETO and CBFβ-MYHII respectively. These provide potentially useful molecular targets for monitoring minimal residual disease (MRD). Patients with these lesions have tended to be more sensitive to intensive treatment with a 5-year survival of around 65%. Nevertheless, there is still a significant chance of relapse. Approximately 30 to 35% of cases have a c-KIT mutation which is associated with a significantly increased risk of relapse(17), and, therefore, the addition of a tyrosine kinase inhibitor with anti-KIT activity, such as Dasatinib or PKC412, would be a potential new treatment option for the AML17 trial. However the data from AML15 concerning Mylotarg in this subgroup suggests that they appear to benefit particularly from the administration of Mylotarg in course 1. The recent analysis of AML15 indicates that the survival of Core Binding Factor Leukaemia patients who have received Mylotarg in course 1 Version 2: May 2008 is 87% at 4 years. This means that a comparative study of Dasatinib/PKC 412 is not statistically viable in AML17 since most patients in AML 17 will receive Mylotarg in course 1. The new inhibitors are intended to be available to trial entrants if they relapse or are designated to be at high risk due to persistence of minimal residual disease. In the design of AML17 CBF Leukaemia patients have a 1 in 5 chance of receiving ADE only, ie avoiding Mylotarg, which is not considered to be in their interests, so they will be eligible to be randomised to receive one of the two Mylotarg doses on day one of course 2, and will contribute to the three versus four question in consolidation. 4.1.5 Other Patients
Approximately 60% of all non-APL patients have neither a FLT3 mutation nor Core
Binding Factor Leukaemia. Approximately half of these patients will have high risk
disease as defined by our new risk score. These patients merit evaluation of novel
treatment approaches and/or should be offered stem cell transplantation.
4.1.5.1
High Risk Score
To date post induction treatment decisions have been substantially based on cytogenetics. Because of concerns that this definition was not sensitive enough at an individual patient level a retrospective analysis was undertaken on patients in the AML10 & 12 trials using a Cox proportional hazards model to provide a number of weighted factors which would be available after treatment course 1 which could provide a risk index for survival from CR. The central concern was whether there were subgroups of patients who were missing out on an effective treatment eg stem cell transplantation. The parameters in the index and the derivation of the score are shown in Appendix F. The cut points for designating patients as good, standard or high risk are to an extent arbitrary, and the index could be refined as new prognostic markers are incorporated eg FLT3 status. FLT3 has been excluded from the score to be used in AML17 because such patients are being assessed in the FLT3 inhibitor part of AML17. For the purposes of the AML17 trial patients who have a risk score of greater than 2.667, who do not have a FLT3 mutation or Core Binding Factor Leukaemia will be designated as high risk with a predicted survival at 5 years of 24% (based on AML10, 12). This will comprise approximately 30% of all patients who enter CR. Retrospective information indicates that this group of patients may have an improved survival following transplant (33% vs 20%), so at the present level of knowledge a stem cell transplant from a sibling or unrelated matched donor may well be indicated. However new treatments need to be found for these patients to improve outcome per se, or to increase the number who can get to transplant.The new generation nucleoside analogue, Clofarabine has proved to be an effective agent as monotherapy, particularly in patients with high risk cytogenetics. As a prelude to the NCRI AML16 trial, we developed the combination of Daunorubicin and Clofarabine. In the pilot study this proved to be both effective and tolerated without additional toxicity. More than 100 patients in AML16 have now received this combination without difficulty. This combination will therefore be compared to the FLAG-Ida schedule which in the AML15 trial appeared to give a trend to superiority over the DA or ADE combination. The aim of this comparison is to Version 2: May 2008 increase the number of patients reaching transplant and to reduce the risk of
relapse. It is expected that a donor (sibling or unrelated) will be found for most
patients.
4.1.5.2
m TOR Inhibition
Constitutive activation of the PI3K/AKT pathway has been demonstrated in 90% of AML samples where it has been shown to be central to the survival of AML blasts but not of normal CD34+ cells(18,19). The pathway is of particular relevance to AML as it is also activated by FLT3. The serine/threonine kinase mTOR is downstream of PI3K/AKT and can be inhibited by mTOR inhibitors including Sirolimus and its analogue Everolimus (RAD001, Novartis). Studies in NOD/SCID mice have indicated that mTOR may regulate a critical cell survival pathway in AML stem cells(19) and Sirolimus may have the potential to eliminate leukaemia-initiating stem cells without eliminating normal haematopoietic stem cells. Sirolimus strongly inhibits the growth of AML cell lines in vitro and dephosphorylation of downstream effectors of mTOR in a Sirolimus-sensitive manner has been demonstrated in 23 AML cases(20). It has also been shown that increased survival, proliferation and leukaemic transformation of cell lines by FLT3/ITD is mediated by AKT and mTOR and can be inhibited by Sirolimus at therapeutically achievable concentrations(21). In an unrandomised clinical trial, Sirolimus was administered as a single agent to 9 relapsed, refractory or poor-risk AML patients for 28 days at doses used for renal transplant recipients. At day 28, partial responses had occurred in 4 patients whilst one had stable disease and 4 had progressed(22). In an ongoing trial at Nottingham University Hospitals,11 elderly patients with primary and relapsed AML have been treated with the combination of low dose Ara-C and Sirolimus. Following a single 28-day course of treatment, of the 7 patients eligible for analysis, one had achieved a CR, 4 a PR, one marrow was profoundly hypocellular and one patient was a non-responder. Patients in this trial reliably maintained trough Sirolimus levels of 8-16 ng/ml, which are consistent with the published concentrations required to inhibit AML cell growth in vitro(23). The feasibility of combining mTOR inhibition (Sirolimus) with intensive chemotherapy has also been assessed in AML patients in conjunction with the more intensive MEC (Mitoxantrone, Etoposide and Cytarabine) chemotherapy regimen in a phase I dose escalation study in which standard renal transplant doses were well tolerated and did not increase the non-haematologic toxicity of MEC chemotherapy with a median time to ANC recovery of 27 days(24). This provides a rationale for examining the addition of an mTOR inhibitor to allocated chemotherapy in the AML17 trial. Temsirolimus (CCI-779, Wyeth Research) has been evaluated in a number of solid tumours and has been recently approved by the FDA for the indication of advanced renal carcinoma. It is most reliably dosed by a single intravenous infusion weekly. RAD001 (Everolimus-Novartis) has shown pre-activity against numerous cell lines and in vivo models. It has also had extensive pre-clinical assessment in combination with several chemotherapeutic agents. In human studies on several hundred patients a steady state AUC can be achieved by daily or weekly oral administration with a half life of approximately 30 hours. A number of studies of RAD001 in combination with chemotherapy have been carried out. As Version 2: May 2008 (CerticanR) it is approved for prophylaxis of organ rejection in adults receiving allogeneic renal or cardiac transplants. RAD001 (Everolimus) has been in clinical development since 1996 as an immunosuppressant, associated with cyclosporin and glucorticoids, for the prevention of rejection in patients undergoing solid organ transplantation. In this context mTOR inhibition opposes interleukin-stimulated proliferation of activated T-lymphocytes. An antiproliferative effect on immuno-competent cells is also the rationale for investigation of the drug's activity in autoimmune diseases. The drug is also being investigated for use in the inhibition of initial proliferation after coronary angioplasty through its incorporation into drug-eluting stents. Pre-clinical investigations have demonstrated that RAD001 is a potent inhibitor of the proliferation of a range of human tumour cell lines in-vitro and inhibits tumour growth in-vivo in both xenografted, syngeneic and orthotopic animal models. Studies have also demonstrated the drug's inhibition of endothelial proliferation and its antiangiogenic activity. Experiments show the potential for combining RAD001 with other anticancer agents including paclitaxel, doxorubicin, cisplatinum, carboplatinum, gemcitabine, radiotherapy, imatinib, EGFR and VEGF inhibitors, and letrozole. Clinical trials of RAD0001 in oncology patients are ongoing since 2002 and include Phase I dose escalating studies as single agent, Phase II/III studies of RAD001 in indications where mTOR is known to be active, Phase I/II studies in combination with other anti-cancer agents and correlative investigations in the search for potential biomarkers. 4.2 Stem Cell Transplantation
There was a modest overall survival advantage of allogeneic SCT in the MRC AML10 Trial, but there was sufficient uncertainty to justify continuing to address the question in standard and high risk patients in the MRC AML12 trial. In the AML12 trial where risk was defined only on cytogenetics and morphological response to course 1, there was no overall survival benefit for transplant in either risk group. Nevertheless the AML15 trial permitted standard risk patients who had a matched sibling donor to go forward to transplantation including a reduced intensity allograft, and for high risk patients a matched unrelated donor was permitted. The comparative results of transplantation in the AML15 trial is not yet available, but both the reduced intensity allograft and transplant from an unrelated donor deliver a similar survival to a matched sibling transplant. In this large dataset the new risk score was used, in a retrospective analysis, to re-examine the role of transplantation. In patients with an intermediate score there was again no survival benefit from transplantation, however in the newly defined high risk score patients there was a significant survival difference (33% vs 18%, p=0.01). This leads to the conclusion that the risk score can identify a population of patients which benefits from transplantation, and comprises a larger population than defined as high risk by previous criteria. However only 30% of such patients received a transplant Version 2: May 2008 and relapse after transplant is still an important reason for patients failing. The aim of the AML17 trial in this group is to develop novel treatments which are better able to get a patient to transplant, by reducing early relapse, and similarily to reduce the risk of post transplant relapse. The value of transplantation will continue to be assessed by a comparison of patients who were and were not transplanted using the methods described in the statistical plan. 4.3 Acute Promyelocytic Leukaemia (APL)
Acute promyelocytic leukaemia (APL) is a particular subtype of acute myelogenous leukaemia (AML) characterised by consistent clinical, morphologic, and genetic features. These features include the frequent association at diagnosis of a severe hemorrhagic diathesis, a striking sensitivity to anthracyclines, and the response in vitro and in vivo to differentiation therapy with retinoid derivatives such as all-trans retinoic acid (ATRA)( 26-28 ). At the molecular level, APL blasts are characterised by a specific chromosomal translocation t(15;17) resulting in a hybrid PML/RAR gene which is readily identified by reverse-transcriptase polymerase chain reaction (RT-PCR)(29-32 ). In addition to its diagnostic relevance, detection of the PML/RAR hybrid by sensitive RT-PCR techniques is relevant to assess response to therapy and for the monitoring of minimal residual disease (MRD) during follow-up. In fact, several prospective studies using RT-PCR methods with sensitivity between 10-3 and 10-4 have shown that the achievement of PCR-negative status is associated with prolonged survival and higher probability of cure, whereas persistence of, or conversion to PCR-positivity in bone marrow after consolidation is invariably associated with subsequent haematologic relapse (reviewed in(33,34)). As a consequence, the achievement of molecular remission is nowadays universally considered as a therapeutic objective in this disease(35). Furthermore, preliminary evidence from the pre-arsenic era has suggested that early therapy of APL recurrence at time of molecular relapse is advantageous over delaying treatment until haematologic relapse(36,37). The development of real-time quantitative PCR (RQ-PCR) methods has recently provided an opportunity to better assess at the quantitative level the kinetics of PML/RARα reduction and that of disease relapse in the individual patient. In addition, RQ-PCR permits the identification of poor quality samples Version 2: May 2008 which give rise to "false negative" results and facilitates the standardised analysis of samples in the context of multi-centre clinical trials( 33,34). As reported in several large multicentre trials, front-line use of combined ATRA and anthracycline chemotherapy results in long-term remission and potential cure in >80% of newly diagnosed APL patients( 38-50). The Italian multicentre Group GIMEMA reported in 1997 high rates of molecular remission in newly diagnosed and genetically confirmed APL using a simultaneous ATRA plus Idarubicin (AIDA) combination for induction treatment, followed by 3 courses of intensive chemotherapy as consolidation(38). This protocol, with slight modifications, was subsequently adopted by other groups including the Spanish PETHEMA cooperative group who reported similar antileukaemic efficacy despite omitting Ara-C and other non-intercalating agents from the original AIDA, with the advantage of sparing toxicity and increasing compliance to treatment(50). Based on a meta-analysis of the two studies, a stratification score was developed which distinguished patients into high, intermediate and low relapse risk categories according to initial WBC and platelet counts. According to this system, patients with WBC >10x109/L had significantly higher relapse risk(49) . Two independent risk-adapted studies were therefore designed by the PETHEMA and GIMEMA in which treatment intensification was planned according to the relapse risk. The results of both studies showed improved outcomes by adding ATRA for consolidation to the original AIDA scheme(50,51). In particular, the GIMEMA reported significantly improved antileukaemic efficacy and reduction of the relapse rate in the high risk group by administering ATRA in addition to Ara-C(51) In line with these findings, most studies nowadays include risk-adapted approaches in which treatment intensification is based on initial WBC counts(47). Despite the dramatic progress achieved in front-line therapy of APL with the ATRA/chemotherapy combination, treatment failure still occurs in approximately 15% of patients. Moreover, these regimens are associated with significant toxicity due to severe myelosuppression frequently resulting in life-threatening infections, and with serious, though infrequent complications such as cardiomyopathy and the occurrence of secondary myelodysplastic syndromes and/or acute myeloid leukaemias(52,53). Several means are available to decrease toxicity in the treatment of newly diagnosed APL, including the availability of less toxic and highly effective agents such as arsenic trioxide (ATO) and the possibility of stringent MRD monitoring offered by RT-PCR. Following the demonstration of its striking activity in relapsed patients(54-63) arsenic trioxide (ATO) has been licensed in the USA and Europe for the treatment of relapsed and refractory APL. Arsenic derivatives had been used since ancient times in Chinese medicine for the treatment of malignant and inflammatory diseases. The mechanism of action of ATO in APL is complex and not yet known in detail. At a high concentration (0.5 to 2.0 µmol/L) ATO induces apoptosis in vitro, through induction of caspases 2 and 3, while at lower concentrations (0.1 to 0.5 µmol/L) it induces partial differentiation of leukaemic promyelocytes through PML/RARα degradation; furthermore, ATO is known to inhibit angiogenesis via down-regulation of vascular endothelial growth factor (VEGF)(63-66). Concerning its toxicity profile, ATO is usually well tolerated and its use is associated with a series of manageable adverse events including hyperleucocytosis, the APL differentiation syndrome, prolongation of the QT interval, peripheral neuropathy, mild myelosuppression, hyperglycaemia and hypokalaemia(67). Of these, QT prolongation and, particularly, the so called APL differentiation syndrome are the most serious as they can evolve into severe and potentially fatal ventricular arrhythmias (torsade de points) or respiratory failure, respectively(68-70). The APL differentiation Version 2: May 2008 syndrome (formerly known as retinoic acid syndrome) results from APL cell activation during the differentiation process. It is characterised by fever, dyspnoea, weight gain, pulmonary infiltrates and pleural or pericardial effusion(70). Early recognition of this complication and prompt institution of treatment with high-dose steroids is mandatory because it results in resolution of the syndrome in the vast majority of cases. Severe QT prolongation leading to fatal torsade de points has been reported in patients treated with locally formulated arsenic but never with arsenic trioxide used in clinical trials during post-marketing surveillance(67-69). However, stringent monitoring of serum electrolyte levels (Mg2+, K+) is recommended during therapy with ATO to minimise the risk of severe arrhythmias, particularly in patients receiving concomitant drugs that induce hypokalemia or hypomagnesemia. Other adverse events mentioned above are usually mild and manageable. According to original clinical trials reported from China(54,55), ATO was able to induce hematologic CR in >85% patients who relapsed after front-line ATRA. These results were subsequently reproduced in the USA first in a pilot(56), then in an expanded multicentre trial for patients relapsed after ATRA(58). In the pilot study, hematologic CR was achieved in 91.6% of patients after a median of 33 days of treatment using 10 mg/d as an intravenous infusion(56 ). A CR rate of 86% was reported subsequently in the US multicentre study(58). Significantly, unlike ATRA, ATO as a single agent was able to induce durable molecular remission after two cycles in the majority of patients treated for disease recurrence. Confirmation of the high efficacy of ATO in relapsed APL was provided successively by several trials conducted worldwide which reported CR rates >70% and 1 to 3-year survival rates in the range of 50-70%(57,59-62). Arsenic Trioxide in Combination In addition to trials in which ATO was used a single agent, some studies investigated its efficacy and toxicity profile in combination with other agents including ATRA. Synergism with ATRA and increased anti-leukaemic efficacy in APL was demonstrated in a Chinese randomised study comparing ATO+ATRA vs. either ATO or ATRA used as single agents(71). No significant additional toxicity was reported in this or in other studies which analysed the effect of ATRA and ATO combination( 61,71,72). Following the experience in relapsed patients and based on the favourable toxicity profile, several investigators have more recently explored the effect of ATO in newly diagnosed APL patients and reported preliminary findings in front-line therapy(71-75 ). Results of studies from Shanghai, Houston, India and Iran conducted with ATO as single agent or combined with ATRA for newly diagnosed patients reported CR rates of 86-95%, molecular remission rates after two cycles of 76-100% and survival rates of 86-88%, with significantly better responses being obtained in patients with low and intermediate-risk disease as compared to high-risk patients(71-75 ). Although these data need to be strengthened by studies in larger series and with more prolonged observation, they strongly suggest that at least non-high risk APL patients may be cured without chemotherapy(74). However, this possibility has never been tested in a randomised trial which compares this approach with the current standard ATRA plus chemotherapy front-line therapy. The AML 17 trial will therefore compare the anthracycline approach (AIDA) with the chemotherapy – free ATRA with Arsenic Trioxide combination. The trial is being done in collaboration with the GIMEMA Collaborative Group. Version 2: May 2008 4.4 Molecular Screening and Minimal Residual Disease Monitoring
At diagnosis all cases will have molecular screening. The particular target lesions concern the definition of favourable genetic abnormalities, i.e. AML1-ETO, CBFβ-MYHII and PML-RARα corresponding to t(8;21)(q22;q22), inv(16)(p13q22)/t(16;16)(p13;q22) and t(15;17)(q22;q12-21) respectively. Previous analyses suggest that approximately 15% of cases with these lesions that were not detected by conventional cytogenetics can be detected molecularly. In several cases this was due to technical failure, but may also be explained by more complex rearrangements. Although the number of cases is small they seem to respond in a similar way to cases defined by cytogenetics, and therefore can be used to define the favourable risk group. Recent studies have revealed that 20-27% of AML cases are associated with a mutation of the FLT3 gene, which is an independent prognostic factor. All samples will be sent to the two reference labs (at UCL or Cardiff) will be analysed for FLT3 mutations as a quality control for banked nucleic acid and to establish the mutation status to enable patients to enter the inhibitor randomisation. Samples will be routinely screened for other mutations eg NPM1, CEBPalpha and RAS which in some studies have been shown to have prognostic value (reviewed 76)and will be necessary in evaluating the planned interventions and may contribute to a revised risk score for future treatment choices. Minimal Residual Disease Monitoring
The AML17 trial will provide an opportunity to continue to evaluate and validate
techniques of minimal residual disease monitoring in AML. Within the AML15 trial much
information was collected to define and validate the value of RQ-PCR monitoring in APL
where there is strong evidence and opinion that intervention at the point of molecular
persistence or recurrence is clinically useful, not least because Arsenic Trioxide or
Mylotarg are effective at re-instating molecular negativity. MRD monitoring will be
incorporated as an inherent part of treating patients in the arms of the APL comparison.
Less clear-cut information is available for the Core Binding Factor (CBF) leukaemias.
Considerable information has been collected in serial monitoring in the AML15 trial and
criteria which predict the risk of relapse have been defined. However these criteria have
yet to be prospectively validated. In the case of Core Binding Factor leukaemias, it is far
from clear whether therapeutic intervention at the time these criteria are met, rather than
intervening at the time of relapse, is of benefit. The facility to monitor CBF leukaemias in
patients who enter the AML 17 trial will be available on a commercial basis from the
reference lab in Manchester for those who wish to have the information. Other
molecular lesions e.g. NPM1, may also serve as stable markers of MRD and will, in the
early part of the AML 17 trial, be assessed for its prognostic value with respect to utility
as a marker for molecular monitoring.
A more universal target, is the leukaemia specific immunophenotype which can be
established in over 90% of cases(77). There are now several reports which suggest that
immunophenotypic phenotypes can be characterised in almost all cases of AML and
furthermore the persistence of the phenotype can predict relapse(77). This approach will
also be used in AML17 as an extension of the study already initiated in the AML16 trial.
In the early part of the AML17 trial this approach will be validated in the four reference
labs which have been established for AML16.
Assessment of the Value of Minimal Residual Disease Detection
Version 2: May 2008
Although various techniques have the potential to detect residual disease which predicts
impending relapse, such monitoring requires considerable organisational and technical
resource as well as potential inconvenience and possible anxiety for patients
undergoing serial marrow examinations. It is important to establish whether having this
clinical information improves the patient's prognosis. Apart from the case of Acute
Promyelocytic Leukaemia there is no therapeutic intervention which is of proven value
in the treatment of residual disease. An aim of the AML17 trial is to determine the
clinical value of knowing the MRD status, when detected by any validated method. The
chosen method of doing this, once a validated method has been identified, is to
randomise patients to be monitored or not to be monitored. Within the AML17
protocol non-APL patients who are monitored, and who are thought by the individual
investigator to be at high risk because they have been found to have MRD detected,
can enter the high risk component of the trial.
RANDOMISATION AVAILABILITY

