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Autologous hematopoietic cell transplantation following high-dose cytarabine consolidation for core-binding factor-acute myeloid leukemia in first complete remission: a phase 2 prospective trial
被引:0
|作者:
Eun-Ji Choi
Je-Hwan Lee
Hawk Kim
Yunsuk Choi
Won-Sik Lee
Sang-Min Lee
Jun-Hong Park
Han-Seung Park
Jung-Hee Lee
Kyoo-Hyung Lee
机构:
[1] University of Ulsan College of Medicine,Department of Hematology, Asan Medical Center
[2] Gachon University Gil Medical Center,Division of Hematology
[3] Gachon University College of Medicine,Department of Hematology and Oncology
[4] Ulsan University Hospital,Department of Hematology and Oncology, Busan Paik Hospital
[5] University of Ulsan College of Medicine,undefined
[6] Inje University College of Medicine,undefined
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关键词:
Core-binding factor;
Acute myeloid leukemia;
Autologous hematopoietic cell transplantation;
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摘要:
Core-binding factor (CBF)-acute myeloid leukemia (AML) generally have a favorable prognosis. However, approximately 50% of patients experience disease relapse during or after post-remission therapy. Retrospective studies on autologous hematopoietic cell transplantation (AHCT) have shown improved survival with decreased relapse rate in CBF-AML. In this prospective study, we evaluate the outcomes of AHCT following high-dose cytarabine (HiDAC) consolidation in patients with CBF-AML in first complete remission (CR). Adult patients with CBF-AML achieving first CR after induction chemotherapy were eligible for the study. High-dose chemotherapy before AHCT included intravenous busulfan (3.2 mg/kg/day, days − 7 to − 5) and etoposide (400 mg/m2/day, days − 3 to − 2). Twenty-nine patients, 17 with t(8;21) and 12 with inv(16), underwent AHCT following 2 or 3 courses of HiDAC consolidation. The estimated 5-year overall and disease-free survival rates were between 89.0% and 82.5%, respectively. The cumulative incidences of relapse and non-relapse mortality were between 17.5% and 0%, respectively. Presence of measurable residual disease (MRD) before AHCT and KIT mutation were significantly associated with relapse after transplantation. In conclusion, the post-remission strategy of AHCT following HiDAC consolidation in CBF-AML was feasible and efficacious. Assays for MRD and KIT mutation may guide selection of patients who will benefit from AHCT in CBF-AML in first CR.
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页码:851 / 860
页数:9
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