The aim of this study is to determine the therapeutic efficacy of Decitabine in patients with chronic myelomonocytic leukemia (CMML) diagnosis according to WHO criteria either untreated or previously treated with Hydrea or Etoposide (given orally), non intensive chemotherapy or intensive chemotherapy given more than 3 months before inclusion.
Study Type
INTERVENTIONAL
Allocation
NA
Enrollment
41
20mg/m2/day, one hour intravenous infusion, every day during 5 days
CHR La Source orléans
Orléans, Orléans, France
To determine response of patients with CMML to 6 courses of Decitabine according to IWG 2006 criteria, adapted for CMML with WBC>12000/mm3
Response duration
Time to progression to AML
Survival
Toxicity (hematological and non-hematological)
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