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口服三氧化二砷为基础的维持治疗方案用于急性早幼粒细胞白血病首次完全缓解:一项 10 年随访研究。

Oral arsenic trioxide-based maintenance regimens for first complete remission of acute promyelocytic leukemia: a 10-year follow-up study.

机构信息

Department of Medicine, Queen Mary Hospital, Pokfulam Road,Hong Kong, China.

出版信息

Blood. 2011 Dec 15;118(25):6535-43. doi: 10.1182/blood-2011-05-354530. Epub 2011 Oct 12.

DOI:10.1182/blood-2011-05-354530
PMID:21998212
Abstract

Seventy-six patients with acute promyelocytic leukemia (APL) in first complete remission after induction and consolidation by daunorubicin and cytosine arabinoside received oral arsenic trioxide (As(2)O(3))-based maintenance. Three regimens were used: oral As(2)O(3) (10 mg/day, regimen A, n = 20), oral As(2)O(3) plus all-trans retinoic acid (ATRA, 45 mg/m(2) per day, regimen AA, n = 19), and oral As(2)O(3) plus ATRA plus ascorbic acid (1000 mg/day, regimen AAA, n = 37), each given for 2 weeks every 2 months for 2 years. Patients receiving A, AA, and AAA maintenance did not differ significantly in clinicopathologic features and risk factors. Headache, dyspepsia, reversible liver function derangement, and herpes zoster reactivation were adverse effects observed during maintenance. QTc prolongation and arrhythmias were not encountered. At a median follow-up of 24 months (range, 1-115 months), there were 8 relapses. The 3-year leukemia-free-survival, event-free-survival, and overall-survival were 87.7%, 83.7%, and 90.6%, respectively. Adverse prognostic factors included male gender for leukemia-free-survival, and unrelated cancers for overall survival. Age, presentation WBC count and platelet count, and the type of oral As(2)O(3) maintenance regimens had no impact on survivals. Prolonged oral As(2)O(3) maintenance was feasible and safe and resulted in favorable outcomes when used with a simple induction and consolidation regimen compared with other protocols composed of multiple chemotherapeutic agents.

摘要

76 例急性早幼粒细胞白血病(APL)患者在诱导和巩固治疗使用柔红霉素和阿糖胞苷后达到完全缓解,接受了口服三氧化二砷(As2O3)维持治疗。使用了三种方案:口服 As2O3(10mg/天,方案 A,n=20)、口服 As2O3 加全反式维甲酸(ATRA,45mg/m2/天,方案 AA,n=19)和口服 As2O3 加 ATRA 加抗坏血酸(1000mg/天,方案 AAA,n=37),每个方案每 2 个月给药 2 周,持续 2 年。接受 A、AA 和 AAA 维持治疗的患者在临床病理特征和危险因素方面无显著差异。在维持治疗期间观察到头痛、消化不良、可逆肝功能异常和带状疱疹再激活等不良反应。未发生 QTc 延长和心律失常。中位随访时间为 24 个月(范围,1-115 个月),有 8 例复发。3 年无白血病生存率、无事件生存率和总生存率分别为 87.7%、83.7%和 90.6%。不良预后因素包括无白血病生存率的男性性别和总生存率的无关癌症。年龄、初诊白细胞计数和血小板计数以及口服 As2O3 维持方案的类型对生存无影响。与其他包含多种化疗药物的方案相比,使用简单的诱导和巩固方案,延长口服 As2O3 维持治疗是可行且安全的,可获得良好的结果。

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