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高剂量阿糖胞苷巩固治疗后自体造血细胞移植治疗初诊完全缓解的核心结合因子急性髓系白血病:一项 2 期前瞻性试验。

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.

机构信息

Department of Hematology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Korea.

Division of Hematology, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Korea.

出版信息

Int J Hematol. 2021 Jun;113(6):851-860. doi: 10.1007/s12185-021-03099-6. Epub 2021 Mar 2.

Abstract

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/m/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.

摘要

核心结合因子 (CBF)-急性髓系白血病 (AML) 一般具有较好的预后。然而,约有 50%的患者在缓解后或缓解后治疗期间发生疾病复发。自体造血细胞移植 (AHCT) 的回顾性研究表明,在 CBF-AML 中,接受 AHCT 可提高生存率并降低复发率。在这项前瞻性研究中,我们评估了在 CBF-AML 患者首次完全缓解 (CR) 后接受高剂量阿糖胞苷 (HiDAC) 巩固治疗后行 AHCT 的结果。诱导化疗后达到首次 CR 的 CBF-AML 成年患者符合研究条件。AHCT 前的高剂量化疗包括静脉用白消安 (3.2mg/kg/天,第 -7 天至 -5 天) 和依托泊苷 (400mg/m/天,第 -3 天至 -2 天)。29 例患者,17 例有 t(8;21),12 例有 inv(16),在接受 2 或 3 个疗程的 HiDAC 巩固治疗后接受 AHCT。估计 5 年总生存率和无病生存率分别为 89.0%和 82.5%。复发和非复发死亡率的累积发生率分别为 17.5%和 0%。移植前存在可测量残留疾病 (MRD) 和 KIT 突变与移植后复发显著相关。总之,在 CBF-AML 中,在 HiDAC 巩固治疗后行 AHCT 的缓解后策略是可行且有效的。MRD 和 KIT 突变的检测可能有助于指导在 CBF-AML 首次 CR 中选择从 AHCT 中获益的患者。

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