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氟达拉滨和阿糖胞苷与高剂量阿糖胞苷在 t(8;21) 急性髓系白血病巩固治疗中的比较:一项前瞻性、随机研究。

Fludarabine and cytarabine versus high-dose cytarabine in consolidation treatment of t(8; 21) acute myeloid leukemia: A prospective, randomized study.

机构信息

Department of Hematology, Institute of Hematology, Changhai Hospital, Shanghai, China.

Department of Hematology, Shanghai Jiao Tong University Affiliated First People's Hospital, Shanghai, China.

出版信息

Am J Hematol. 2017 Jan;92(1):12-17. doi: 10.1002/ajh.24569. Epub 2016 Oct 21.

Abstract

Acute myeloid leukemia (AML) patients with t(8;21) aberration often have favorable outcomes, however, relapse still occurs in 30-40% patients, with only 50-60% of patients with t(8;21) AML cured with regimens containing high-dose cytarabine (HD-Ara-C). To evaluate the effects of fludarabine and cytarabine (FA) consolidation therapy for t(8;21) AML patients, a prospective randomized study was performed. A total of 45 patients with t(8;21) AML after achieving complete remission (CR) were randomly assigned to receive four course consolidation with FA (n = 23) or HD-Ara-C (n = 22). Our study showed that at 36-months, relapse-free survival (RFS) was 81.73% in the FA arm and 50.73% in the HD-Ara-C arm (P = 0.04), overall survival (OS) was 91.1% and 48.4% (P = 0.01) in the FA arm and in the HD-Ara-C arm respectively; whereas cumulative incidence of relapse (CIR) was 18.27% and 47.39%, in the FA arm and in the HD-Ara-C arm respectively (P = 0.05). In our study, treatment with FA, MRD2 status (reduction ≥ 3-log) and absence of c-kit mutations were identified as independent prognostic factors for lower risk of relapse, improved RFS and OS. We also found RFS for patients without c-kit mutations was 100% in FA arm, and 57.8% in HD-Ara-C arm at 36 months (P = 0.005); OS of both groups at 36 months was 100% and 51.4%, respectively (P = 0.004), suggesting a benefit of consolidation therapy with FA for t(8;21) AML patients, especially, those without c-kit mutations (Clinicaltrials.org ID NCT# 02024308). Am. J. Hematol. 92:12-17, 2017. © 2016 Wiley Periodicals, Inc.

摘要

急性髓系白血病(AML)伴 t(8;21)异常的患者通常预后良好,但仍有 30-40%的患者复发,仅 50-60%伴 t(8;21)AML 的患者采用含高剂量阿糖胞苷(HD-Ara-C)的方案治愈。为评估氟达拉滨和阿糖胞苷(FA)巩固治疗 t(8;21)AML 患者的效果,进行了一项前瞻性随机研究。共有 45 例完全缓解(CR)后伴 t(8;21)AML 的患者被随机分配接受 4 个疗程的 FA(n=23)或 HD-Ara-C(n=22)巩固治疗。我们的研究表明,36 个月时,FA 组无复发生存率(RFS)为 81.73%,HD-Ara-C 组为 50.73%(P=0.04),FA 组总生存率(OS)为 91.1%,HD-Ara-C 组为 48.4%(P=0.01);而 FA 组和 HD-Ara-C 组的累积复发率(CIR)分别为 18.27%和 47.39%(P=0.05)。在我们的研究中,FA 治疗、MRD2 状态(降低≥3 对数)和无 c-kit 突变被确定为复发风险较低、RFS 和 OS 改善的独立预后因素。我们还发现,FA 组无 c-kit 突变的患者 36 个月时的 RFS 为 100%,HD-Ara-C 组为 57.8%(P=0.005);两组 36 个月时的 OS 分别为 100%和 51.4%(P=0.004),表明 t(8;21)AML 患者接受 FA 巩固治疗,特别是无 c-kit 突变的患者,有获益(Clinicaltrials.org 注册号 NCT#02024308)。美国血液学杂志 92:12-17,2017。版权所有©2016 威利父子公司。

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