Investigators are invited to regard this protocol as an evolving investigation into AML
treatment. The statistical power calculations differ with each randomisation, so
recruitment to some randomisations may be completed before others. This will mean
that a randomised component of the trial may close or be changed before completion of
the trial as a whole. Similarly, because individual components might require alteration in
the light of trial monitoring or other experience this will be a feature of the trial. It is
possible that for these or other reasons not all of the randomisations will be available at
all times. When such circumstances arise investigators will be informed.
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Studies on treatment of acute promyelocytic leukemia with arsenic trioxide: remission induction, follow-up, and molecular monitoring in 11 newly diagnosed and 47 relapsed acute promyelocytic leukemia patients. Blood 1999; 94: 3315-3324 58. Soignet SL, Frankel SR, Douer D, et al. United States multicenter study of arsenic trioxide in relapsed acute promyelocytic leukemia. J Clin Oncol 2001; 19: 3852-3860. 59. Au WY, Lie AK, Chim CS, et al. Arsenic trioxide in comparison with chemotherapy and bone marrow transplantation for the treatment of relapsed acute promyelocytic leukaemia. Ann Oncol 2003; 14: 752-757 60. Lazo G, Kantarjian H, Estey E, et al. Use of arsenic trioxide (As2O3) in the treatment of patients with acute promyelocytic leukemia: the M.D. Anderson experience. Cancer 2003; 97: 2218-2224 61. Raffoux E, Rousselot P, Poupon J, et al. Combined treatment with arsenic trioxide and all-trans retinoic acid in patients with relapsed acute promyelocytic leukemia. J Clin Oncol 2003; 21: 2326-2334 62. Shigeno K, Naito K, Sahara N, et al. Arsenic trioxide therapy in relapsed or refractory Japanese patients with acute promyelocytic leukemia: updated outcomes of the phase II study and postremission therapies. Int J Hematol 2005; 82:224-229. 63. Shao W, Fanelli M, Ferrara FF, et al. Arsenic trioxide as an inducer of apoptosis and loss of PML/RAR protein in acute promyelocytic leukemia cells. J Natl Cancer Inst 1998; 90: 124-133 64. Miller WH, Schipper HM, Lee JS, et al. Mechanisms of action of arsenic trioxide. Cancer Res 2002 Jul 15; 65. Chou WC, Dang CV. Acute promyelocytic leukemia: recent advances in therapy and molecular basis of response to arsenic therapies. Curr Opin Hematol 2005 Jan; 12(1): 1-6 66. Roboz GJ, Dias S, Lam G, et al. Arsenic trioxide induces dose- and time-dependent apoptosis of endothelium and may exert an antileukemic effect via inhibition of angiogenesis. Blood 2000; 96: 1525-1530 Version 2: May 2008 67. Sanz MA, Lo-Coco F. Arsenic trioxide: Its use in the treatment of acute promyelocytic leukemia. Am J Cancer 2006:5183-191. 68. Unnikrishnan D, Dutcher JP, Varshneya N, et al. Torsades de pointes in 3 patients with acute leukemia treated with arsenic trioxide. Blood 2001 Mar 1; 97(5): 1514-1516 69. Westervelt P, Brown RA, Adkins DR, et al. Sudden death among patients with acute promyelocytic leukemia treated with arsenic trioxide. Blood 2001 Jul 15; 98(2): 266-271 70. Frankel SR, Eardley A, Lauwers G, et al. The ‘retinoic acid syndrome' in acute promyelocytic leukemia. Ann Int Med 1992Aug 15; 117: 292-296 71. Shen ZX, Shi ZZ, Fang J, et al. All-trans retinoic acid/ As2O3 combination yields a high quality remission and survival in newly diagnosed acute promyelocytic leukemia. Proc Natl Acad Sci USA 2004; 101:5328-5335 72. George B, Mathews V, Poonkuzhali B, et al. Treatment of children with newly diagnosed acute promyelocytic leukemia with arsenic trioxide: a single center experience. Leukemia 2004 Oct; 18(10): 1587-1590 73. Ghavamzadeh A, Alimoghaddam K, Ghaffari SH, et al. Treatment of acute promyelocytic leukemia with arsenic trioxide without ATRA and/or chemotherapy. Ann Oncol 2006 Jan; 17(1); 131-134 74. Estey E, Garcia-Manero G, Ferrajoli A, et al. Use of all-trans retinoic acid + arsenic trioxide as an alternative to chemotherapy in untreated acute promyelocytic leukemia. Blood 2006;107:3469-3473. 75.Mathews V, George B, Lakshmi KM, et al. Single agent arsenic trioxide in the treatment of newly diagnosed acute promyelocytic leukemia: durable remissions with minimal toxicity. Blood 2006; 107(7): 2627-2632 76.Mrózek K, Marcucci G, Paschka P, Whitman SP, Bloomfield CD. Clinical relevance of mutations and gene-expression changes in adult acute myeloid leukemia with normal cytogenetics: are we ready for a prognostically prioritized molecular classification? Blood 2007;109:431-48. 77.Freeman SD, Jovanovic JV, Grimwade D. Development of minimal residual disease directed therapy in acute myeloid leukemia. Seminars Oncol 2008, in press. Version 2: May 2008 Section C: PROTOCOL for NON – APL
AML and HIGH RISK
MYELODYSPLASTIC SYNDROME
INCLUSION AND EXCLUSION CRITERIA

Instructions relevant to patients who have Acute Promyelocytic Leukaemia are
given in Section 20 of the protocol.
7.1 Inclusion Criteria Non APL Leukaemia
Patients are eligible for the AML17 trial if: — They have one of the forms of acute myeloid leukaemia as defined by the WHO Classification (Appendix A) — this can be any type of de novo or secondary AML or high risk Myelodysplastic Syndrome (defined as >10% bone marrow blasts). Adult patients with acute promyelocytic leukaemia (APL) are eligible and should be entered into the randomisations specifically for APL (see Section 19). They are considered suitable for intensive chemotherapy. They should normally be under the age of 60, but patients over this age are eligible if intensive therapy is considered a suitable option.  Patients must have liver function tests within twice the upper limit of the normal local range to be eligible for the Mylotarg randomisation.  Women of child-bearing potential (ie women who are pre-menopausal or not surgically sterile) must use acceptable contraceptive methods (abstinence. Intrauterine device (IUD) and must have a negative pregnancy test within 2 weeks of trial entry. Pregnant or nursing patients are excluded. Sexually active men must also use acceptable contraceptive methods They have given written informed consent. 7.2 Exclusion criteria
Patients are not eligible for the AML17 trial if: They have previously received cytotoxic chemotherapy for AML. [Hydroxycarbamide, or similar low-dose therapy, to control the white count prior to initiation of intensive therapy is not an exclusion.] They are in blast transformation of chronic myeloid leukaemia (CML). Version 2: May 2008 They have a concurrent active malignancy. They are pregnant or lactating or taking adequate contraception measures. The physician and patient consider that intensive therapy is not an appropriate
treatment option. (Such patients should be considered for the NCRI AML16
trial for older or less fit patients).
PROCEDURES FOR ENTRY INTO THE TRIAL AND DATA RECORDING

8.1 Centre Registration
Centres will be sent trial information by way of an invitation to participate in the trial.
New regulations on the conduct of clinical trials place obligations on the investigators. In
order to be registered as a trial centre, investigators (as an institution) will be asked to
confirm: (1) that they have received and have read the MRC guidelines for good clinical
practice in clinical trials, (2) that the study has LREC approval, (3) that the institution
has accepted the responsibilities under the Research Governance Framework, (4) that
written consent will be obtained for each patient and a copy retained in the notes, (5)
that they agree to report serious unexpected adverse events as set out in Section 21 of
this protocol, or in any subsequent guidance, (6) that they agree to participate in
random audit carried out by the sponsor or its representative, if requested, (7) that they
will report data in a timely fashion using the internet data collection system, (8) that
material to be stored for research is obtained using the trial consent documentation.
For administrative reasons, investigators will also be asked to confirm that they will
transmit data using the web based data collection system (it is intended to use the
electronic data capture system for trial data collection), and to supply details of the
location of their immunophenotyping, cytogenetic, genetic, pharmacy, tissue typing and
transplant services, and investigator contact e-mail addresses. In addition a limited
amount of biochemical data will be collected and, as part of the centre registration
process, relevant institutional normal ranges (bilirubin, AST, ALT and LDH) will be
recorded.

8.1.1 Patient Recruitment
Patients may be recruited only once a centre is fully registered. Patients should be
consented for overall entry into the trial using Patient Information Sheet 1 and
Consent Form 1. Further consent documents will be used at each randomisation
point. For APL patients see section 19 of the protocol.
8.2 Randomisation
There are four randomisation points in the trial for which contact must be made with the
Wales Cancer Trials Unit (WCTU). Patients fulfilling the criteria for entry into the trial (see
Section 7) should be entered into the first randomisation by telephoning the WCTU in
Cardiff (tel: 02920 196800). Telephone randomisation is available Monday to Friday,
09.00–17.00; internet randomisation is available seven days a week at: website
http://aml17.cardiff.ac.uk
Version 2: May 2008
8.2.1 First randomisation
Note: For this randomisation Patient Information Sheet 2 and Consent Form 2
should be used. During the course of the trial certain randomisation options may
not be available permanently or on a temporary basis. Investigators will be
informed in advance so that only relevant information is given to the patient during
the consent procedure.
Induction chemotherapy allocation will be given once the required patient details
have been supplied. Patients will be allocated to one of the five induction
chemotherapy treatment arms. If patients are ineligible for mylotarg they will be
allocated to the ADE arm.
Arm A; Two courses of ADE
Arm B; Two courses of ADE with Mylotarg 3mg/m2 on day 1 of course 1
or
Arm C Two courses of ADE with Mylotarg 6mg/m2 on day 1 of course 1
or
Arm D: Two courses of DA with Mylotarg 3mg/m2 on day 1 of course 1
or
Arm E: Two courses of DA with Mylotarg 6mg/m2 on day 1 of course 1
Patients have a 20% chance of receiving each of the treatments.
8.2.2 Information required at first randomisation
• Centre and name of consultant in charge of management • Patient's name (family name and given name) • Sex • Date of birth • WHO performance status: o 0=normal activity o 1=restricted activity o 2=in bed <50% waking hours o 3=in bed >50% waking hours o 4=completely disabled. • Type of disease: de novo AML / secondary AML • Whether APL (FAB type M3) or not • Baseline White Blood Count • Confirmation that the patient is eligible for Mylotarg • Confirmation that diagnostic samples of bone marrow and/or blood will be sent to the reference labs for mutation analysis and immunophenotyping. Version 2: May 2008 8.3 Diagnostic material
One objective of the trial is to investigate the therapeutic relevance of new techniques
for detecting minimal residual disease and the quality of remission. Diagnostic material
is essential for these studies. It is of particular importance to define the cytogenetic
abnormalities, and where possible the molecular characteristics, of each patient as this
may be relevant to the treatment strategy.
8.3.1 Cytogenetics and Molecular Genetics

Cytogenetics should be carried out locally and reports sent directly to Professor Christine Harrison/Dr Antony Morman in Newcastle for coding and storage on the central cytogenetic database. To allow risk stratification, cytogenetic results will be required before randomisation at the end of course 1. Cell pellets should be stored locally. If there are difficulties locally, central facilities will be provided by Mrs Yashma Patel at UCH — please indicate clearly on the samples that cytogenetic analysis is required. Professor Harrison will coordinate cytogenetics in children.
8.3.2 FLT3 Mutation Status
Molecular definition is intended for all patients, initially for characterisation of FLT3 mutation, for identification of cases with cryptic gene rearrangements that reassign patients to the favourable risk group, and for the identification of cases suitable for minimal residual disease monitoring. To enable this to be achieved in the timescale required samples should be sent to either Dr P White in Cardiff or Professor R Gale at University College Hospital using the dispatch methods currently in place. Investigators will be informed of the FLT3 mutation status of patients to determine eligibility for the FLT3 inhibition randomisation. Additionally, they will be told of patients in whom molecular screening alters the risk group assignment. All cases of AML will be candidates for MRD assessment using one of a range of targets and separate paired marrow and blood samples should be routinely sent following induction to Prof. Grimwade/Professor Yin (molecular markers) and to the relevant reference immunophenotyping centre (see Section 15). FLT3 mutation analysis will be analysed in real time at two reference laboratories
(see below). Diagnostic material will also be stored for studies of resistance
proteins, WT-1 gene expression, DNA microarray and future research studies, for
which patient informed consent must be obtained (use Patient Information Sheet 9
and Consent Form 9). Molecular screening will be carried out in the reference
molecular labs.
It is essential that a sample is sent to a designated laboratory for the
identification of patients with a FLT3 mutation. These laboratories will pass
samples on to the laboratories designated for MRD monitoring. It is intended that
investigators will have the results of FLT3 assays by the end of the first course of
chemotherapy to enable eligible patients to be randomised between FLT3 inhibition
and not.
Laboratories for FLT3 Mutation Analysis and Molecular Screening:
Department of Haematology, University College Hospital, London. Version 2: May 2008 (Professor R Gale)
Department of Haematology, University Hospital of Wales, Cardiff
(Dr P White)
Samples at diagnosis for molecular analysis:
4 ml of bone marrow and 30ml of blood in EDTA.
(To be sent to UCL or Cardiff Labs)
Samples at diagnosis for cytogenetic analysis (local labs):
4 ml of bone marrow in tissue culture medium with preservative-free heparin 30 ml of heparinised blood Ideally, both marrow and blood should be sent, but if only one is available please send that. 8.3.4 Immunophenotyping
Immunological definition is essential and a diagnostic bone marrow and blood sample
should be sent to the designated reference laboratory in order to establish the leukaemia
associated aberrant immunophenotype (LAIP) as a target for subsequent MRD
monitoring. This involves the use of standardised methodology with an extended range of
antibody panels and hence this information cannot be provided by non-designated labs.

.
Laboratories for Immunophenotypic Characterisation and Monitoring:
Dr Sylvie Freeman Clinical Immunology Department of Immunology Division of Infection and Immunity Southmead Hospital University of Birmingham Westbury on Trym Tel: 0117 9596306 Birmingham, B15 2SZ Fax: 0177 959 6062 Tel: 01214158759 Mob: 07884310528 E-mail: [email protected] Fax: 01214143069 [email protected] Mr Steve Couzens Dr Christopher McNamara Department of Haematology Haematology Department University Hospital of Wales Royal Free Hospital Heath Park, Cardiff Tel: 02920742370 Fax : 02920745084 Tel: Tel: 0207 794 0500 e-mail: [email protected] Fax: 020 7830 2313
Arrangements will be made to allocate individual sites to one of these labs
Version 2: May 2008 8.3.5 Follow-up Material
All patients should be considered eligible for MRD monitoring. At diagnosis
Investigators should send one molecular sample to Cardiff or UCL and the
immunophenotyping sample to one of the four reference labs. Sites will be
informed of which labs they should associate with.
The majority of non-APL patients will have a molecular and immunophenotypic
marker, potentially allowing more accurate assessment of remission status following
Course 1. Results of these analyses may ultimately enhance the risk score and be
used to inform risk stratification later in the trial. Therefore separate paired marrow
and blood samples should be routinely sent on regeneration following induction to
the relevant reference immunophenotyping lab (see above) and to Prof Yin or Prof
Grimwade for detection of molecular markers (see section 11.4 & 20.10 for
addresses). Clinicians will be informed if their patient is most appropriately
monitored by immunophenotyping or a molecular marker and the laboratory to
which subsequent MRD samples should be sent. Arrangements for monitoring
these patients are set out in Section 15. The labs undertaking initial characterisation
and MRD are listed above.
The immunophenotyping labs are not providing a diagnostic service under these
arrangements.
8.4 Data recording
It is intended to develop data recording for this trial as a web-based system. This is a secure encrypted system accessed by an institutional password, and complies with Data Protection Act standards. The system can be accessed on: A user password will be supplied to investigators on receipt of the letters of LREC approval and site specific assessment, and centre registration information (see Section 8.1). Investigators who do not wish to use the internet system should make arrangements with the trial centre in Cardiff. Web based data collection forms should be completed as follows: Notification of Entry (Form A) — return when all the diagnostic data requested are
available (but not later than 1 month after entry).
Induction Chemotherapy (Form B) — return when blood counts have recovered after
the second induction course, or at prior death (but not later than 2 months after
completion of Course 2).
Consolidation Chemotherapy (Form C) — return when blood counts have recovered
after the final course of consolidation chemotherapy, or at prior death (but not later than
2 months after the final course).
Version 2: May 2008
Molecular Inhibition (Form D)  return for patients allocated to receive either FLT3
or mTOR inhibitor
Transplant (Form E only for patients receiving a transplant) — return when blood
counts have recovered post transplant, or at prior death (but not later than 3 months
after transplant).
One Year Follow-up (Form F) — return at one year after the end of treatment in 1st CR
(i.e. last consolidation chemotherapy or transplant), or at death if the patient dies within
1 year of finishing therapy.
Relapse (Form G) — return at the completion of reinduction (and consolidation)
therapy or at death (but not later than 4 months after relapse).
8.5 Health Economics
Basic information on resource usage will be collected in the data forms B to G on all patients. Selected patients will be invited to provide additional information in the form of a patient diary that will be issued to the patient by the investigator. Once a patient has been randomised, it is very important to have full details of the subsequent course of events, even if allocated therapy has been abandoned. Although clinical decisions remain with the physician (see Section 1, Ethical Considerations), follow-up data must continue to be collected on such patients and trial forms must be filled in, as far as possible, giving details of the therapy actually received and its outcome. INDUCTION CHEMOTHERAPY: Courses 1 and 2

Each induction schedule comprises two courses of allocated chemotherapy. Remission
status will be determined after each course. After Course 1, the additional or alternative
treatments will be decided as patients are characterised as having Core Binding Factor
leukaemia, the presence of a FLT3 mutation, a high risk score, or none of these. The
additional interventions are described in section 11 of the protocol. If a patient is not in
complete remission after course 2, they may enter the high risk randomisation (section 11.5).
9.1 ADE schedule
ADE 10+3+5
Cytosine Arabinoside 100 mg/m2 12-hourly by i.v. push on days 1-10 inclusive (20 doses). Daunorubicin 50 mg/m2 daily by slow (1 hour) i.v. infusion on days 1, 3 and 5 (3 doses). Etoposide 100 mg/m2 daily by 1 hour i.v. infusion on days 1-5 inclusive (5 doses). ADE 8+3+5
Version 2: May 2008 Cytosine Arabinoside 100 mg/m2 12-hourly by i.v. push on days 1-8 inclusive (16 doses). Daunorubicin 50 mg/m2 daily by slow (1 hour) i.v. infusion on days 1, 3 and 5 (3 doses). Etoposide 100 mg/m2 daily by 1 hour i.v. infusion on days 1-5 inclusive (5 doses). 9.2 DA schedule
Daunorubicin 50 mg/m2 daily by slow (1 hour) i.v. infusion on days 1, 3 and 5 (3 doses). Cytosine Arabinoside 100 mg/m2 12-hourly by i.v. push on days 1-10 inclusive (20 doses). Daunorubicin 50 mg/m2 daily by slow (1 hour) i.v. infusion on days 1, 3 and 5 (3 doses). Cytosine Arabinoside 100 mg/m2 12-hourly by i.v. push on days 1-8 inclusive (16 doses). 9.3 Administration of Mylotarg
Patients allocated to receive Mylotarg must not have a white count greater than 30 x
109/L at the time of Mylotarg administration because of the risk of tumour lysis. Such
patients should either have the WBC reduced with Hydroxycarbamide before
commencing trial chemotherapy or have the administration of Mylotarg delayed until
day 4 of the chemotherapy. Patients are only eligible to receive Mylotarg if the liver
function tests do not exceed twice the upper limit of the normal range in the local
laboratory.

