Standard vs. Reduced-Intensity Conditioning in Patients With Acute Myeloid Leukemia in First Remission
Acute Myeloid Leukemia
About this trial
This is an interventional treatment trial for Acute Myeloid Leukemia focused on measuring Reduced-intensity conditioning, Fludarabine, Acute myeloid Leukemia, Treatment-related mortality
Eligibility Criteria
Inclusion Criteria: Diagnosis of acute myeloid leukemia in first remission Standard-or high-risk marrow cytogenetics HLA-matched related or unrelated donor available (in case of high-risk disease) Age 18 to 60 Informed consent Consent of donor to donate peripheral blood stem cells sufficient liver function (elevation of transferases < 2.5 x upper limit) Exclusion Criteria: AML with t(5;17) AML with t((8;21) clinically relevant heart failure (NYHA II-IV) Renal failure (creatinine > 200 µg/ml) Liver function failure (bilirubin > 3 mg/dl) Concomitant Neurological or psychiatric disease Contraindications to receive prescribed study medication HIV infection Pregnancy
Sites / Locations
- Medizinische Klinik und Poliklinik I
Arms of the Study
Arm 1
Arm 2
Other
Experimental
12 Gy/Cyclophosphamide
8 Gy /Fludarabine
Standard intensity conditioning
Reduced-intensity conditioning