Overview
Study of Busulfan and FLAG Conditioning Regimen for Allogeneic Peripheral Blood Stem Cell Transplantation
Status:
Unknown status
Unknown status
Trial end date:
2020-07-01
2020-07-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to determine the safety and efficacy of Busulfan/FLAG (fludarabine, cytarabine and granulocyte colony-stimulating factor) Conditioning Regimen in Patients with Relapsed/refractory Acute Leukemia undergoing allogeneic peripheral blood stem cell transplantation.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Chinese PLA General HospitalCollaborators:
309th Hospital of Chinese People's Liberation Army
Beijing Naval General Hospital
Space Center Hospital, Peking UniversityTreatments:
Busulfan
Cytarabine
Fludarabine
Fludarabine phosphate
Lenograstim
Sargramostim
Thymoglobulin
Vidarabine
Criteria
Inclusion Criteria:- relapsed/refractory acute leukemia regardless of cytogenetics
- All patients should aged 12 to 65 years
- Have matched sibling donors, ≥8/10 HLA(human leukocyte antigen) matched unrelated
donors or haploidentical donors
- Patients without any uncontrolled infections or without severe pulmonary, renal,
hepatic or cardiac diseases
Exclusion Criteria:
- Patients aged less than 12 years old
- Patients with any uncontrolled infections or with severe pulmonary, renal, hepatic or
cardiac diseases
- Acute myeloid leukemia patients with t (15;17)