Mylotarg will be given at a dose of 3 mg/m2 or 6 mg/m2 on day 1 of Course 1. Details
of the premedication, and other procedures for Mylotarg administration, are set out in
Appendix B.

ASSESSMENT OF RESPONSE
A bone marrow aspirate to assess remission status should be carried out at 18-21 days after the end of Course 1. If the bone marrow is of adequate cellularity for the assessment of haematopoiesis, the patient's remission status should be ascertained. If the marrow is hypoplastic and assessment of status is not possible, a repeat marrow should be performed after a further 7-10 days and remission status be assessed. The level and date of the maximum level of neutrophil and platelet recovery should be recorded. In order to achieve a subsidiary aim of the trial (i.e. assessing the relevance of residual cytogenetic or molecular existence of disease in morphological CR) investigators should Version 2: May 2008 also request cytogenetic analysis on this sample. In addition a paired marrow and blood sample should be sent to the relevant reference immunophenotyping laboratory and a separate paired sample to Prof Yin or Prof Grimwade for molecular assessment of MRD (see Sections 8.3.4, 11.4 and 20.10 for addresses) 10.1 Definitions of Complete Remission, Partial Remission and Resistant Disease

Complete Remission (CR): The bone marrow is regenerating normal haemopoietic
cells and contains <5% blast cells by morphology in an aspirate sample with at least
200 nucleated cells. Additionally there is an absolute neutrophil count of more than
1000/µL and platelet count of at least 100,000/µL
Complete Remission with incomplete recovery (CRi): Fulfilling all criteria for CR
except for residual neutropenia (<1000/µL) or thrombocytopenia (<100,000/µL)
Partial Remission (PR): The bone marrow is regenerating normal haemopoietic cells
and blast count has reduced by at least half, to a value between 5 and 25% leukaemic
cells.
Resistant Disease (RD): The bone marrow shows persistent AML, and patient survives
at least 7 days beyond end of course.
Once blood counts have recovered after the second course of induction therapy, the completed "Induction Chemotherapy" form (Section B) should be completed on the web-based data collection system. Version 2: May 2008 ADDITIONAL TREATMENTS
11.1 Immediately after the completion of chemotherapy patients become eligible for additional or alternative treatment. Within 10 days of entering the trial the
reference labs will have defined the FLT3 mutation status. If a mutation is found
the site Principal Investigator (PI) and research nurses will be informed thus
enabling the patient to enter the FLT3 Inhibitor randomisation (Section 11.3).
After recovery of blood counts and marrow assessment of response additional
information will be available. Patients with Core Binding Factor Leukaemias will be
identified and sufficient information will be available to calculate the individual
patient's risk score. The investigator will be informed if the patient has a high risk
score, and that the patient should therefore enter the high risk treatment options
(Section 11.5). Patients who are in none of these categories are eligible for the
addition of mTOR inhibition (Section 11.6), which will start after course 2. The
computer randomisation system will identify which randomisation patients are
eligible to enter (by calculating risk score and identifying patients who are either
CBF or have a FLT3 mutation).
Patients in these randomisations will be randomised in a 2:1 fashion, so that there is a two out of three chance of receiving either mTOR or FLT3 inhibitor or Daunorubicin/Clofarabine in the high risk option. 11.2 Patient Information and Consent

Additional consent will be required for the additional treatments:
For patients eligible for FLT3 Inhibition use Patient Information Sheet 4 and
Consent Form 4
For patients eligible for the high risk treatments use Patient Information Sheet 5 and
Consent Form 5
For patients eligible for mTOR inhibition use Patient Information Sheet 6 and
Consent Form 6
11.3 FLT3 INHIBITION

Patients who have a confirmed FLT3 mutation are eligible to enter the FLT-3
inhibition randomisation. Patient Information Form 4 and Consent Form 4
should be used. Patients should be randomised immediately following the end of
the first course of chemotherapy. Patients will be randomised to receive CEP-701
in a 2:1 fashion and will commence treatment 2 days after the completion of
each course of chemotherapy and should continue until two days before the
commencement of the next chemotherapy course, or for a maximum of 28 days
after the end of the chemotherapy course. CEP-701 should not be administered
concurrently with other chemotherapy. Patients allocated to inhibitor are intended
to receive CEP-701 for four courses, each of up to 28 days in duration, between
allocated chemotherapy. It is expected that CEP-701 will be administered at
Version 2: May 2008 home, and investigators must ensure that the patient has received adequate
instruction in reconstituting the drug. An instruction sheet is given in Appendix D
and is available on the trial website (website http://aml17.cardiff.ac.uk).
The CEP-701 randomisation should take place as soon as the FLT3 status is known, so that drug supplies can be put in place and so that treatment can start 2 days after completion of the allocated chemotherapy. Investigators are advised to discuss the possibility of randomisation to CEP-701 with the patient before initial entry to the trial, and before mutation status is known. Randomisation should take place irrespective of disease response. To randomise a patient, (i) telephone the WCTU (tel: 02920 196800) during office
hours (09:00 to 17:00 hrs, Monday to Friday); or (ii) use the 24 hour internet
randomisation available at: website http://aml17.cardiff.ac.uk
Before treatment allocation is given, investigators will need to provide: • The name and hospital of the randomising clinician • The AML17 trial number (or full name and date of birth) • The approved laboratory where mutation analysis was done • Confirmation of the patient's FLT3/ITD mutation status • Date of completion of the first course of chemotherapy • Whether or not the patient is receiving prophylactic azole anti-fungal treatment.
11.3.1 CEP-701 TREATMENT
Patients randomised to chemotherapy plus sequential CEP-701 will receive a dose of
80 mg bd starting 2 days after the last administration of each course of induction
chemotherapy. Note: because of a likely interaction with azole antifungal agents,
where the patient is to be treated with azoles, the initial CEP-701 dose should be
40mg bd, for the first 7 days of each course of treatment to avoid gastrointestinal
symptoms, if tolerated the dose can be continued at 60mg bd. If it emerges that
the patient cannot tolerate the 60mg dose they should continue on 40mg.
Investigators may have to continue to adjust the dose based on the patient's
symptoms
Under no circumstances should CEP-701 be co administered with any course of
chemotherapy treatment.

Treatment will be given daily for up to 28 days or until 2 days before the next course of
chemotherapy, whichever is sooner. When subsequent courses of chemotherapy are
given, treatment with CEP-701 must stop 2 days before the first administration of the
next course of chemotherapy, because elevated CEP-701 plasma concentrations may
interfere with the effect of chemotherapy. Treatment with CEP-701 will recommence
2 days after the last administration of chemotherapy in the subsequent courses. In
patients who are allocated to receive one course of consolidation treatment (see section
12 for details) the fourth course of CEP-701 should be commenced 7 days after the
completion of the 28 days of CEP-701 given after consolidation course 1.
Version 2: May 2008

Patients randomised to receive chemotherapy plus sequential CEP-701 who have not
achieved complete remission after the second course of chemotherapy will discontinue
the study. After patients have completed two courses of induction treatment those in CR
will be expected to enter the consolidation randomisation as described in sections 12
and 13.

11.3.2 Dose Adjustment

In patients who are not receiving azole anti-fungals the dose of CEP-701 may be
reduced to 60 mg bd at any time for any patient receiving CEP-701 if the 80 mg bd
dosage is not well tolerated; a return to 80 mg bd is permitted if tolerance improves. The
dose may be increased to 100 mg bd under the following circumstances:
•
Where patients have tolerated CEP-701 treatment at 80 mg bd well and have met the criteria for a second course of chemotherapy. (CEP-701 may be administered at 100 mg bd following completion of the second course of chemotherapy.) Where patients have tolerated CEP-701 treatment at 80 mg bd well and have achieved at least a PR, CEP-701 may be administered at 100 mg bd after the marrow assessment), In both cases, the dosage of CEP-701 treatment must be reduced to 80 mg bd (and if
necessary 60 mg bd) in the event of poor tolerability.
In patients who are receiving azole anti-fungals the dose of CEP-701 should
commence at 40 mg bd for the first 7 days of each treatment course. If well tolerated the
dose can be increased thereafter to 60mg bd. If the 60mg dose is well tolerated the
80mg dose can be attempted, but if the 60mg dose is not well tolerated the patient
should continue at the 40mg dose. Investigators are requested to record the sequence
of dosing administered on the appropriate data collection form (Form D).
The dose can be increased to 100 mg bd under the following circumstances:
•
Where patients have tolerated CEP-701 treatment at 80 mg bd well and have met the criteria for a second course of chemotherapy. (CEP-701 may be administered at 100 mg bd following completion of the second course of chemotherapy.) Where patients have tolerated CEP-701 treatment at 80 mg bd well and have achieved at least a PR, CEP-701 may be administered at 100 mg bd after the marrow assessment.) The most likely side effect associated with CEP-701 treatment is nausea, so patients should be given precautionary anti-emetic treatment. CEP-701 is supplied in 100 ml glass bottles as a clear yellow oral solution at a concentration of 25 mg/ml in polysorbate 80 NF (10 ml) and propylene glycol USP (10 ml). Prior to administration, CEP-701 should be diluted in fruit juice. The following juices are approved for use to administer CEP-701: Version 2: May 2008 • V8® 100% vegetable juice • orange juice (pulp-free) During the study, patients will receive multidose bottles, each containing 100 ml of CEP-701 solution, from the investigator. Patients must be formally assessed on or near day 14 of CEP-701 treatment, and issued with further supplies as required. At each visit, patients should return all used and unused bottles to monitor dosage and compliance. Appendix D gives the dosing regimen. Patients who are being treated with CEP-701 should be reviewed on or as near as possible to day 14 from the start of CEP-701 treatment. They should be evaluated for drug tolerance and a dose adjustment made if required. At the day 14 assessment, 20ml of blood should be collected and sent to the Cardiff laboratory in a standard lithium heparin container, using the Royal Mail collection service provided, for the assessment of free CEP-701 and FLT3 inhibitory activity and azole blood levels. 11.4 CORE BINDING FACTOR LEUKAEMIA
Patients who have Core Binding Factor leukaemias, t(8;21)/AML1-ETO and inv(16)/t(16;16)/CBFB-MYH11, will continue with the chemotherapy as allocated for course 2 which will include Mylotarg for those patients who were not allocated to receive it in course 1. Samples of bone marrow and blood at time of routine assessment for remission should be sent to the molecular laboratory in Manchester who can provide information on the patient's molecular response. Core Binding Factor Leukaemia minimal residual disease monitoring is not part of the formal assessment of the value of minimal residual disease monitoring being evaluated in the trial. This information can be provided on a commercial basis by arrangement with the Manchester lab : contact details below: Laboratory for Core Binding Factor Leukaemia Molecular Monitoring:

Molecular Diagnostics Centre Department of Haematology Top Floor, Multi-purpose Building Manchester Royal Infirmary Manchester Royal Infirmary Tel: 0161 276 4802 (direct to Sec) Tel: 0161 276 4137 Fax: 0161 276 4814 Fax: 0161 276 4814 Email: [email protected] Email: abida.Anwan @cmmc.nhs.uk Version 2: May 2008 It is recognised that a small number of Core Binding Factor Leukaemias will already have entered the FLT3 inhibitor randomisation before the cytogenetic information was available. These patients should continue in the FLT3 assessment and should continue to receive the inhibitor if allocated. If they had been allocated to ADE in course 1,they should also receive Mylotarg (3mg/m2 or 6mg/m2) on day 1 of course 2. 11.5 HIGH RISK SCORE PATIENTS.
After course 1, sufficient information will be available to assign a risk score to individual
patients. This is based on age, de novo or secondary disease, cytogenetics, white blood
count, sex and response to course 1. This will be allocated by providing the required
information to the trial office/internet system. The additional information required, in addition
to what was provided in Form A is the cytogenetic result and marrow response after course
1.
N.B. Treatment of patients with Core Binding Factor leukaemias or who have a FLT3
mutation, is not influenced by the risk score, and risk score is not required for such
patients.
Patients who are defined as high risk will enter the high risk treatment randomisation with the
expectation that they should proceed to transplantation
The standard arm in this patient group is FLAG-Ida. Patients will be randomised to treatment
in a 1:2: manner, so the chance of receiving the standard arm (FLAG-Ida) is 1 in 3, and of
receiving the novel combination of Daunorubicin/Clofarabine 2 in 3. For entry into this
randomisation Patient Information Sheet 5 and Consent Form 5 should be used. The
treatments are:

Up to three courses of FLAG-Ida [standard arm]
Up to three Courses of Daunorubicin/Clofarabine

FLAG-Ida:
Fludarabine 30 mg/m2 daily by 30-minute i.v infusion on days 2-6 inclusive (5 doses). Cytosine Arabinoside 2 g/m2 daily over 4 hours starting 4 hours after Fludarabine on days 2-6 inclusive (5 doses). G-CSF [Lenograstim 263µg (1 vial)] s.c. daily days 1-7 inclusive (7 doses). Idarubicin 8 mg/m2 i.v. daily on days 4, 5 and 6 (3 doses). Patients should receive up to 3 courses of FLAG-Ida but should proceed to transplant
as soon as practical if the option is available.

Daunorubicin/Clofarabine:

Course 1
Daunorubicin 50 mg/m2 daily by i.v. infusion on days 1, 3 and 5 (3 doses). Version 2: May 2008 Clofarabine 20mg/m2 by i.v. infusion over 1 hour daily on days 1 to 5 Daunorubicin 50 mg/m2 daily by i.v. infusion on days 1, 3 and 5 (3 doses). Clofarabine 20mg/m2 by i.v. infusion over 1 hour daily on days 1 to 5.
The main side effect of Clofarabine will be myelosuppression, which can be quite
variable in duration. It is therefore recommended that if patients whose marrow is
cleared of blast cells, but have failed to regenerate neutrophils to 1x109/l by day 32 from
the end of treatment (by which time 95% of patients on standard treatment would have
regenerated), should have the dose of Clofarabine in course 2 reduced to 15 mg/m2
daily for 5 days. Patients who enter the Clofarabine randomisation are required to have
a serum creatinine within the normal range. Serum creatinine should also be measured
on each treatment day and the Clofarabine withheld if the level rises above the upper
limit of normal. Patients should be well hydrated during Clofarabine treatment.
In light of new observations blood products for patients receiving Clofarabine
should be irradiated

Patients who are at high risk are recommended to receive an allogeneic transplant from a
matched sibling or volunteer donor either with standard or reduced intensity conditioning.
However it is recognised that it takes time for the arrangements for transplant to be made,
and that there will be a number of patients for who a donor cannot be identified. Therefore
patients should continue with the allocated treatment courses until the transplant can be
delivered. It is recommended that patients in whom a reduced intensity allograft is intended
should receive a minimum of two high risk treatment courses.
11.6 mTOR Inhibition - Everolimus
Patients who do not have Core Binding Factor Leukaemia, a FLT3 mutation, or a High Risk
Score are eligible to enter a randomisation to receive or not the mTOR inhibitor Everolimus
(in a 2:1 ratio). This will be given as a daily oral dose of 10mgs starting 2 days after the end
on each chemotherapy course for up to 28 days or until 2 days before the next course is
initiated, which ever is shorter. If patients are allocated to receive 3 courses of chemotherapy
in total they should have a fourth course of Everolimus after a break of one week, and the
treatment should continue for 28 days. Patients entering the mTOR randomisation should
use Patient Information Sheet 6 and Consent Sheet 6
Patients may be requested to provide a 10ml sample of peripheral blood immediately before each treatment course and on day 14 of each course. Reminders will be sent to investigators where this is required. The side effect profile of Everolimus is described in Appendix B. It should be noted that hyperlipidaemia and hyperglycaemia may occur and these levels should be monitored after each course, ie immediately before the next chemotherapy course. 11.6.1 Dose De-escalation
Version 2: May 2008 If patients have side effects which are thought to be due to the administration of Everolimus, the subsequent dose can be omitted or reduced by 50% by dosing on alternate days. If the 50% dose reduction is not tolerated, subsequent doses should be omitted 11.7. Progression Through Induction Therapy
FLT3 mutation status should be available by the end of the first course of chemotherapy, (see Section 10). After recovery from course 1 and assessment of response, the risk score can be provided for individual patients who are not already in the CEP-701 randomisation or with Core Binding Factor Leukaemia. Those with high risk disease should enter the randomisation detailed in Section 11.5. All except the high risk or refractory patients should receive the second chemotherapy course. The marrow should be re-assessed at 18-21 days after the end of Course 2 for the assessment of morphological, immunophenotypic and molecular response. After Course 2, when patients in complete remission have regenerated to 1.0 x 109/l neutrophils and 100 x 109/l platelets, they are ready for the consolidation randomisation (see Section 12) and commencement of consolidation treatment, i.e. Course 3 (see Section 12) For patients who are not in complete remission after Course 2 treatment will be deemed to have failed. They may be entered into the high risk arm or withdrawn from the trial and treated at the investigator's discretion. All patients off protocol will still continue to be followed up within AML17. Patients who have been allocated to receive an inhibitor should continue to receive the inhibitor irrespective of which consolidation chemotherapy arm is allocated 12 CONSOLIDATION RANDOMISATION

Note: For this randomisation Patient Information Sheet 7 and Consent Form 7 should
be used.
12.1 Randomisation Options
The consolidation randomisation is available to patients who have achieved complete
remission within 2 courses and are not candidates for the high risk score randomisation.
The randomisation is to one (course 3) or two (courses 3 and 4) courses of consolidation
treatment. The treatment to be used is the MRC consolidation (MACE/MidAC). Patients
allocated to one course will receive MACE and those allocated to two courses will receive
MACE followed by MidAC. Patients who have already been allocated to receive FLT3 or
mTOR inhibition will continue with that treatment as well.

