Randomized Study of Conditioning of Fludarabine Combined With Single or Dual Alkylating Agents in Myeloid Malignancies
Acute Myeloid Leukemia, Myelodysplastic Syndromes
About this trial
This is an interventional treatment trial for Acute Myeloid Leukemia focused on measuring conditioning regimen, melphalan, busulfan, fludarabine
Eligibility Criteria
Inclusion Criteria: acute myeloid leukemia (acute promyelocytic leukemia excluded) in 1st complete remission myelodysplasia syndrome with bone marrow blast >5% and remaining less than 20% at transplantation patients with HLA matched sibling donor, 9-10 matched unrelated donor or haplo-identical related donors inform consent provided Exclusion Criteria: AML patients with active CNS or extramedullary diseases patients with active viral, bacterial or fungal infection patients with hepatitis B virus >1X103 copy/ml patients with abnormal liver function, renal function, respiratory or cardiac dysfunction patients with uncontrolled mental disorders patients with HIV
Sites / Locations
- Fujian Medical University Union HospitalRecruiting
- Zhongshan Hospital, Xianmen UniversityRecruiting
- 923th Hospital PLARecruiting
- First Affiliatied Hospital of Soochow UniversityRecruiting
- First Affiliated Hospital of Nanjin Medical UnviersityRecruiting
- Ruijin HospitalRecruiting
- Shanghai No10 HospitalRecruiting
- 920th Hospital PLARecruiting
- Shanghai No 6 HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Flu-Bu2-Mel140
Flu-Bu4
Patients receive fludarabine, busulfan and melphalan as conditioning regimen
Patients receive fludarabine and busulfan as conditioning regimen