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.
Eun-Ji ChoiJe Hwan LeeHawk KimYunsuk ChoiWon-Sik LeeSang-Min LeeJun-Hong ParkHan-Seung ParkJung-Hee LeeKyoo-Hyung Leenull nullPublished in: International journal of hematology (2021)
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.
Keyphrases
- acute myeloid leukemia
- free survival
- high dose
- allogeneic hematopoietic stem cell transplantation
- low dose
- stem cell transplantation
- disease activity
- end stage renal disease
- ulcerative colitis
- chronic kidney disease
- cell therapy
- cardiovascular events
- newly diagnosed
- ejection fraction
- type diabetes
- study protocol
- coronary artery disease
- high throughput
- metabolic syndrome
- squamous cell carcinoma
- phase iii
- platelet rich plasma
- risk factors
- patient reported outcomes
- binding protein
- cross sectional
- acute lymphoblastic leukemia