12.2 Timing of Consolidation Randomisation
Statistically, it is preferable for the randomisation to take place as close as possible to the start of consolidation course 1 (Course 3). This will reduce non-compliance, which would have an adverse impact on the power of the trial. Although randomisation should be carried out as close to Course 3 as possible, it is recommended that the options available are discussed with the patient at an earlier Version 2: May 2008 stage, e.g. during induction therapy, in order to ensure that the patient has plenty of time to consider the options and arrive at an informed decision. This should reduce the risk of non-compliance with allocated treatment. 12.3 Information Required at Consolidation Randomisation
Before carrying out the consolidation randomisation please make sure that: (a) The patient is in complete remission (b) The patient's risk group is known. (c) It has been decided whether the patient is willing to be randomised between MACE or MACE and MidAC consolidation chemotherapy. For randomisation: (i) telephone the WCTU (tel: 02920 196800) during office hours
(09:00 to 17:00 hrs, Monday to Friday); or (ii) use the 24 hour internet randomisation
available at: website http://aml17.cardiff.ac.uk
Treatment allocation will be given once the following patient details have been supplied: • AML17 trial number (or full name and date of birth). Confirmation that the patient has received two courses of induction therapy, and is currently in complete remission. The patient is not high risk • Whether the patient is to be randomised between one and two additional courses (if not the patient should receive 2 more courses). Whether already enrolled in the FLT3 or mTOR inhibitor randomisations. 13 CONSOLIDATION CHEMOTHERAPY: Courses 3 and 4
Consolidation schedule comprises one or two courses of chemotherapy. If allocated to one course on the MRC arm, the patient will receive the MACE treatment. Patients who do not wish to be randomised for the consolidation options should be allocated to receive both MACE and MidAc courses. 13.1 MRC Consolidation

Course 3
Amsacrine 100 mg/m2 daily by 1 hour i.v. infusion (in 5% dextrose) on days 1-5 inclusive (5 doses). Cytosine Arabinoside 200 mg/m2 daily by continuous i.v. infusion on days 1-5 inclusive. Etoposide 100 mg/m2 daily by 1 hour i.v. infusion on days 1-5 inclusive (5 doses). Version 2: May 2008 Note: Amsacrine must not be infused in 0.9% sodium chloride: precipitation or
flocculation occurs. This will necessitate a 2-hour interruption of the Cytosine
Arabinoside infusion.
Where venous access is limited to a single lumen line a 2 hour interruption to the Ara-C
infusion may be required to enable the Amsacrine and Etoposide administration.
Course 4
Mitoxantrone 10 mg/m2 daily by slow (1 hour) i.v. infusion on days 1-5 inclusive (5 doses). Cytosine Arabinoside 1.0 g/m2 12-hourly by 2-hour i.v. infusion on days 1-3 inclusive (6 doses). NB. If a patient is randomised to receive one consolidation course they should
receive MACE

Course 4 should ideally be given once counts have recovered to 1.0 x 109/l neutrophils and 100 x 109/l platelets following Course 3. Delay in count recovery regularly occurs, and problem cases should be discussed with the clinical coordinators. Once blood counts have recovered after the fourth course of chemotherapy, the "Consolidation" form (Form C) on the web based data collection system should be completed. Patients who have entered the FLT3 inhibitor or mTOR randomisation, and who have
been allocated CEP-701 or Everolimus respectively, should receive the drug after
courses 3 and 4 as described in sections 11.3 and 11.6.


14. STEM CELL TRANSPLANTATION
The protocol provides for allogeneic transplantation for all adult patients who have an HLA-matched sibling or volunteer unrelated donor and who are designated to have a high risk score. As soon as a potential donor is identified the transplant centre should be informed. The transplant should be carried out 6-8 weeks after the final course of chemotherapy. The type of transplant and the transplant protocol will be determined by the transplant centre's usual policy. As a guide based on prior evidence: 1. Patients <35 years should receive a conventional allogeneic transplant with Cyclophosphamide and Total Body Irradiation (8 x 180cGy fractions). 2. Patients 35-44 years can receive a conventional allogeneic transplant or a reduced intensity allograft depending on investigator or patient choice. 3. Patients ≥45 years should receive a "mini" allograft. Version 2: May 2008 14.1 Conventional Allogeneic Transplantation
If the patient meets the criteria of the transplant centre, he/she will receive the transplant as soon as is practical. It is expected that they will have received one or two of the allocated treatment courses in the high risk arm. The most widely used myeloablative schedule is Cyclophosphamide and Total Body Irradiation (8 x 180 cGy). The source of stem cells can be bone marrow or peripheral blood. If peripheral blood is used, a dose of at least 4 x 106 CD34 cells/kg should be given. Graft versus host prophylaxis will be determined by the transplant centre, but the most widely used is Methotrexate and Cyclosporin. It is required that patients who receive a transplant will provide written consent in line with the transplant centre policy. 14.2 Reduced Intensity Allograft
Patients who will receive a reduced intensity allograft must first receive two courses of
the high risk arm and the mini-allograft as Course 4. The mini-allograft should only be
carried out at centres with experience of this approach and should not be carried out
in centres who do not perform conventional allografts. The precise protocol to be
used in the AML17 trial will be that chosen by the transplant centre, but may be subject
to change in light of emerging evidence in the field.
Transplant centres initially may wish to choose one of two reduced intensity protocols:
FBC Protocol:
days –9 to –5 inclusive days –3 and –2 days –5 to –1 inclusive (use of phenytoin and low molecular weight heparin for VOD prophylaxis is
Fludara, Melphalan, Campath (UCL) Protocol:
days –7 to –3 inclusive Campath 1H 20 mg/day days –8 to –4 inclusive Since patient and donor will require time to be counselled about the transplant option which may be delivered as early as course 3, investigators are encouraged to identify donor availability as soon as possible after diagnosis. Collection of Autologous stem cells is not an inherent part of the AML17 trial but nor is it proscribed. On completion of the transplant the "Transplant" form (Form E) should be completed via the web-based system. 15. ARRANGEMENTS FOR MOLECULAR SCREENING AND MINIMAL RESIDUAL
DISEASE MONITORING
15.1 Molecular Screening
All diagnostic material will be collected into the MRC AML tissue bank at the UCL
(Professor R Gale) or Cardiff (Dr P White) Labs, from where it will immediately be
analysed for FLT3 status and subsequent molecular screening and also stored for
Version 2: May 2008 future research. Investigators should note that patients' consent must be given for this
donation, and documentation concerning this is included in the main trial consent
documentation (Patient Information Sheet 9 and Consent Form 9). Molecular
screening for the more common mutations is intended on all patients. The banking
facilities at UCL and Cardiff are licensed under the Human Tissue Act. The reference
labs do not require to have a copy of the consent documentation but are working on the
assumption that the sending of the sample constitutes consent. It is the responsibility of
the investigator to ensure that when excess sample is sent that consent has been
obtained. If this is not the case the reference labs must be informed to enable the
sample to be destroyed.
These labs will undertake the FLT3 mutation assessment to enable entry into the FLT3
inhibitor randomisation. Samples will also be assessed for in vitro sensitivity to CEP-
701.

Laboratory Contacts:

Department of Haematology Cancer Institute, Department of Cardiff University School of Paul O'Gorman Building University College London 72 Huntley Street Tel: 02920 742375 Fax: 02920 744655
15.2 Minimal Residual Disease Monitoring
A major question to be addressed in the AML17 trial is the clinical value of disease
monitoring using molecular and immunophenotypic approaches. The referred sample to
UCL or Cardiff will identify patients who are candidates for molecular monitoring of
MRD. In patients consenting to MRD assessment, paired marrow and blood samples
should be sent following each course of chemotherapy. Post-induction samples from all
non-APL patients should be sent to Professor Yin in Manchester to assess WT1
response and other appropriate markers (in addition a separate paired marrow and
blood sample should be sent to the designated immunophenotyping lab, see Sections 8
and 10). After induction, investigators will be informed which markers are relevant in
their patients and subsequent samples should be sent to the appropriate lab i.e. to
Manchester for CBF leukaemia and WT1 and to Professor Grimwade in London for
cases with NPM1 mutation. Investigators will receive requests for further follow up
samples in relevant patients who have given consent to be monitored.
Version 2: May 2008 NPM1
Dr Abida Awan/Prof Yin Prof David Grimwade Molecular Diagnostics Centre Department of Medical & Molecular Genetics Top Floor, Multi-purpose Building 8th Floor, Tower Wing Manchester Royal Infirmary Tel: 0207 188 3699 (lab) Tel: 0161 276 4137 Fax: 0207 188 2585 Fax: 0161 276 4814 Email: [email protected] Email: abida.Awan @cmmc.nhs.uk Samples from children for MRD monitoring should be sent to their local MRD laboratory for appropriate forwarding to other laboratories. These are listed below: Bristol Children's Hospital Department of Haematology North Trent Molecular Genetics Haematology and Bone Marrow Royal Hospital for Sick Children Sheffield Children's Hospital Transplant Research Group Dept of Pathology and School of Medical Sciences, Tel: 0141 201 0689 Tel: 0114 271 7003 University of Bristol, Fax: 0141 201 0857 Fax : 0114 273 7467 Tel: 0117 928 9158/7888
Fax: 0117 928 7896


15.3 Frequency of Molecular Monitoring

On entering AML17, it should be explained to patients that their leukaemia cells are
likely to have an appropriate target for minimal residual disease monitoring and will
be invited to participate in this aspect of the trial. The WT1 gene is over-expressed
in over 80% of AML cases. Investigators will be alerted by the molecular monitoring
group (Professor Grimwade or Tissue Co-ordinator), should any additional markers
be identified and follow-up samples should be sent to the appropriate lab as
detailed above (Section 15.2). Since in patients with APL the strategy of treatment
reduction is being tested, molecular monitoring is an inherent part of the APL
treatment. In the non-APL patients the intention is routinely to monitor blood and
bone marrow after each course of chemotherapy, and at regular intervals (3-4
monthly) until 3 years following consolidation, to establish the most appropriate
monitoring schedule for any given target. Monitoring of Core Binding Factor
Leukaemia will be available from the reference lab in Manchester, but is not being
evaluated in the clinical evaluation of disease monitoring as described in section
15.5.The frequency of monitoring may change during the trial as new information or
new markers becomes available. Since it has become clear that persistent MRD or
molecular relapse with rising transcript level powerfully predicts relapse, it is
important to ensure that the test is completely reliable for that patient. This may
result in advice to repeat the test within the interval planned. The issue of sequential
testing is incorporated in the Patient Information Sheet 9 and Consent Sheets 9.
Version 2: May 2008 15.4 Monitoring by Immunophenotyping

Monitoring by immunophenotypic techniques can also predict relapse. A specific
phenotype will be defined for each patient by sending a separate sample at diagnosis to the designated reference lab. It is expected that a suitable phenotype will be established for the majority of patients. Investigators will subsequently be asked to send a sample of bone marrow collected at the time of routine disease assessments to the reference labs for follow up monitoring. Laboratories for Immunophenotypic Characterisation and Monitoring:
Dr Sylvie Freeman Clinical Immunology Department of Immunology Division of Infection and Immunity Southmead Hospital University of Birmingham Westbury on Trym Tel: 0117 9596306 Birmingham, B15 2SZ Fax: 0117 959 6062 Tel: 01214158759 Mob: 07884310528 E-mail: [email protected] Fax: 01214143069 [email protected] Mr Steve Couzens Dr Christopher McNamara Department of Haematology Haematology Department University Hospital of Wales Royal Free Hospital Heath Park, Cardiff Tel: 02920742370 Fax : 02920745084 Tel: Tel: 0207 794 0500 e-mail: [email protected] Fax: 020 7830 2313 15.5 Assessment of the Clinical Value of Minimal Residual Disease Monitoring
Studies using molecular or immunophenotypic techniques have been shown in a
number of retrospective studies to be capable of predicting relapse. During the initial
phase of the AML17 trial the techniques established in the reference labs will go
through three phases of development. In phase 1, techniques to establish the predictive
relationship to relapse will be established for each technique/marker. In phase 2 this
predictive value will be prospectively validated within a new patient cohort to ensure that
it is valid in the context of the AML17 treatment schedules. During these phases the
reference labs will not be feeding back information to the investigators. This is explicit
in the Patient Consent Form 8. In phase 3, the aim is to establish clinically whether
having information that a patient has evidence of residual disease at very low levels is
Version 2: May 2008 clinically useful. This stage is anticipated to be underway at a later time point in the trial,
however work on the first two phases for some of the markers are already well
progressed.
When in itiated, the clinical value of monitoring will be assessed by randomising patients
shortly after diagnosis and before the response marrow is assessed, to be monitored or
not to be monitored. In these circumstances patients will be asked to consent to be
randomised to be monitored or not to be monitored. The monitored patients will be
required to agree to samples being taken according to the prescribed monitoring
schedule, which will be established for each marker in phases 1 and 2. If and when a
patient is found to have a significant level of MRD by any informative method (patients
may well be being monitored using more than one marker), the investigator will be given
this information, and will be asked to confirm that they have received this information.
The protocol leaves the question of therapeutic intervention to the discretion of the
investigator. They can, for example enter the treatment options provided for high risk
score patients.
It is recognised that repeated testing of this nature could cause patients extra anxiety,
but it could also provide reassurance. In order to assess this, the patient in this
randomisation will also be asked to participate in a Quality of Life assessment at 3, 6
and 12 months after the completion of chemotherapy
It is of the utmost importance that this assessment is carefully explained to patients and
consent should be obtained using Patient Information Sheet 8 and Consent Sheet 8
when this part of the trial opens.
16. MANAGEMENT OF PATIENTS WHO RELAPSE or are REFRACTORY
Patients who are entered into AML17 who are refractory (ie have not achieved complete remission after the second course of induction chemotherapy) or subsequently relapse will be eligible to be randomised to the high risk treatment options i.e. to receive either FLAG-Ida or Daunorubicin/Clofarabine, with a view to progressing to stem cell transplant. For patients with AML recurrence, it is becoming apparent that some "relapses" are genetically distinct from the features detected at original diagnosis and most likely represent therapy-related leukaemias following first-line therapy. This is a recognised cause of treatment failure in 2% of APL with chemotherapy-based regimens, although its frequency outside APL is unknown. Since this is clinically relevant, bone marrow or peripheral blood taken to diagnose relapse should also be sent for local cytogenetic analysis. In addition samples should be sent to one of the two reference laboratories for evaluation of molecular progression of the disease and to one of the reference immunophenotyping laboratories to assess stability of the immunophenotype. During the course of the trial newer molecularly targeted treatments are likely to become available and could be provided to patients who have entered the AML17 trial. Investigators will be informed of developments in this area by way of the regular newsletters and should discuss relevant cases with one of the Chief Investigators. 17. SUPPORTIVE CARE
The remission induction and consolidation phases of therapy are intensive and will be associated with a risk of infection and haemorrhage. The care of patients will make stringent demands on supportive care. Some information regarding aspects of supportive care will be Version 2: May 2008 collected in the patient record books, since this will be one factor to be taken into account in assessing the schedules. Participants should have local supportive care protocols. It is considered that policies related to the following aspects should be decided in advance to ensure that treatment-related complications are minimised. 1. Venous access via Hickman-type catheter 2. Control of nausea and vomiting 3. Mouth care 4. Prophylactic gut decontamination (if considered appropriate) 5. Antifungal prophylaxis 6. Response to a significant pyrexia — i.e. two readings of ≥38°C two hours apart, or a single reading ≥39°C 7. Antibiotic treatment of febrile episodes — including antibiotic choice(s) and monitoring, duration of therapy, and the treatment of non-response 8. G-CSF therapy [Lenograstim 263 µg (1 vial) s.c. daily in adults or 5 g/kg i.v. in children] may be given in case of prolonged neutropenia but it is not intended that it
should be part of routine supportive care
9. Irradiated blood products should be given to patients who receive Clofarabine or Fludarabine or Stem Cell Transplant. 18. CNS TREATMENT FOR ADULTS
The routine administration of treatment to the central nervous system is not recommended for patients with no evidence of CNS disease at diagnosis. Routine CNS investigation at diagnosis for patients without CNS symptoms is not recommended, but this should be considered for APL patients who relapse. Patients who present with CNS disease may be entered into the trial and be randomised at the same points as patients without obvious CNS involvement. If a patient presents with physical signs suggesting CNS disease, an intrathecal injection of Cytosine Arabinoside (50 mg) should be given when the diagnostic lumbar puncture is performed. If blast cells are identified in the CSF sample, a series of intrathecal injections with Cytosine Arabinoside should be given on 3 days each week until CSF samples are clear. This may need to be modified if the platelet count is very low or coagulation is abnormal. Thereafter, treatment should be repeated at intervals of approximately 2 weeks until consolidation treatment has been completed. Section D: ACUTE PROMYELOCYTIC
LEUKAEMIA
19. ACUTE PROMYELOCYTIC LEUKAEMIA
Version 2: May 2008 Patients will enter this part of the protocol at diagnosis with de novo or secondary acute promyelocytic leukaemia (APL) recognised morphologically as FAB-M3/M3v. Treatment with ATRA and supportive care for coagulopathy should be started as soon as the diagnosis is suspected, without awaiting results of cytogenetic/FISH/PCR analyses (see BCSH AML guideline (Appendix H). Diagnostic bone marrow (4mls in heparinised culture medium) and peripheral blood (30mls in EDTA) from all patients with suspected APL should be sent to Prof David Grimwade at Guy's Hospital (see Section 19.10 for address). Arrangements can be made for rapid confirmation of presence of PML-RARA fusion by PML immunofluorescence testing by contacting Prof David Grimwade (contact details, page ii), whose laboratory is also responsible for MRD testing. Confirmation of the molecular lesion is important because cases lacking the PML-RARA fusion will be under treated. Patients who enter the APL part of this trial will be monitored for minimal residual disease (MRD) (Section 15) with the aim of identifying patients failing first line therapy who require additional therapy in first CR (see Section 19.9) and will be assessed for Quality of Life and Health Economics impact. Patients entering this randomisation should use Patient Information Sheet 3 and
Consent Form 3

19.2 Objectives:

The primary objective of the trial is:

- To compare quality of life and toxicity and resource usage of patients receiving the
AIDA or the chemo-free treatment of ATRA + Arsenic Trioxide.

