Study of Low-Dose Intravenous Decitabine in Patients Aged > 60 Years With Acute Myeloid Leukemia

Hypothesis: If after 4 courses of Decitabine none out of 12 patients achieves a response (complete or partial remission, antileukemic effect), the protocol will be stopped. If at least one response is seen among the first 12 patients, 17 additional patients will be treated in an open, uncontrolled manner. If in 3 or more of these 29 patients a response is achieved, this treatment will be considered effective and will be studied further, otherwise it will be considered ineffective. At a preliminary analysis after recruitment of 29 patients, encouraging results (response rate, tolerability) are prompting continuation of recruitment, with a planned inclusion of at least 60 patients, until initiation of the planned large, controlled phase II follow-up trial. Unexpected toxicities will be carefully evaluated. 29 patients were needed for the first two steps of this phase II study, at least 60 patients are planned for the extension of the recruitment. Expected study duration for the first two steps was 15-20 months, with 35-40 months total when including the third step.

Inclusion criteria

• Patients older than 60 years with acute myeloid leukemia (> 30 % bone marrow blasts) not qualifying for, or not consenting to, standard induction chemotherapy or immediate allografting
• life expectancy > 3 months with successful treatment
• performance status ECOG 0, 1, 2
• age-adjusted normal cardiac, kidney, liver function (creatinine < 1.5 mg/dl unless leukemia-related, total bilirubin < 2.0 of upper normal limits)
• patients with >50 000 leukocytes/µl in whom initial cytoreduction according to protocol is effective
• written informed consent

Exclusion criteria

• AML of FAB subtype M3
• previous induction-type chemotherapy for MDS or AML
• previous treatment with Decitabine, 5-azacytidine or ATRA
• "low-dose" chemotherapy (e.g.hydroxyurea, cytosine arabinoside, melphalan) within 8 weeks prior to Decitabine treatment, except for cytoreduction of leukocytosis > 50 000/µl according to protocol - patients with > 50 000 leukocytes/µl in whom initial cytoreduction according to protocol is ineffective
• treatment with cytokines within previous 4 weeks
• concomitant use of any other investigational drug
• other malignancy that is not in remission (previous chemotherapy for other malignancies is not an exclusion criteria)
• cardiac insufficiency NYHA IV
• HIV infection
• other uncontrolled active infection
• psychiatric disorder that interferes with treatment
• known hypersensitivity to retinoids
• contact lenses