The secondary objectives are:
- To compare CR, OS and relapse rates in the two arms - To compare the kinetics of MRD in the two arms. 19.3 Entry Criteria:

Inclusion criteria:

- Signed written informed consent - Clinical diagnosis of APL and subsequently confirmed to have PML-RARA fusion - Age > 15 years - WHO performance status 0-2 - Serum total bilirubin < 2.0 mg/dL (≤51 umol/L) - Serum creatinine < 3.0 mg/dL (< 260 µmol/L) - Women of child-bearing potential (ie women who are pre-menopausal or not surgically sterile) must use acceptable contraceptive methods (abstinence. Intrauterine device (IUD) and must have a negative pregnancy test within 2 weeks of trial entry. Pregnant or nursing patients are excluded. Sexually active men must also use acceptable contraceptive methods Version 2: May 2008
Exclusion criteria:
- Age < 16 - Active malignancy at time of study entry - Lack of subsequent diagnostic confirmation of PML-RARA fusion at molecular - Significant arrhythmias, ECG abnormalities or neuropathy - Cardiac contraindications for intensive chemotherapy (L-VEF <50%) - Uncontrolled, life-threatening infections. - Severe uncontrolled pulmonary or cardiac disease. - Pregnant or lactating. 19.4 Arm A. - AIDA Treatment
19.4.1 INDUCTION
All-transretinoic acid, 45 mg/m²/day will be administered orally in two
equally divided doses and rounded to the nearest 10 mg increment,
starting on day 1. ATRA treatment will be continued until haematologic CR
and for a maximum of 60 days. Idarubicin, 12 mg/m² on days 2, 4, 6 and
8 by short (20 minute) intravenous infusion. Idarubicin doses should be
brought forward by one day in patients presenting with WBC>10, with first
dose given within a few hours of starting ATRA. If marrow appearances
are equivocal at around d30, then ATRA is continued. If haematological
CR is not achieved by 60 days after the start of induction the patient will
go off-study (and would be eligible for "High risk" APL protocols, see
Section 19.9).
19.4.2 CONSOLIDATION THERAPY
After the achievement of haematological CR, patients will receive three successive courses of consolidation chemotherapy and ATRA. Each course will be initiated at haematological recovery from the previous course defined as: ANC >1.5x109/L and platelets >100x109/L. In case of toxicity requiring a delay of more than 3 months from the initiation of the previous course, consolidation treatment will be discontinued and management discussed with a trial coordinator. First consolidation cycle
Idarubicin, 5 mg/m2/d by short (20 minute) intravenous infusion on days 1, 2, 3, 4.
ATRA, 45 mg/m2/d, will be administered orally in two equally divided doses and
rounded to the nearest 10 mg increment, given from day 1 to day 15.
Second consolidation cycle
Version 2: May 2008 Mitoxantrone, 10 mg/m2/d as 30 minute intravenous infusion on days 1, 2, 3, 4,
and 5.
ATRA, 45 mg/m2/d will be administered orally in two equally divided doses and
rounded to the nearest 10 mg increment, given from day 1 to day 15.
Third consolidation cycle
Idarubicin, 12 mg/m2/d as short (20 minute) intravenous infusion only on day 1.
ATRA, 45 mg/m2/d will be administered orally in two equally divided doses and
rounded to the nearest 10 mg increment, given from day 1 to day 15.
Marrow samples will be collected around day 60 (i.e. following course 1 in patients requiring prolonged ATRA to achieve CR, or following course 2 in those with earlier documentation of CR) and on regeneration following each consolidation course for testing by real-time quantitative PCR (RQ-PCR) by the reference laboratory for assessment of molecular remission. Patients who do not achieve molecular remission by the end of the 3rd consolidation cycle will be considered as molecular resistant and will go off study (eligible for protocols in Section 19.9). Marrow samples collected at earlier time points are used to measure disease response and provide early indication of patients at risk of failing first line therapy. 19.5 ARM B: ATRA with Arsenic Trioxide
19.5.1 INDUCTION
All-transretinoic acid (ATRA), 45 mg/m²/day will be administered orally
in two equally divided doses and rounded to the nearest 10 mg increment,
starting on day 1. ATRA treatment will be continued until haematological
complete remission (CR, see below for definition) or for a maximum of 60
days.
Arsenic Trioxide (As2O3=ATO), 0.30 mg/kg IV over 2 hours daily for 5
days (days 1-5) in week 1, and thereafter 0.25mg/kg IV over 2 hours twice
a week for an additional seven weeks.
If haematologic CR is not achieved by 60 days after start of induction, patient will go off-study. 19.5.2 CONSOLIDATION
ATRA, 45 mg/m²/day will be administered orally in two equally divided
doses and rounded to the nearest 10 mg increment. Treatment will be
administered for 2 weeks on followed by 2 weeks off, for a total of 7 cycles
(last cycle administered on weeks 25 - 26).
Version 2: May 2008 ATO, 0.30 mg/kg IV over 2 hours daily for 5 days, in week 1. In weeks two
to four ATO will be given on 2 days a week in a dose of 0.25mg/kg. This is
followed by four weeks with no treatment. This will be repeated for a total
of 4 cycles (last cycle administered on weeks 25 - 28).
Marrow samples will be collected at day 60 and after the end of consolidation cycles of ATO, to be tested by RQ-PCR for assessment of molecular remission (see below for definition). Patients who do not achieve molecular remission by the end of the 3rd consolidation cycle will be considered as molecular resistant and will go off study. Marrow samples collected at earlier time points are used to measure disease response and provide early indication of patients at risk of failing first line therapy. 19.5.2 Patients with High White Counts at Diagnosis
Patients who present with a peripheral white cell count of >10x109/l have a higher chance of developing differentiation syndrome if allocated to the ATRA plus Arsenic treatment. These patients should receive Mylotarg 6mg/m2 together with at least two doses of Rasburicase on day 1 of treatment. A second dose should be considered on day 4 if the white count has not fallen below 10x 109/l. These patients require close clinical and biochemical monitoring for evidence of differentiation syndrome and/or tumour lysis syndrome. 19.6 Quality of Life Assessments
All patients in the APL component of the trial will have a Quality of Life
assessment at baseline and 3, 6, 12, and 24 months from diagnosis. This
will take the form of the EORTC QLQC-30 questionnaire plus the Leukaemia
Specific Module which has been used in previous MRC AML trials, and the
Hospital Anxiety and Depression Scale (HADS). This will be sent to the
investigator at the appropriate times, who should arrange for the patient to
receive it. The patient will complete the questionnaire and return it (Freepost)
to the Trials Office.
19.7 Health Economics Assessment
Information will be collected on all patients as surrogates for resource usage. This will include time to neutrophil and platelet recovery, days in hospital, blood product usage, and days on antibiotics. This will be collected by the data collection system (internet or record books). In addition selected patients may be asked to complete a patient diary concerning medical events. For patients who are selected the diary will be sent to the investigator. 19.8 Treatment Modification
Version 2: May 2008 During induction treatment, ATRA may be temporarily discontinued in the presence of one of the following complications: Differentiation syndrome, pseudotumour cerebri, hepatotoxicity. ATO may be temporarily discontinued in the presence of differentiation syndrome, QT prolongation on ECG or hepatotoxicity; the drug will need to be discontinued permanently in the event of cardiac arrhythmias or severe neurological toxicity. 19.8.1 Differentiation (ATRA) Syndrome

This is accurately defined by the presence of: unexplained fever, weight gain, respiratory distress, interstitial pulmonary infiltrates, and pleural or pericardial effusion, with or without hyperleukocytosis. No single sign or symptom itself may be considered diagnostic of the syndrome. However, at the earliest manifestations of suspected Differentiation Syndrome (e.g. unexplained respiratory distress), and prior to development of a fulminant syndrome, the following measures should be immediately undertaken: temporary discontinuation of ATRA and ATO treatment. prompt initiation of dexamethasone 10 mg i.v. 12-hourly until disappearance of symptoms and signs, and for a minimum of 3 days. frusemide when clinically required. In patients treated with ATRA+ATO for induction, it is anticipated that induction of hyperleucocytosis (WBC >10) associated with induction of differentiation may occur in a proportion of patients. This does not require any change in therapy, beyond careful vigilance for development of differentiation syndrome. 19.8.2 Pseudotumour Cerebri
This is defined as presence of: severe headaches with nausea, vomiting, and visual disorders. In this case, generally developing in patients under 20 years of age, it is often necessary to discontinue ATRA treatment temporarily and to administer opiates. 19.8.3 Hepatotoxicity

This is defined as: an increase in serum bilirubin, AST/ALT, or alkaline phosphatase >5 times the normal upper level. This requires a temporary suspension of the ATRA. If hepatoxicity persists following discontinuation of ATRA, ATO should be temporarily discontinued in patients assigned to ATRA+ATO. The Idarubicin doses should not be changed on the AIDA arm. As soon as the symptoms and the patient's clinical condition improves, treatment with ATRA will be resumed at 50% of the previous dose during the first 4 days after the disappearance of retinoic acid syndrome, amelioration of pseudotumour cerebri or when serum bilirubin, AST/ALT or alkaline phosphatase are reduced to <4 times the normal upper level. Thereafter, in absence of worsening of the previous toxicity, ATRA should be resumed at full dosage. Version 2: May 2008 In case of reappearance of signs and symptoms of ATRA toxicity, the drug must be discontinued indefinitely during induction therapy. 19.9 Treatment of High Risk APL (relapse, molecular relapse, or
persistent MRD positivity)
Initial treatment of APL may fail, in which case patients will either relapse or be at high risk of relapse. In this study adult patients who relapse, or who are deemed to be at high risk of relapse based on molecular data, should be treated with Arsenic Trioxide or Gemtuzumab Ozogamicin (Mylotarg) and stem cell transplant options discussed with a trial co-ordinator. It is anticipated that during the course of the trial molecular criteria will become more precise as a result of the monitoring data (Section 19.10). As this evidence emerges investigators will be informed of patients who are considered high risk and who should be offered further treatment.
Note: At relapse, CNS should be checked for occult disease.
19.10 Molecular Diagnosis and Monitoring
Minimal residual disease monitoring is well established in APL and is an integral part of the treatment of patients in the AML17 trial. This is particularly important since overall the treatment strategy aims at a de-intensification of treatment, with omission of maintenance from the original AIDA schedule and removal of chemotherapy from the ATO+ATRA arm. Patients should be advised, as is stated in the information and consent form that this is the case and it will involve marrow samples (2-3mls first pull into EDTA) being taken after each consolidation course and then at 3-monthly intervals for 36 months, and that for technical or confirmatory reasons extra tests may be recommended. Samples should be sent to Professor David Grimwade at the address
below. Medical supervision of molecular diagnostics and MRD monitoring
and advice will be undertaken by Professor David Grimwade:
Molecular Oncology Diagnostics Unit, Clinical Laboratory Services Great Maze Pond, Tel: 0207 188 3699 Fax: 0207 188 2585 Mobile: 0780 329 3372 Email: [email protected] Version 2: May 2008 19.11 Supportive Care for APL Patients
APL treatment has some particular requirements with respect to supportive care which
are described in the BCSH Guideline (www.bschguidelines.com) an extract of which
is shown in Appendix G.
Version 2: May 2008 Section E: STATISTICS & TRIAL
GOVERNANCE
20. STATISTICAL CONSIDERATIONS
20.1 Patient numbers
Over the last 40 years, 5-year survival of younger patients in MRC AML trials has gone from 0% in AML4 to about 45% in AML12 and AML15. This dramatic improvement, which has changed AML from an invariably fatal disease into a potentially curable one, has been achieved not by any single major advance but through a series of small, but nonetheless important, increases in survival over a number of trials. However, there is great heterogeneity of outcome between different types of patient, and this is reflected in the design of the AML17 trial. There are approximately 700 cases of AML diagnosed each year in patients under the age of 60 in the British Isles, of whom about 15% have the APL sub-type. It is hoped that the majority of suitable patients will be entered into the trial. Indeed, recruitment to AML15 has typically run at around 650 patients per annum, so that over the course of the recruitment period it should be possible to randomise at least 300 APL patients and 2700 non-APL patients. For the APL randomisation, it is anticipated that a similar number of patients will be recruited from both the UK and GIMEMA and East German networks, giving a total of 600 patients for analysis. Outcomes are typically very good for this group of patients. It is anticipated that survival will be similar for these two treatment arms, however with 600 patients there will be over 80% power to establish equivalence based on a 7.5% difference in survival. However survival will remain a secondary objective in this part of the trial. Instead, the study will, as in AML15, use quality of life and resource usage as primary endpoints. With 600 patients it is possible to detect, with 80% power at p<0.05, a small-to-moderate difference of 0.25 standard deviations, and would have 90% power to detect a standardised difference of 0.27. Interim data from AML15 indicate that the standard deviation of the EORTC-QLQ30 global score is approximately 20 points, indicating that the trial will be powered to detect a 5 to 6 point difference in quality of life. The use of repeated measures modelling for the quality of life outcomes should increase the power to detect smaller differences. With 2700 patients entering the non-APL induction randomisation, there are likely to be some who will not be eligible for the 5-way randomisation, because of liver function tests. However, it is expected that approximately 85% of patients will be eligible to enter the five way randomisation. This means that the randomisation can recruit a maximum of 2300 patients over the course of the entire trial. This would mean a total of 1800 patients will contribute to a comparison of ADE v ADE + GO 3mg v DA +GO 3mg. This will give 80% power to detect a 10% difference in overall survival at 5 years between the two experimental arms and ADE, allowing for multiple testing by setting significance at p=0.025. These results will be meta-analysed with the accumulating data from AML15, where the same randomisation (ADE vs ADE+GO vs DA+GO) took place. Any analysis of the mylotarg dose question will depend on the results of any investigation of the interactions between chemotherapy regimen and mylotarg (whether the effect of Version 2: May 2008 mylotarg differs between ADE and DA chemotherapy). Assuming no interaction, the mylotarg dose question will have recruited some 1800 patients, giving 90% power to detect improvements in 5-year survival from 45% to 52.5% between the two Mylotarg doses. Interaction will be tested here using standard techniques. For the randomisations to targeted therapy, approximately 90% of patients (i.e. 2450 patients) will commence their second course of treatment. Data from previous MRC AML trials have been used to determine the likely recruitment to each question. It is anticipated that from current recruitment rates at least 400 patients will enter the CEP-701 randomisation where two thirds of the patients will receive CEP-701. Together with the approximately 100 patients who will be randomised (in a 1:1 fashion) as part of AML15, this gives a total of at least 500 patients in this comparison. Data from the AML10,12 trials show that five-year survival in this group is about 33%; so the meta-analysis of AML15 and AML17 should have 80% power to detect a difference in survival of 12% (from 33% to 45%). Just under 30% of patients starting their second course will be poor risk (i.e. approximately 700 patients). In the first instance, patients will be randomised between DClo v FLAG-Ida in a 2:1 randomisation. In the first half of the trial, therefore, one might expect a recruitment of around 300 patients. Five-year survival of this group of patients is currently 30%, so recruiting 315 patients in the first half of the trial will give 80% power to detect a clinically meaningful 15% improvement in survival from 30% to 45%. It is likely that other new therapies suitable for this group of patients will become available during the course of the trial and these can then be introduced by protocol modification. At present only around 40% of poor risk patients entering CR receive a transplant; with 360 patents randomised there will be approximately 80% power to detect an improvement from 40% to 55% in the numbers being transplanted. Assuming that around 15% of non-APL patients will have a core binding factor leukaemia, there remains a group of approximately 900 patients who do not fall into one of the predefined categories (CBF, FLT-3 positive, poor risk), and are therefore eligible for randomisation between mTOR inhibition and not. Assuming a 70% uptake of this randomisation, this means that there should be in excess of 600 patients who will be randomised in a 2:1 ratio.between mTOR inhibitor and not. With 600 patients recruited there will be 85% power to detect a 12.5% improvement in overall survival (from 50% to 62.5% at 5 years). Of the patients who are not considered to be "poor risk", at least 80% should enter CR and therefore eligible for the consolidation randomisations. This equates to around 1600 patients. Even if only two-thirds of such patients are randomised to the consolidation questions (roughly equivalent to the rate in AML15), there will be at least 1000 patients for the 3v4 randomisation. This will be powered as a non-inferiority trial with a one-sided significance level of p=0.025. With 90% power there will be sufficient power to detect or rule out inferiority in 5 year survival from CR of 65% versus 55%. To investigate the effect of MRD monitoring, the project will run in several stages. Initially, the best cut-offs will be identified; because a number of different time-points will be investigated, all analyses will be performed at a 1% significance level. Around 80% of patients enter CR, and it is anticipated that about 50% of these will achieve MRD negativity. Approximately half of all patients will relapse in the first 3 years. With a total of 360 patients entering CR (i.e. 450 patients with suitable markers), there will be 90% power to detect a difference between groups of 20% (40% versus 60% relapsing). Thus, it is planned that the first stage of the process will run for the first 600 patients, to allow for 20% of patients not having suitable markers. At this point the future direction Version 2: May 2008 of the MRD project will be assessed based on the preliminary results, and the treatment randomisation powered in line with the results found in the first stage. 20.2 Data analysis

Interim analyses of the main endpoints will be supplied periodically, in strict confidence, to
the MRC Leukaemia Data Monitoring and Ethics Committee (DMEC). In the light of these
interim analyses, the DMEC will advise the chairman of the Trial Steering Committee and
Chief Investigator if, in their view, one or more of the randomised comparisons in the trial
have provided proof beyond reasonable doubt* that for all, or for some, types of patient
one treatment is clearly indicated or clearly contraindicated.
The main analyses will be performed using standard contingency table and log-rank
methods based on the intention to treat — i.e. all patients believed to be eligible at the time
of randomisation will be included in the analysis, irrespective of protocol compliance, early
death, etc. The randomisations — and subsidiary data analyses — will be stratified by age
(0-14, 15-29, 30-39, 40-49, 50-59, 60+), performance status, and type of disease (de
novo/secondary AML). Consolidation randomisations will also be stratified by initial
allocation and by risk group, and comparisons of mylotarg dose will be stratified by
chemotherapy allocated. All analyses will assume that there may be some quantitative
differences in the size of any treatment effects in these different strata, but that there is
unlikely to be any qualitative difference (i.e. harm in one group, benefit in another).
21. TRIAL GOVERNANCE AND ADVERSE EVENT REPORTING
Cardiff University is the Trial Sponsor and has delegated certain responsibilities to participating sites. These define the responsibilities of the Principal Investigator on each site. The trial will be conducted in compliance with the MRC Guidelines for Good Clinical Practice in Clinical Trials copies of which are available from the MRC or the Trial Office. In the use of unlicensed drugs the trial is conducted under a CTA issued by the MHRA which requires the investigators to report Serious Adverse Events (SAEs) as described in below. The trial will be monitored by an independent Data Monitoring and Ethics Committee. 21.1 ADVERSE EVENT REPORTING
Principal Investigators at each participating institution have an obligation to report
relevant Serious Adverse Events (SAEs) which occur in this trial to the trial office in a
timely manner. It is recognised that adverse events which may be life-threatening are a
normal consequence of acute myeloid leukaemia or its effective treatment, and many
clinical changes in the patient's condition are expected.
21.1.1 Definitions:

For the purpose of this trial a Serious Adverse Event is defined as:
* Appropriate criteria of proof beyond reasonable doubt cannot be specified precisely, but a difference of at
least three standard deviations in an interim analysis of a major endpoint may be needed to justify halting, or
modifying, a randomisation prematurely. If this criterion were to be adopted, it would have the practical
advantage that the exact number of interim analyses would be of little importance, and so no precise
schedule is proposed.
Version 2: May 2008
• Development of a non-haematological toxicity of grade 3 as defined in the NCI Common Toxicity Criteria**, which does not resolve to grade 2 or less within 7 days • Development of any grade 4 non-haematological toxicity (excluding alopecia) • Development of neutropenia (<1.0 x 109/L) or thrombocytopenia (<50 x 109/L) for longer than 42 days after the end of chemotherapy in the absence of significant disease in the bone marrow (>5% blasts) • Any event which results in persistent or significant disability or incapacity • Any event which results in a congenital abnormality or birth defect • Death from any cause including persistent or progressive disease The following do not require to be reported as SAEs:
• Grade 4 haematological toxicity is an expected consequence of effective treatment, and is only required to be reported if it fulfils the criteria as defined above • Patients may present with some pre-existing toxicities which meet the criteria set out above, but it is only the development of these toxicities after entering the trial which should be reported • Neutropenic fever is an expected severe adverse event which may occur as a result of the disease or the treatment. This or its consequences do not have to be reported unless fulfilling the criteria set out above
21.1.2 Causality
Investigators will be asked to record their opinion as to whether the SAE as defined above was related to the study medication. This will be further reviewed by the Trial Management Group. 21.1.3 Collection of Data
Preliminary discussion of the event may take place with a clinical co-ordinator. SAEs should be recorded on the Adverse Event Form which is available on the trial website, and sent to the Trial Office in Cardiff. 21.1.4 Time of Report
Any death that is clearly not due to, or associated with, persistent or progressive
disease should be reported to the trial office within 24 hours.
21.1.5 Enhanced Pharmaco-Vigilance
For patients allocated to IMPs (Investigational Medicinal Products) there will be enhanced vigilance. This will involve a telephone enquiry from the Cardiff Trial Office weekly for up to 4 weeks after the administration of the IMP. The pharmaco-vigilance officer or her nominee will seek information of any treatment adverse effects or compliance difficulties. 21.1.6 Reporting to the Regulatory Authorities
The Chief Investigator or his nominee will review and record all SAEs. He will be responsible for reporting the events to the MHRA, COREC, and the Trial Steering Committee in the appropriate timelines. He will also report, where relevant, to the
** A copy of the NCI Common Toxicity Criteria is available from the Trial Office and on the website.

Version 2: May 2008 provider of the IMP (Investigational Medicinal Product) and produce periodic reports for all investigators to forward to the LREC. Version 2: May 2008 APPENDIX A: WHO Histological Classification of Acute Myeloid Leukaemias

Acute myeloid leukaemia with recurrent genetic abnormalities
Acute myeloid leukaemia with t(8;21)(q22;q22); (AML1(CBF )/ETO) Acute myeloid leukaemia with abnormal bone marrow eosinophils 9871/3 Inv(16)(p13q22) or t(16;16)(p13;q22); (CBFß/MYHII) Acute Promyelocytic leukaemia (AML with t(15;17)(q22;q12-21), (PML/RAR ) and variants. Acute myeloid leukaemia with 11q23 (MLL) abnormalities
Acute myeloid leukaemia with multilineage dysplasia

Acute myeloid leukaemia and myelodysplastic syndromes,
therapy-related

Acute myeloid leukaemia not otherwise categorised
Acute myeloid leukaemia minimally differentiated
Acute myeloid leukaemia without maturation Acute myeloid leukaemia with maturation Acute myelomonocytic leukaemia Acute monoblastic and monocytic leukaemia Acute erythroid leukaemias Acute megakaryoblastic leukaemia Acute basophilic leukaemia Acute panmyelosis with myelofibrosis Myeloid sarcoma
Acute leukaemia of ambiguous lineage
Undifferentiated acute leukaemia Bilineal acute leukaemia Biphenotypic acute leukaemia Version 2: May 2008 APPENDIX B: Preparation, Administration and Toxicity of Drugs used in AML17
Daunorubicin (CerubidinTM - May & Baker Ltd)
Daunorubicin is presented as a red powder in glass vials containing 20 mg with mannitol as a stabilising agent. The drug is reconstituted in sodium chloride 0.9% or water for injection. Following reconstitution, further dilution with sodium chloride 0.9% to a concentration of 1mg/ml is recommended. The resultant solution is given by a one hour infusion into a swiftly flowing drip. For hepatic dysfunction with a bilirubin 20-50 µmol/L reduce by 25%; for bilirubin >50 µmol/L reduce by 50%. In patients with renal impairment dose reduction should take place: Serum Creatinine 105-265µmol/L, reduce dose by 25%; Serum Creatinine >265µmol/L reduce dose by 50%. Side effects include nausea, alopecia, chronic and acute cardiac failure and dysrrhythmias. Subcutaneous extravasation may cause severe tissue necrosis.
Cytosine Arabinoside — Ara-C, Cytarabine (CytosarTM – Pharmacia & Upjohn)
Cytosar is available as a freeze dried powder containing 100 mg or 500 mg of Cytosine Arabinoside in a rubber capped vial. The diluent provided in the drug pack is water for injection containing 0.9% w/v benzyl-alcohol. Following reconstitution with the manufacturer's diluent the solution contains 20 mg/ml of Cytosine Arabinoside. At this concentration it is suitable for direct intravenous bolus injection into a central or peripheral line. Cytarabine solution is also available in a non-proprietary form from Pharmacia & Upjohn and Faulding DBL. These are presented as 20mg/ml and 100mg/ml solutions of cytarabine in a variety of vial sizes. It is recommended that before administration by intravenous bolus injection the hypertonic 100mg/ml solution is further diluted in water for injection, sodium chloride, 0.9%, or glucose, 5% solution, to produce a solution of 20mg/ml concentration. In patients with impaired hepatic function (bilirubin >34µmol/L) the dose should be reduced by 50%. No reductions are necessary for renal impairment. Side effects at the doses prescribed for remission induction include nausea, diarrhoea, oral ulceration and hepatic dysfunction. A Cytosine syndrome has also been described. It is characterised by fever, myalgia, bone pain, occasional chest pains, maculopapular rash, conjunctivitis and malaise. It usually occurs 6-12 hours following administration, and is more common with higher doses.
Etoposide (VP16-213) (VepesidTM - Bristol-Myers Pharmaceuticals)
Etoposide is available as a solution in ampoules containing 100 mg in 5 ml. The
appropriate dose should be diluted in sodium chloride 0.9% for infusion. The company
recommend that the infusion solution concentration does not exceed 0.25 mg/ml of
etoposide.

Give over at least 30 minutes as hypotension may be produced by excessively rapid
infusion.

For hepatic dysfunction with bilirubin of 26-51µmol/L reduce dose by 50%. At higher
bilirubin levels the decision to administer is a clinical one. For renal dysfunction dose
reduction should be: Creatinine Clearance (Cr Cl) of 60ml/min the dose should be 85%;
Cr Cl of 45ml/min reduce dose by 20%; for a Cr Cl of 30ml/min reduce dose by 25%.
Version 2: May 2008 Side effects include tissue necrosis if extravasation should occur, nausea, mucositis and alopecia. Anaphylactic-like reactions have been reported rarely and have responded to stopping the infusion and the administration of an antihistamine and hydrocortisone.
Gemtuzumab Ozogamicin — MylotargTM Wyeth Research

MYLOTARG (gemtuzumab ozogamicin for Injection) is supplied as an amber glass vial
containing 5mg of MYLOTARG lyophilised powder. This vial should be refrigerated (2-
8ºC).
Preparation
The drug product is light sensitive and must be protected from direct and indirect sunlight
and unshielded fluorescent light during the preparation and administration of the infusion.
All preparation should take place in a biologic safety hood with the fluorescent light
off. Reconstitute the contents of each vial with 5ml Water for Injection. Gently swirl each
vial. Each vial should be inspected to ensure dissolution and for particulates. (The final
concentration of drug in the vial is 1mg/ml). This solution may be stored refrigerated (2-8°
C) and protected from light for up to 8 hours. (Reconstituted vials of drug should not be
frozen.)
Before administration, withdraw the desired volume from each vial and inject into a 100ml
IV bag of 0.9% Sodium Chloride Injection. Place the 100ml IV bag into an UV protectant
bag. The following time intervals for reconstitution, dilution, and administration should be
followed for storage of the reconstituted solution: reconstitution ≤ 2 hours; dilution ≤ 16
hours at room temperature: administration; 2 hour infusion; i.e. a total of a maximum of 20
hours.
Administration
DO NOT ADMINISTER AS AN INTRAVENOUS PUSH OR BOLUS
Once the reconstituted MylotargTM is diluted in 100ml sodium chloride 0.9% for infusion, the
resulting solution should be infused over 2 hours. Prior to infusion inspect visually for
particulate matter and discoloration.

A separate IV line equipped with a low protein-binding 1.2-micron terminal filter must
be used for administration of the drug (see note). MYLOTARG may be given
peripherally or through a central line.
Premedication, consisting of an antihistamine (such as chlorpheniramine), should be given
before each infusion to reduce the incidence of a post-infusion symptom complex.
Methylprednisolone 50mg may also be used. Vital signs should be monitored during
infusion and for four hours following infusion.
Instructions for Use, Handling and for Disposal
Procedures for handling and disposal of cytotoxic drugs should be applied.

Cautions
Hepatic Insufficiency: Patients with hepatic impairment will not be included in the clinical
studies if the abnormality is greater than twice the local normal range.
Version 2: May 2008 Renal Insufficiency: Patients with renal impairment will not be included in the clinical
studies.

Note
The recommended in-line filter for Mylotarg administration is a 1.2-micron polyether sulfone
(PES) filter, e.g. "intrapurlipid" (Braun product number 4099702). If that filter is not
available, the following filters may be used: 0.22 micron PES, 0.20 micron cellulose
acetate, 0.8 to 1.2 micron cellulose acetate/cellulose nitrate (mixed ester), or 1.2 micron
acrylic copolymer.
Adverse Events
The most important serious adverse event may be hepatotoxicity or myelosuppression.
These should be reported to the Chief Investigator as described in Section 21. Other events
which have been reported in at least 10% of recipients of single agent Mylotarg include fever,
nausea, chills, vomiting, headache, dyspnoea, hypotension, and hyperglycaemia. It is not
necessary to report these events.
Fludarabine (FludaraTM - Schering-Plough)
Fludara contains 50mg fludarabine phosphate per vial. It should be given by slow intravenous infusion after dilution in 2ml water for injection. For hepatic dysfunction no dose change is required. For renal impairment a Cr Cl of 30 – 70 ml/min requires a dose reduction of 50%; greater impairment excludes the administration. The most frequent adverse event is myelosuppression. Patients less commonly suffer nausea, vomiting or alopecia. Fludarabine is a prolonged inhibitor of T-cells and has been associated with the development of transfusional GVHD and pneumocystis pneumonia. Rarely fludarabine has caused CNS side-effects with agitation, confusion and visual disturbance. Idarubicin (ZavedosTM - Pharmacia)
Idarubicin is available as a sterile pyrogen-free, orange-red freeze-dried powder, in vials containing 5 or 10 mg of idarubicin hydrochloride with 50 or 100 mg of lactose respectively. For administration the vial contents should be dissolved in water for injection to give a solution of 1mg/ml. The resultant solution should be administered intravenously into the side arm of a freely running intravenous infusion of 0.9% sodium chloride over 5 to 10 minutes. In children Idarubicin should be given as a 1 hour infusion. In cases with hepatic dysfunction dose reduction is required: bilirubin 21 – 34umol/L reduce the dose by 50%.Greater rises contraindicate the administration. For renal impairment with a serum creatinine 100 – 175umol/L reduce the dose to 50%.Administration at higher creatinine levels is a clinical decision. Side-effects: The major side effect is myelosuppression. Cardiac toxicity may occur, manifested by cardiac failure, arrhythmias or cardiomyopathies, either during therapy or several weeks later. The cumulative dose associated with cardiotoxicity is not own,but it is believed that a total dose of 60-80 mg/m2, which is considerably higher than that used in AML15, is not problematic. Idarubicin may cause a red discoloration of the urine for 1-2 days after administration. Reversible alopecia will occur, and some nausea or vomiting and oral mucositis should be expected. Elevation of liver enzymes and bilirubin may occur in a minority of patients. Idarubicin should not be given to patients with severe renal or liver impairment Version 2: May 2008 G-CSF- Human Granulocyte Colony-Stimulating Factor: (GranocyteTM -rHuG-CSF,
lenograstim - Chugai Pharma UK Limited) Granocyte is available as lyophilised power, each single use vial containing either 105µg of lenograstim (13.4 MIU rHuG-CSF) or 263µg of lenograstim (33.6 MIU rHuG-CSF). A pre-filled syringe of Water for Injections (1 ml) for each vial of Granocyte is provided for reconstitution before administration. Granocyte can now be stored at room temperature, up to 30°C. Dose in adults: In autologous PBPC mobilisation: 1 vial/day sc or as per local protocol In allogeneic PBPC mobilisation: 10 µg/kg/day for 4-6 days 1 vial/day sc or as per local protocol Chemotherapy induced neutropenia: 1 vial/day sc days 1-7 In FLAG regimen: 1 vial/day sc days 1-7 Dose in children: 5µg/kg up to a maximum of 1 vial (263µg) should be administered intravenously over 1 hour. Bone pain and injection site reaction have been associated with Granocyte treatment in some patients. Granocyte is distributed by Aventis UK, telephone 0870 5133347, Fax: 08705133329 Amsacrine (AmsidineTM - Parke Davis Co.)
Amsacrine is presented as two sterile liquids which are combined immediately prior to
use. The drug ampoule contains 1.5 ml of amsacrine, a bright orange-red liquid at a
concentration of 50 mg/ml. The diluent vial contains 13.5 ml of 0.0353 M L-lactic acid.
When 1.5 ml (75mg) of concentrated amsacrine is added to 13.5 ml of lactic acid diluent
the resulting solution contains 5 mg/ml of amsacrine (i.e. 75mg in 15ml).
It is recommended that preparation of the drug should be carried out using a GLASS
SYRINGE due to possible extraction of components of rubber or certain plastic material.
The solution should be added to 500 ml of 5% dextrose (in adults) and infused over a
period of 60 – 90 minutes. Amsacrine is incompatible with sodium chloride 0.9%.
In patients with impaired hepatic function (bilirubin > 34µmol/L) the dose should be
reduced to 60%. If renal function is reduced (Cr Cl < 60ml/min) the dose should be
reduced by 25%.
Side-effects: Some nausea and mucositis occur fairly frequently. Cardiac toxicity has
been described as with anthracyclines; the risk of arrhythmias is increased by
hypokalaemia. Hepatotoxicity is uncommon but is associated with a rise in serum
bilirubin and alkaline phosphatase. Phlebitis may be a problem with peripheral venous
access points and local necrosis is described. The risk of phlebitis can be decreased by
a slow rate of infusion. The degree of alopecia is variable but sometimes severe.
Mitoxantrone (NovantroneTM - Lederle laboratories)
Mitoxantrone is presented as a dark blue aqueous solution in vials of 20 mg, 25 mg and 30 mg (2 mg/ml) with saline and a buffer of sodium acetate and acetic acid. The required dose should be diluted to at least 50ml in 0.9% saline or 5% dextrose. It should be injected slowly (over >5 minutes) into a fast flowing infusion of 5% dextrose or 0.9% saline. (Alternatively the solution can be diluted in at least 50ml and given by short Version 2: May 2008 intravenous infusion). In hepatic dysfunction with a bilirubin > 60µmol/L maximum dose should be 8mg/m2. Side effects include tissue necrosis following extravasation outside a vein. It is probably slightly less cardiotoxic than daunorubicin but care should be taken to avoid low serum potassium levels. Anorexia, diarrhoea, stomatitis, fatigue and mild alopecia have also been described. Cyclophosphamide (EndoxanaTM – ASTA Medica)
Endoxana is available as a powder in vials containing 100 mg, 200 mg, 500 mg or 1000 mg of anhydrous cyclophosphamide and sufficient sodium chloride to render the reconstituted solution isotonic. The vial should be reconstituted with a suitable volume of Water for Injection to produce a 20mg/ml solution. This solution can then be administered by slow intravenous bolus injection or further diluted for infusion. The dose should be reduced in renal impairment: for GFR 10-50ml/min reduce dose by 25%; for GFR <10 the dose should be reduced by 50%. Side-effects: Haemorrhagic cystitis, mucositis, nausea and vomiting, and hypoglycaemia and hyperglycaemia may occur. ATRA (VesanoidTM - Roche Products)
The most common adverse effect of ATRA has been headaches of mild to moderate severity. Younger (paediatric) patients appear to be more sensitive to this particular effect. Bone pain, occasionally requiring analgesic treatment, has also been observed. Biochemical abnormality of liver function has occasionally been reported, specifically raised transaminases, alkaline phosphatase and bilirubin, but these are reversible on stopping the drug. The most serious adverse event has been a syndrome characterised by fever, respiratory distress and episodic hypotension, usually in association with leucocytosis (now known as "Differentiation Syndrome"). The onset of this syndrome has usually been in the first 1-2 weeks of drug treatment. Should this occur the ATRA should be stopped and steroids commenced as detailed in section 19.8.1 above. Some cases are reported to respond well to high-dose corticosteroid therapy (dexamethasone 10 mg i.v. 12 hourly for 3 or more days). Prolonged ATRA treatment may cause dryness of the skin. ATRA is also believed to be highly teratogenic and advice regarding contraception should be given as appropriate. Clofarabine (EvoltraTM Genzyme Inc)
Clofarabine is formulated at a concentration of 1mg/ml in sodium chloride (9mg/ml), (USP), and water for injection, USP, qs to 1 ml. Clofarabine is supplied in 2 vial sizes: a 1ml glass vial and 20 ml glass vial. The 10ml glass vials contain 5ml (5mg) of solution and the 20ml glass vials contain 20ml (20mg) of solution. For both vial types the pH range of the solution is 4.0 to 7.0. The solution is clear with colour ranging from colourless to yellow and is free from visible particulate matter. Dose, Administration and Storage: Vials containing undiluted Clofarabine for injection should be stored at controlled room temperature (15 to 30°C). Shelf-life studies of intact vials are currently ongoing. Clofarabine for injection should be filtered through a sterile 0.2µm syringe filter and then further diluted with 5% dextrose injection USP or European Pharmacopoeia (EP) (D5W) Version 2: May 2008 or 0.9% sodium chloride injection USP or EP (normal saline [NS]) prior to IVI. The resulting admixture may be stored at room temperature, but must be used within 72 hours of preparation. Clofarabine will be administered IV over 60 minutes daily for 5 consecutive days and repeated every 28 to 42 days. If patients develop somnolence (with or without dystonia), the infusion time may be increased to 120 minutes. To prevent drug incompatibilities, no other medications should be administered through the same IV line. Patients should not receive Clofarabine until a normal serum creatinine has been confirmed for the day of dosing. Arsenic Trioxide (TrisenoxTM – Cephalon Inc.)
Trisenox is 1mg/ml concentrate for solution for infusion (arsenic trioxide). It is presented as a sterile, clear, aqueous solution in a single–use 10ml ampoule. ATO is a trivalent inorganic arsenical. The active substance is a white crystalline powder that is very poorly soluble in water. Trisenox must be diluted with 100-250 ml of glucose (5%) injection or sodium chloride 9mg/ml (0.9%) injection immediately after withdrawal from the ampoule and must not be mixed with or concomitantly administered in the same intravenous line with other medicinal products. Aseptic technique must be strictly observed throughout the handling of Trisenox since no preservation is present. After dilution in intravenous solutions, Trisenox is chemically and physically stable for 24 hours at 15-30o C and 48 hours at refrigerated temperatures (2-8ºC). From a microbiological point of view, the product must be used immediately. If not used immediately in-use storage times and conditions prior to use are the responsibility the user and would normally not be longer than 24 hours at 2-8ºC, unless dilution has taken place in controlled and validated aseptic conditions. Trisenox is given as a slow infusion over 1-2 hours daily until bone marrow remission is achieved. The daily infusions should be given on an inpatient basis at the beginning of induction therapy, followed, when the acute symptoms of APL have resolved and the patient's condition is stable, by outpatient administration for the remaining induction and consolidation treatment period. CEP-701 (Cephalon Inc.)
The study drug should be stored, under adequate security, in the pharmacy at the study centre at a controlled room temperature of 20ºC to 25ºC (68ºF to 77ºF), protected from light, until taken by the study patients or until returned to Cephalon or its designated agent. The study drug is stable for at least 30 months from the day of manufacture if stored in amber bottles, protected from light, at a controlled room temperature below 25ºC. Further information on CEP-701 is provided in Appendix C.
RAD001 (Everolimus Novartis)
RAD001 has been given as monotherapy to nearly 1000 patients with advanced cancer and over 100 healthy volunteers. Phase I studies established safety at 10mgs oral daily or 50mgs oral weekly. The most frequent side effects which occurred in 15% of patients was stomatitis and fatigue. Some patients also developed hyperglycaemia. Some Version 2: May 2008 patients developed a rash or erythema. Biomarker analysis indicated efficacy with both
daily weekly dosing schedules.
Human Pharmacokinetics and Metabolism
General Clinical Pharmacokinetics
Absorption
Following oral administration in patients with advanced solid tumours, RAD001 is rapidly
absorbed with a median time to peak concentration of 1-2 hours post dose. The steady-
state AUC0- is dose-proportional over the dose range of 5 to 70mg in the weekly
regimen and 5 to 10mg in the daily dosing regimen. Cmax is dose-proportional between
5 and 10mg for both the weekly and daily regimens. At doses of 20mg/week and
higher, the increase in Cmax is less than dose-proportional. The coefficient of variation
between patients is approximately 50%. Similar exposure-dose relationship was also
noted in kidney transplant patients in a single-dose escalation study. The extent of
RAD001 absorption in renal transplant patients (n=4), when RAD001 was administered
as a solid dispersion in capsule concomitantly with cyclosporine, was estimated to be
about 11% or higher based on the amount of radio-labelled RAD001 present in blood at
tmax.
RAD001 is a substrate and weak inhibitor of P-glycoprotein.
Food Effects
When RAD001 was administered as six 0.25-mg dispersible tablets in healthy subjects,
a high-fat breakfast reduced Cmax by 50% and delayed the median tmax by 2 hours.
However, the high-fat breakfast had no apparent effects on the AUC and t1/2. The
RAD001 blood concentrations in the post-absorption phase between 4 to 72 hours post-
dose were similar when RAD001 was administered with food or without food.
When RAD001 was administered as two 1-mg Certican MF tablets in healthy subjects,
a high-fat breakfast reduced Cmax by 60% and delayed the median tmax by 1.3h. There
was a 16% reduction in AUC. However, the RAD001 blood concentrations in the post-
absorption phase between 4 to 72 hours post-dose were similar when RAD001 was
administered with food or without food.
Thus, food can potentially reduce the Cmax/ Cmin ratio of RAD001 at steady-state in the
daily dosing regimen.
Distribution
The distribution of RAD001 between human blood cells and plasma was concentration-
dependent over the range of 5 to 5000ng/mL. The proportion of RAD001 confined to
plasma is approximately 20% at the concentration observed in cancer patients given
10mg/day of RAD001 whereas it increased from 17 to 73% over the wide concentration
range (5-5000ng/mL). Plasma protein binding is approximately 74% in healthy subjects
as well as patients with moderate hepatic impairment.
Version 2: May 2008 Metabolism
RAD001 is extensively metabolized in the liver. It is a substrate of CYP3A4. The main
metabolic pathways identified in humans were mono-hydroxylations and O-
dealkylations.
Two main metabolites were formed by hydrolysis of the cyclic lactone. The parent drug,
RAD001 was the main circulating component in blood. None of the main metabolites
contributes significantly to the pharmacological activity of RAD001.
Excretion
Elimination is essentially that of RAD001 metabolites in the bile. Elimination half-life in
cancer patients averaged 30 hours, which is similar to that in healthy subjects. After a
single dose of [14C]RAD001 in renal transplant patients, the majority (80%) of
radioactivity was recovered in the faeces, only a minor amount (5%) was excreted in the
urine over the 10-day collection period. Parent drug was not detected in urine and
faeces.


Elderly
A limited reduction in RAD001 oral clearance by 0.34% per year of age was estimated
in adults (age range studies were 16-70 years). No dose adjustment for elderly patients
is considered necessary.
Contraindications, possible risks and adverse events
RAD001 should not be administered to patients with a known hypersensitivity to
RAD001 (Everolimus) or other rapamycins (sirolimus, temsirolimus) or to its excipients.
Interactions with other medications
RAD001 is a substrate of CYP3A4, and a substrate and moderate inhibitor of P-
glycoprotein. Pharmacokinetic interaction with drugs which modify CYP3A4 enzymes
have been reported. Drugs in this category frequently used in oncology patients include
the azole antimycotics (itraconazole, ketoconazole) and erythromycin which are
CYP3A4-inhibitors and the anti-epileptic drugs phenytoin and Carbamazepine which are
CYP3A4 inducers.
Co-administration with strong CYP3A inhibitors (eg ketoconazole, itraconazole,
ritonavir), and strong inducers (eg rifampin, rifabutin) should be avoided.
Version 2: May 2008
Co-administration with moderate CYP3A inhibitors (eg erythromycin, fluconazole,
calcium channel blockers, benzodiazepines) and moderate inducers (eg
carbamazepine, Phenobarbital, phenytoin) should also be avoided if possible or used
subject to caution (eg increased frequency of safety monitoring, temporary interruption
of RAD001).
Co-administration with substrates, inducers, or inhibitors of P-glycoprotein should be
avoided if possible, or used subject to caution (eg increased frequency of safety
monitoring, temporary interruption of RAD001).
Grapefruit and grapefruit juice affect cytochrome P450 and –glycoprotein activity and
should therefore be avoided. Lists of clinically relevant inhibitors and inducers can be
found in the Investigator Brochure.
Special patient populations
Hepatic impairment
The oral clearance (CL/F) of RAD001 in patients with mild-moderate hepatic impairment
(Child-Pugh Class A or B) was approximately half of that in subjects with normal liver
function. For patients with their serum bilirubin >34 µmol/L (>2 mg/L), serum albumin
<35g/L (<3.5 g/dL), and INR > 1.3 (>4 second prolongation of prothrombin time), the
dose of RAD001 should be reduced to one-half of the dose for patients with normal liver
function. Patients with severe liver function impairment should not be entered into
clinical trials.
Renal impairment
Renal impairment has little or no impact on the pharmacokinetics of RAD001.
Elderly
No dose adjustment is required for advanced age.
Ethnicity
Pharmacokinetic characteristics are not notably different between Caucasian and
Japanese subjects whereas in Black transplant patients pharmacokinetic studies have
shown an average 20% higher clearance. In oncology studies, dose modification for
reason of ethnicity is not considered necessary given the apparent broad window for
dose effect in the Phase 1 pharmacodynamic studies.
Use in Pregnancy and lactation
RAD001 must not be administered to pregnant women or to women who are breast
feeding. Negativity of a recent pregnancy test is a required selection criterion for
women of child-bearing potential.
Version 2: May 2008 Effective contraception must be practiced by patients for the duration of studies.
Studies in animals have shown reproductive toxicity effects including
embryo/foetotoxicity. The potential risk for humans is unknown. Limited data are
available concerning exposure to RAD001 in pregnancy in transplantation patients. Out
of six women exposed to RAD001 immediately before and/or shortly after becoming
pregnant, 4 delivered healthy babies, 2 terminated their pregnancies voluntarily, one
had a spontaneous rupture of the membranes after 30 weeks gestation (the baby died 3
days after vaginal delivery). Two cases of paternal exposure were recorded, each
resulting in healthy babies. The information provided by these data are insufficient to
draw a meaningful conclusion on the effects of RAD001 exposure during pregnancy or
lactation. In oncology studies, conception should be prevented during treatment with
RAD001 and the drug must not be administered to pregnant women.
It is not known whether RAD001 is excreted in human milk. In animal studies, RAD001
and/or its metabolites were readily transferred into the milk of lactating rats. Therefore
women who are taking RAD001 should not breast feed.

Oral anticoagulants such as warfarin are CYP2C9 substrates and, as such, no
interaction with RAD001 is expected. However, drug-drug interaction studies between
macrolide antibiotics and warfarin have produced missed outcomes and the disparity in
these findings has led to the conclusion that multiple factors may alter the clearance of
warfarin. The Coadministration of RAD001 and oral anticoagulants is possible but
should be subject to verification of coagulation (INR) once steady state is reached (after
one week's treatment).
RAD001 and oral contraceptives
Preclinical and clinical data have shown RAD001 to have CYP3A4 inhibitory activity
rather than induction activity, induction or metabolism of contraceptive hormones by
RAD001 is unlikely. Consequently, administration of RAD001 should not reduce the
efficacy or oral contraceptives
Version 2: May 2008 APPENDIX C: Background Information on CEP-701

Name and Description of Investigational Product CEP-701 is an orally bioavailable receptor-tyrosine kinase inhibitor. The compound is a chemically synthesized derivative of K-252a, a fermentation product of Nonomurea longicatena, and belongs to a class identified as indolocarbazole alkaloids. CEP-701 drug product is supplied in a carrier of polysorbate 80 NF and propylene glycol USP, 25 mg CEP-701/ml, in 100ml glass bottles. A more detailed description of the treatment is provided in Section 11.3. Findings From Nonclinical and Clinical Studies
Nonclinical Pharmacology
CEP-701 exhibits most potency in the inhibition of the neurotrophin receptor Trk A (tropomyosin receptor kinase) (concentration at which 50% of the enzyme is inhibited [IC50] 3 nM) and the fms-like tyrosine kinase, FLT3 (IC50 3 nM). In addition, CEP-701 can be classed as a moderately potent inhibitor of vascular endothelial growth factor receptors (VEGFR) 1 to 3 (IC50 37 to76 nM), mixed lineage kinases 1 to 3 (IC50 11 to71 nM), and c-Jun N-terminal kinases 1β1 (IC50 81 nM), 2α2 (IC50 113 nM), and 3α1 (IC50 31 nM). It displays weaker inhibitory activity against platelet-derived growth factor receptor β (IC50 216 nM), rat brain protein kinase C (IC50 226 nM), and fibroblast growth factor receptor (IC50 420 nM). CEP-701 does not show appreciable inhibition of epithelial growth factor receptor or the β-insulin receptor kinase. When added to intact cells under plasma-free conditions, CEP-701 inhibits TrkA and FLT3 with IC50 of 25 and 1 to 2 nM, respectively. The inhibition of Trks by CEP-701 may be of value as therapy for both prostate cancer and paediatric neuroblastoma, where this family of tyrosine-receptor kinases is believed to play a role in tumour cell survival and/or invasive growth. Treatment of rats bearing the Dunning H rat prostate cancer with CEP-701 caused a significant regression of established tumours, (Cephalon data on file). CEP-701 was also shown to inhibit the growth of DU145, PC3, and CWR22Rv1 human androgen-independent prostate cancer xenografts in nude mice. Studies with human neuroblastoma cell lines have been performed with CEP-751, a close analog of CEP-701 that is metabolized to CEP-701 in vivo. Treatment of nude mice bearing such xenografts with CEP-751 resulted in a significant inhibition of tumour growth. Nonclinical Pharmacokinetics
Pharmacokinetic parameters for intravenous (iv) CEP-701 are similar in rats and dogs, with a plasma clearance of 0.8 l/hr⋅kg, a volume of distribution of approximately 1.4 l/kg, and an elimination half-life (t½) of 1.2 hours. Orally administered CEP-701 is rapidly absorbed in both rats and dogs, with peak plasma concentrations occurring within 2 to 4 hours of dosing. In dogs, the absolute oral bioavailability of CEP-701 from a vehicle composed of polysorbate 80 and propylene glycol is 39%. The oral bioavailability of CEP-701 from solution formulations in dogs is more than 10-fold higher than in rats. In vitro, CEP-701 binds with high affinity to human alpha-1-acid glycoprotein (hAGP), resulting in an estimated unbound, biologically active fraction of less than 1% in human plasma. The binding appears saturable. In an intact cell assay, hAGP (1 mg/ml) shifted Version 2: May 2008 the IC50 value of CEP-701 for TrkA 750-fold, from 8 nM to 6000 nM. In the same assay, 2 samples of human plasma caused 250- and 500-fold shifts in this IC50 value. The significance of these findings with respect to the clinical activity of CEP-701 is not known; however; they most probably explain the need to attain micromolar plasma concentrations of CEP-701 in order to observe biological effects in patients. CEP-701 is primarily metabolised via hydroxylation and glucuronidation. Results from an in vitro study with cDNA-expressed human cytochrome P450 enzymes (CYP) indicate that CYP3A4, CYP1A2, and CYP2B6 may be involved in the metabolism of CEP-701. CEP-701 inhibits several CYP isoforms in human liver microsomal preparations, with Ki values below 5 µM (approximately 2 µg/mL) for CYP1A2, CYP2C9, and CYP3A4; and 10 µM (approximately 4 µg/mL) for CYP2C19. The potential for CEP-701 to inhibit these CYP isoforms in vivo has not been assessed. Caution regarding concomitant administration of drugs that are substrates for these CYP isoforms, and especially those with narrow therapeutic indices, would be prudent. Nonclinical Toxicology
The toxicity of CEP-701 has been evaluated in single-dose oral administration studies in mice, rats, and dogs (table C1). In addition, repeated-dose oral administration studies have been completed in rats (6 months) and dogs (9 months). In the single-dose studies, the lethal dose at which 10% of mice died after experiencing adverse events (LD10) was 73 mg/kg, and an LD50 of 103 mg/kg was determined in rats. A maximum tolerated dose (MTD) of 100 mg/kg was determined in dogs. Table C1: Summary of Key Toxicology Parameters
Parameter
(mg/kg/day)
(mg/m2/day)
(mg/day)
a Extrapolated data, assuming a body surface area of 1.73 m2. LD10 = the dose at which 10% of the species experienced adverse events that resulted in death. LD50 = the dose at which 50% of the species experienced adverse events that resulted in death. MTD = maximum tolerated dose. In a 6-month study, rats received CEP-701 by oral gavage at 0.8, 4, or 20 mg/kg/day. There was no compound-related mortality. A reduction in body weight gain was observed in all dose groups relative to the deionised water control group, including the CEP-701 vehicle group. However, the most prominent reduction in body weight gain (9% to 11% relative to vehicle) was noted in the 20-mg/kg/day CEP-701 dose group. No CEP-701-related changes were noted in ophthalmology, haematology, serum chemistry, or urinalysis data. Changes interpreted to be related to administration of CEP-701 were detected microscopically in the epithelium of the anorectal junction, caecum, extrahepatic bile duct, and the main pancreatic duct. Microscopic changes were described as "epithelial cell alteration" (bile duct, pancreatic duct, and caecum) Version 2: May 2008 and inflammation (anorectal junction). Treatment-related changes in these epithelia were subtle, did not occur in all treated animals/sections of affected groups, and, in some sites, were morphologically similar to microscopic changes that occurred in some control animals. No treatment-related changes were found histologically in rats following a 6-week recovery period. On the basis of the results of this 6-month oral toxicity study, 20 mg/kg/day of CEP-701 was identified at the MTD in rats. In a 9-month study, dogs received CEP-701 by oral gavage at dosages of 0.2, 1, and 5 mg/kg/day. There was no compound-related mortality or morbidity. An increased incidence of emesis was noted in both male and female dogs in the 5.0 mg/kg/day dose group relative to dogs in both control groups. In general, increased salivation was noted in male and female dogs only in the 5.0 mg/kg dose group. There were no other compound- related clinical observations. There were no compound-related changes noted in body weights, food consumption, ophthalmology, haematology, serum chemistry, urinalysis, electrocardiograms, or organ weight data. Changes interpreted to be related to CEP-701 were detected microscopically in the mucosa of the anorectal junction of both male and female dogs in the 5.0 mg/kg/day dose group. Many dogs from the other groups, including the deionised water and vehicle control groups, also had evidence of inflammation within the anorectal mucosa. However, in the high-dose group, the inflammation was more severe and there was evidence of hyperplastic changes within deeper layers of the anorectal epithelium. In addition, the high-dose group had a shift in cell populations that included large numbers of neutrophils, especially in the squamous mucosa of the anal area. There were no new treatment-related histologic changes following the 9-week recovery period. Basal cell hyperplasia also resolved, indicating that the chronic irritation with CEP-701 administration had subsided. On the basis of the results of this 9-month oral toxicity study, 5 mg/kg/day of CEP-701 was identified as the MTD in dogs. In addition to these findings, it is noted that a dosage of 15 mg/kg/day in dogs was found to be associated with significant toxicity when administered for 28 days. Clinical signs included hunched posture, decreased activity, weight loss, vomiting, and increased salivation. Faecal occult blood was increased in these animals, and gastrointestinal haemorrhage was noted in some males. Four of the 10 dogs dosed at 15 mg/kg/day were euthanised in extremis prior to the completion of the 28-day study. Terminal serum chemistry findings in these animals were consistent with cholestasis, and hepatic inflammation and necrosis. Treatment-associated lesions were observed throughout the gastrointestinal tract as well as in the liver, gallbladder, bile duct, prostate, and thymus. The day-28 toxicokinetics revealed a maximum plasma concentration (Cmax) of 385 ng/ml in males and 606 ng/ml in females, and an area under the plasma concentration-time curve from time zero to 24 hours (AUC0-24) of 1365 and 733 ng⋅hr/ml, respectively. A battery of in vitro and in vivo tests for genotoxicity has been conducted with CEP-701. CEP-701 was negative in the bacterial point (Ames) assay and the in vivo aneuploidy/ micronucleus assay. CEP-701 was positive in the mouse lymphoma mutagenesis assay (–S9 5.0 µg/ml, +S9 2.5 µg/ml), and also caused increased percentages of polyploidy (–S9 ≥0.4 µg/ml) and endo-reduplicated cells (+S9 ≥5.0 µg/ml) in the Chinese hamster ovary cell chromosome aberration assay. In a chromosome aberration assay with human peripheral blood lymphocytes (HPBL), CEP-701 caused an increase in the number of polyploid cells (–S9 ≥0.38 µg/ml, +S9 ≥2.0 µg/ml). In a separate study with HPBLs, CEP-701 was able to induce Version 2: May 2008 micronuclei (–S9 0.74 µg/ml, +S9 1.4 µg/ml). Subsequent investigation into the mechanism of action via the application of a pain-centromeric DNA probe indicated that micronuclei were generated via an aneugenic mechanism. Ancillary pharmacology studies of CEP-701 suggest little potential for interaction with the cardiovascular and gastrointestinal smooth muscle systems. Effects on renal excretion and interactions with the central nervous system were apparent only at oral doses of 100 mg/kg or above. Clinical Experience
Healthy Subjects
The safety and pharmacokinetics of single doses of oral CEP-701 from 3 to 20 mg were evaluated in healthy subjects (study M97-792). Nine subjects were treated at each dose; 6 received active drug and 3 received a placebo. Cmax of CEP-701 ranged from 114 to 1041 ng/ml, mean AUC from 929 to 7889 ng⋅h/ml, and mean apparent t½ from 6.8 to 9.2 hours. There was no significant departure from dose proportionality. In the second stage of the study, in which 12 subjects received 10 mg CEP-701 under fasting and non-fasting conditions, the time to maximum plasma concentration (tmax) was lengthened from 1.8 hours to 3.7 hours (p<0.001) and Cmax reduced from 403 to 294 ng/mL (p=0.002) when CEP-701 was taken with food. CEP-701 was well tolerated and treatment-emergent adverse events were mild in nature (headache, sweating, constipation). No clinically significant abnormal haematology, chemistry, urinalysis, or stool laboratory values were observed. In a separate study (study M99-067), the tolerability of oral CEP-701 vehicle (polysorbate 80 and propylene glycol, USP) was assessed in 24 healthy subjects who were administered twice-daily volumes of 3.2 to 9.6 ml of the vehicle diluted to 30 ml in apple juice for 14 days. Results indicated that the vehicle alone was well tolerated at volumes used in clinical studies. Patients With Cancer
The safety and/or efficacy of CEP-701 in cancer patients has been explored in 5 Phase 1 or Phase 2 studies. In a pilot study, CEP-701 was administered preoperatively for 5 days at 40 mg bd to 9 men with localized prostate cancer who had elected to have radical prostatectomy (study M99-108). In 5 patients who completed the study, the mean plasma concentration of CEP-701 was 427.9 ng/ml immediately prior to surgery, and the mean prostate tissue concentration was 97.1 ng/g, indicating reasonable tissue penetration. The MTD and dose-limiting toxicities (DLTs) of repeated doses of CEP-701 were defined in a study of patients with advanced solid tumors (study M98-909). A total of 30 patients were enrolled at twice-daily doses of 5 mg (n=3), 10 mg (n=3), 20 mg (n=3), 40 mg (n=13), 80 mg (n=7), and 120 mg (n=1). The majority of patients (67%) received a single 28-day cycle of CEP-701. However, 7 patients received study drug for at least 3 months, including 3 patients who were treated for more than 6 months. One patient received 13 cycles of treatment. The most frequently reported adverse events were nausea (63%), diarrhoea (47%), anorexia (37%), asthenia (30%), constipation (27%), and vomiting (27%). The incidence of adverse events tended to be greater in patients who received at least 40 mg bd. Most of these events were intermittent, but lasted several days. Version 2: May 2008 Dose-limiting toxicities were reported for 1 patient at 80 mg bd (grade 3 nausea) and 1 patient at 120 mg bd (grade 3 hypotension). The formal definition of MTD was not met for either of these dosages, but treatment-related adverse events, especially of the gastrointestinal system, made CEP-701 poorly tolerated at 80 mg and above. After expanding the MTD group (40 mg bd) to 13 patients, DLTs were reported in 2 patients at this dosage (grade 3 anorexia, nausea, dyspepsia and grade 3 asthenia). Thus, the MTD of CEP-701 without antiemetic prophylaxis was considered to be 40 mg bd. However, in view of the intermittent nature of many of the gastrointestinal events, the tolerability of higher dosages (60 and 80 mg bd) is considered worthy of further study when CEP-701 is given with appropriate antiemetic support. The pharmacokinetics of CEP-701 in patients with cancer were found to be similar to those in healthy subjects. CEP-701 was rapidly absorbed, with mean tmax values ranging from 0.8 to 2.7 hours on days 1 and 28 across all dosages. At 40 mg bd, the day-28 mean Cmax was 3973 ng/mL, and the mean AUC0-12 was 26630 ng⋅hr/mL. At 80 mg bd, the day-28 mean Cmax was 12117 ng/mL, and the mean AUC0-12 was 114857 ng⋅hr/ml. Plots of dose-normalized CEP-701 AUC0-12 on days 1 and 28 indicated greater than dose-proportional increases in AUC0-12 after multiple doses. As a result there was greater accumulation of CEP-701 with bd administration at higher doses, with mean accumulation factors of 0.9 at 5 mg, 1.7 at 10 and 20 mg, 3.0 at 40 mg, and 4.1 at 80 mg. CEP-701 did not produce an objective tumour response in any patient. The median duration of treatment was 5 weeks. Three patients had stable disease for more than 6 months and 1 of the patients with small cell lung cancer was stable for almost a year. In study M99-051, a 40-mg bd dosage of CEP-701 was shown to be ineffective in maintaining or lowering prostate specific antigen concentrations in patients with hormone-refractory prostate cancer. Eight-week trough plasma concentrations of 1538 ng/ml (n=37) were similar to plasma concentrations observed in earlier studies. Nausea and diarrhoea were the most common adverse events, observed in 42% and 30% of patients, respectively. Severe gastrointestinal events (nausea, vomiting, abdominal pain, diarrhoea) considered possibly or probably related to CEP-701 were recorded for 7 of the 159 patients enrolled in the study. In addition, there were 4 reports of moderate to severe gastrointestinal hemorrhage, of which 1 event was considered possibly related and the other 3 unrelated to study drug. Preliminary findings are available from 2 recently completed studies. In the first study (study C0701a/102/ON/US), 19 patients with advanced pancreatic cancer received CEP-701 at 20 and 40 mg bd in combination with a standard regimen of gemcitabine. The study was closed early because of lack of efficacy. Preliminary assessment of safety data indicated that the combination of CEP-701 with gemcitabine did not result in significant additive toxicity. A single serious adverse event of acute renal failure was considered possibly related to CEP-701. The second study (study C0701a/202/ ON/US) explored the activity of CEP-701 in 18 patients with refractory or relapsed AML with activating mutations of the Version 2: May 2008 receptor tyrosine kinase FLT3. The starting dosage of CEP-701 was raised in this study from 40 mg bd to 60 mg bd after the first 4 patients showed no response and a cell-based exvivo assay of plasma indicated that the inhibition of the FLT3 target may have been suboptimal. Fourteen patients were subsequently enrolled at 60 mg bd, and the dosage for 3 patients was increased to 80 mg bd after approximately 1 month of treatment. The higher dosages of 60 and 80 mg bd appeared to be relatively well tolerated in this group of patients. At a dosage of 60 mg bd, ex vivo assay indicated that a high degree of inhibition (>90%) of the FLT3 target was maintained over the 12-hour interval between doses. Transient decreases in the number of peripheral blast counts and the recovery of elements of the normal peripheral cell population were documented in several patients. Serious adverse events of gastrointestinal haemorrhage, fatigue and congestive heart failure in 1 patient each were considered possibly related to CEP-701. These events were also considered possibly related to the patients' disease and/or prior treatment. Known and Potential Risks and Benefits to Human Subjects
The principal treatment-related side effects of CEP-701 are gastrointestinal in nature (nausea, diarrhoea, anorexia, constipation, and vomiting). Asthenia has also been reported. Severe events are relatively uncommon, and clinical experience suggests that the nausea and vomiting should respond to 5-HT3 receptor antagonist antiemetics. These effects are consistent with the gastrointestinal signs and symptoms observed in repeat-dose toxicology studies in animals. More severe findings of cholestasis and hepatic inflammation that were observed in the 28-day dog toxicology study have not been manifested in the clinical program to date. Gastrointestinal hemorrhage has been reported in a small number of patients. It is not known to what extent these hemorrhagic events are related to CEP-701 treatment. The benefits of CEP-701 to patients remain to be determined. Transient decreases in peripheral blast count have been observed in some patients with refractory AML treated with CEP-701. A scientific rationale, based on in vitro studies and animal cancer model data, exists to support the potential benefit of inhibiting FLT3 in patients with AML and of inhibiting Trks in patients with prostate cancer and neuroblastoma. Additional information regarding risks to human subjects may be found in the Investigator's Brochure. Version 2: May 2008 APPENDIX D: Instructions to the Patient/Caregiver for Administering CEP-701

General Instructions
1. Store at room temperature of 20 to 25°C (68–77°F). Protect from light. Keep used
and unused vials in original vial box. Keep Out of Reach of Children. For Oral Administration Only. 2. Return all used and unused vials in original vial box at each study visit. 3. CEP-701 may be taken with food. If you vomit after a dose, do not repeat this dose. You should take your next dose at the regular scheduled time. 4. Administer this study drug in the morning and in the evening, approximately every 12 hours (there must be at least 8 hours between doses). 5. See your physician or pharmacist if you have any questions.
Dosing of CEP-701 solution from 200 ml bottle
You have been provided with one 200ml bottle for each treatment course. Each
contains 200ml of CEP-701 (25mg/ml), so each 80mg dose requires 3.2ml to be
administered. Each bottle should provide up to 60 doses.
1. Remove the metal seal from the vial to expose the rubber stopper.
2. Remove the rubber stopper and insert the yellow adaptor. 3. On the dispenser supplied fix the adhesive line marker at the 3.2ml mark. 4. Insert the dispenser into the yellow cap, carefully turn the vial upside down and withdraw the liquid up to the marked line. 5. Having withdrawn the required 3.2mls, disconnect the dispenser and close the yellow cap till next dose.
Preparation of Diluted CEP-701/Juice Solution and Administration
1. Dispense ENTIRE contents of syringe into plastic dosing cup containing 30 ml
(1 ounce) of approved juice. The following juices or cocktails are approved for use for the administration of the study drug: grape, pineapple, apple, or V8® 100% vegetable juice, orange juice (pulp-free). Do not use grapefruit juice. 2. Mix or stir the solution for approximately 1 minute or until well mixed. Do not shake 3. Drink the diluted solution immediately after mixing. 4. Rinse dosing cup 3 times with 30 ml (1 ounce) of juice and drink juice after each 5. Discard the dosing cup. Version 2: May 2008 Number of Doses Available From Each 200-ml Bottle of CEP-701 Solution
Volume of CEP-701 stock
Maximum number
solution dispensed per
of doses (days)
dosing syringe (ml)
per bottle

The patient/caregiver will prepare each dose as instructed by the study investigator/
research nurse, using the dispenser to withdraw the appropriate volume of CEP-701 as
instructed. Patients/caregivers should be instructed to add the entire contents of the
syringe to 30 ml of the approved juice in a dosing cup. Patients should then drink an
additional 90 ml of juice (3 x 30 ml in the dosing cup). (See above for patient
instructions.) The investigator/research nurse will ensure that the patient/caregiver is
able to demonstrate competence in preparing CEP-701 prior to receiving the drug
supply. CEP-701 may be taken with food. If the patient vomits after receiving a dose,
the dose should not be re-administered and the patient should take the next dose at the
scheduled time. The minimum time between doses is 8 hours.
Solutions of study drug in juice may be stored (protected from light) for up to 1 hour at
room temperature (approximately 20ºC to 25ºC). (Note: for centres outside the US,
solutions of study drug in juice should be stored below 25ºC.) Solutions may be stored
up to 8 hours refrigerated at approximately 2°C to 8°C.
Version 2: May 2008 APPENDIX E: Procedures For Bone Marrow Transplantation
Pre-transplant investigations
Centres will wish to perform their own pre-transplant investigations but the following are
strongly recommended because they may reveal possible contraindications for
proceeding with marrow-ablative therapy.
1.
Bone marrow aspiration to confirm remission (ABSOLUTELY ESSENTIAL) MUGA scan or Echocardiogram Lung function studies
Pre-graft ablative therapy with TBI and cyclophosphamide
The patient should receive allopurinol 300 mg/day for at least two days before the
cyclophosphamide. One of the most distressing and dose-limiting side-effects of
cyclophosphamide is haemorrhagic cystitis. This may be prevented by MESNA, a
compound that inactivates toxic metabolites of cyclophosphamide in the bladder.
Patients should also receive intensive hydration during the giving of cyclophosphamide
and TBI.
Cyclophosphamide
Dosage
Cyclophosphamide is administered at a dose of 60 mg/kg for each of 2 successive days
(use lean body weight for obese patients). It is dissolved in 250 ml of 5% glucose and
administered over 60 min. Following the cyclophosphamide a clear 24 hours should
elapse before TBI commences. The marrow is thawed and reinfused within 24 hours of
completing TBI whether the TBI was given by single or multiple fractions.
MESNA
During cyclophosphamide administration MESNA is given in 4 divided doses by i.v.
push at time 0 (time of commencement of cyclophosphamide), time +3 hours, and +6
and +9 hours. Each dose of MESNA is 40% of the total dose of cyclophosphamide, i.e.
the total MESNA dose is 160% of the total cyclophosphamide dose. Each individual
dose of MESNA must be prescribed separately and the time of administration clearly
noted. The hydration regimen (up to 3l/m2/day), unless used with MESNA, is itself
insufficient to prevent cystitis.
Diuresis
Adequate urine flow must be maintained before and following cyclophosphamide
administration to prevent urate nephropathy and haemorrhagic cystitis. All patients
should receive i.v. fluids at twice the maintenance rate beginning at 6-12 hours before
the cyclophosphamide dose. This will ensure adequate hydration.
Total body irradiation
TBI procedures cannot be completely standardized throughout the UK because of
constraints of machine characteristics and availability. It is recognised that many
schedules in use at present are effective and safe, but the adoption of a limited number
for this study is recommended to make it possible to evaluate the significance of
Version 2: May 2008 fractionation and lung shielding for control of leukaemia and normal tissue toxicity. This
study should not obscure in any way the primary aims of the trial.

Single fraction TBI
• No lung shielding • 1050 cGy if the dose rate is less than 5 cGy per minute. • 950 cGy if the dose rate is 5-10 cGy per minute. • 750 cGy if the dose rate is more than 10 cGy per minute.
Fractionated TBI
• 1440 cGy in 8 fractions over 4 days, 180 cGy per fraction. Treatment will be given using a linear accelerator or cobalt unit operating at the SSD/FSD which gives an adequate, or the largest available, field size. The whole body dose should be defined as the maximum dose to the lung measured by thermoluminescent dosimetry or diodes over 20 minutes for single fraction treatments and for one whole fraction for fractionated treatments. Patient separations will be taken at, and calculation of dose made for, the following sites: Abdomen (at umbilicus)
Additional measurements can be made at the discretion of the participating clinician.
No lung shielding will be used and the prescribed dose will be that to the lung.
Compensators may be used to give homogenous whole body dose if required: doses
will then be measured under compensators. Depth dose data, built up depth and beam
flatness must be determined by phantom measurement at the extended treatment
distance. A central review of machine operating data and calculated doses will be
undertaken.
Note: For patients with initial CNS involvement, additional cranial irradiation
(3 x 200 cGy over 3 to 5 days) will be given before TBI using lateral fields
encompassing the whole brain down to C2 and including the orbit with shielding of the
lens. Additional radiotherapy will not be given to sites of initial bulk disease unless there
is persistent extra-medullary disease in one site only which is not thought to be a
contra-indication to transplantation. A dose of 1000 cGy in 5 fractions will then be given
before TBI.
If you are unable to use TBI ablation please contact one of the transplant coordinators
about possible alternatives.
Sedation and anti-nausea
Combinations of metoclopramide (20 mg i.v.), lorazepam (1-3 mg i.v.), ondansetron (8
mg i.v.) or other 5HT antagonists and dexamethasone (10 mg i.v.) may be used.
Prevention of infection
Specific prophylactic measures are not laid down and procedures may vary slightly from
centre to centre. Infection prophylaxis is of great importance because of the difficulties
in diagnosing and treating infection in immunocompromised patients.
Version 2: May 2008 Infusion of marrow
The marrow should be infused intravenously through a normal giving set. This may be at
any time up to 24 hours following the TBI. Toxicity of the marrow infusion includes
volume overload, pulmonary emboli and allergic reactions.
Other supportive care
Red cell or platelet transfusions will be necessary in the period following the graft. It is
recommended that platelets be given if the peripheral platelet count is less than
10 x 10 /L. All blood products, including platelets, must be irradiated to at least 2500
cGy post transplant. CMV negative recipients should receive CMV negative blood
products whenever possible.
GVHD
Prophylaxis and treatment of graft versus host disease following allo-SCT should follow
the practice of the individual transplant centre.
Version 2: May 2008

APPENDIX F: Derivation of a risk index for younger adults
This appendix gives brief details of the derivation of a risk index for younger adults,
which will be used in AML17 to identify patients suitable to enter the "pick-a-winner"
design. The work has been published (Burnett et al, Blood 2006;108;11:10a (Abstract
18)). It can be viewed as a companion index to the previously developed "Wheatley
index" for elderly patients with AML (Wheatley et al. Blood 2005;106;11:199a (Abstract
674)).
AML is a heterogeneous disease, and prognosis, particularly in younger patients, varies
considerably. Traditionally risk group stratification in MRC AML trials has been based on
cytogenetics and response to the first course of chemotherapy, but this approach does
not take into account variables such as age, white cell count, and performance status
that are known to be prognostic.
As a result, data from the MRC AML10 and AML12 trials (recruiting some 5,400 patients
between 1988 and 2002) were used to construct an index for survival following
complete remission. Because of the design of AML17, where patients with APL are
given separate treatment, these patients were excluded from the analyses. Additionally,
all children were excluded.
The analysis concentrated on clinical parameters which were likely to be available
following the end of the first course of chemotherapy. (For example, in view of the fact
that FLT3 ITD status is only known for a minority of AML10,12 patients, and that FLT3
ITD +ve patients will in any event enter a CEP-701 randomisation, ITD status and other
laboratory markers were not included as candidates for the model).
Using Cox regression, a forward selection model was derived for overall survival from
remission, with the following candidate variables:
Version 2: May 2008 • Performance status • de Novo/Secondary • Cytogenetics (Using Grimwade classification favourable/intermediate/adverse) • Response after course 1 (CR/PR/NR) • Weight The level of significance to enter the model was set at p=0.05. In order of entry to the model, the variables which make up the index are: Variable
The index is therefore:
0.01325*age (in years) + 0.16994*sex (1=male, 0=female) + 0.22131*diagnosis (0=de
novo, 1 secondary) + 0.65082*cytogenetics (1=favourable, 2=intermediate, 3 adverse) +
0.19529*status post C1 (1=CR, 2=PR, 3=NR) + 0.00169* WBC (x109/l)
and the distribution of patients in AML10,12 by index is:
Taking into account the apparent bimodality of the curve, patients with an index of 2 or below were deemed good risk, and the data were arbitrarily divided at the 75th centile Version 2: May 2008 between standard and poor risk. Survival from CR in AML10,12 according to the risk groups was as follows: The index was validated on data from AML15: One important feature of the new risk classification is that the number of poor risk patients has increased. Compared to the old MRC risk classification, the new approach identifies a number of patients who have poor prognosis for reasons other than their cytogenetics: Version 2: May 2008 standard New poor

Appendix G: Supportive Care Recommendations For Acute Promyelocytic
Leukaemia

Version 2: May 2008 (Extract from the BCSH Guideline on the Management of acute myeloid leukaemia in adults) • All-trans retinoic acid (ATRA) should be started as soon as the diagnosis is suspected (grade A; evidence level Ib). • Leucopheresis should be avoided in high count patients (grade B; evidence level • During induction, platelet count should be maintained at >50 × 109/l, together with fresh frozen plasma (FFP) and cryoprecipitate to normalize the activated partial thromboplastin time (APTT) and fibrinogen levels (grade B; evidence level IIb). • ATRA syndrome should be treated promptly with dexamethasone 10 mg twice daily i.v., until the symptoms resolve (grade C; evidence level IV). • Diagnostic work-up should include documentation of underlying PML-RARA fusion (grade B; evidence level IIa). • Patients should undergo molecular monitoring after treatment to guide further therapy (grade B; evidence level IIa). • In case of disease relapse, ATRA should not be used as single agent therapy because of the significant possibility of acquired secondary resistance, and arsenic trioxide (ATO) should only be used in patients with confirmed PML-RARA positive APL (grade B; evidence level IIa). Coagulopathy: A major cause of treatment failure is induction death as a result of
haemorrhage, which reflects to varying degree DIC excessive fibrinolysis and
proteolysis. Patients with higher presenting WBC (i.e. >10 × 109/l) are at highest
risk of haemorrhagic death. Patients with very high presenting leucocyte counts
should not undergo leucopheresis, which may precipitate fatal exacerbation of the
coagulopathy. High rates of induction death have also been observed when low-
dose chemotherapy was used to attempt to reduce WBC in the first instance
(Vahdat et al, 1994). Evidence to date suggests that patients with high presenting
WBC are best commenced on ATRA and anthracycline-based induction therapy.
Haemorrhagic deaths may be reduced by rigorous monitoring of the coagulation
profile and administration of appropriate replacement therapy until morphological
CR has been attained. APTT, prothrombin time, thrombin time, fibrinogen level
and platelet count should be checked at least twice daily during the early stages of
treatment. Coagulation times should be kept within the normal range using FFP as
replacement. Fibrinogen levels may be low due to DIC and cryoprecipitate should
be given as replacement aiming for a level of approximately 2 g/l. Elevated levels
of fibrinogen should be avoided because of the increased risk of thrombosis
associated with APL, which may be further exacerbated by ATRA. The platelet
count should ideally be maintained above 50 × 109/l until morphological remission
has been confirmed. Clinical studies have not established proven benefit for use of
heparin or anti-fibrinolytic agents as a means of decreasing induction death rates
in APL and their routine use is not recommended. Indeed, anti-fibrinolytic agents
when combined with ATRA could potentially increase the inherent risk of
Version 2: May 2008 thrombotic complications. Nevertheless, anti-fibrinolytic agents could be contemplated in situations of life-threatening haemorrhage in the presence of normal coagulation assays. Recombinant activated Factor VII has also been used in the context of potentially fatal haemorrhage (Alimoghaddam K et al, 2006). Differentiation syndrome: (see Section 19.8.1)
Version 2: May 2008

Source: http://aml17.cardiff.ac.uk/files/aml17_protocolv2.pdf