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复发/难治性 AML 中去甲基化药物:大型国际患者队列中的结果及其预测因素。

Hypomethylating agents in relapsed and refractory AML: outcomes and their predictors in a large international patient cohort.

机构信息

Section of Hematology, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT.

Department of Biostatistics, Yale School of Public Health, New Haven, CT.

出版信息

Blood Adv. 2018 Apr 24;2(8):923-932. doi: 10.1182/bloodadvances.2018016121.

DOI:10.1182/bloodadvances.2018016121
PMID:29685952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5916007/
Abstract

Although hypomethylating agents (HMAs) are frequently used in the frontline treatment of older acute myeloid leukemia (AML) patients, little is known about their effectiveness in relapsed or primary treatment-refractory (RR)-AML. Using an international multicenter retrospective database, we studied the effectiveness of HMAs in RR-AML and evaluated for predictors of response and overall survival (OS). A total of 655 patients from 12 centers received azacitidine (57%) or decitabine (43%), including 290 refractory (44%) and 365 relapsed (56%) patients. Median age at diagnosis was 65 years. Best response to HMAs was complete remission (CR; 11%) or CR with incomplete count recovery (CRi; 5.3%). Additionally, 8.5% experienced hematologic improvement. Median OS was 6.7 months (95% confidence interval, 6.1-7.3). As expected, OS differed significantly by best response, with patients achieving CR and CRi having a median OS of 25.3 and 14.6 months, respectively. In multivariate analysis, the presence of ≤5% circulating blasts and a 10-day schedule of decitabine were associated with improved response rates, whereas the presence of >5% circulating blasts and >20% bone marrow blasts were associated with decreased OS. A significant subset of RR-AML patients (16%) achieved CR/CRi with HMAs and experienced a median OS of 21 months. Outside of a clinical trial, HMAs represent a reasonable therapeutic option for some patients with RR-AML.

摘要

虽然低甲基化剂(HMAs)经常被用于治疗老年急性髓系白血病(AML)患者的一线治疗,但对于它们在复发或原发性治疗抵抗(RR)-AML 中的疗效知之甚少。我们使用国际多中心回顾性数据库研究了 HMAs 在 RR-AML 中的疗效,并评估了其缓解率和总生存期(OS)的预测因素。来自 12 个中心的 655 例患者接受了阿扎胞苷(57%)或地西他滨(43%)治疗,包括 290 例难治(44%)和 365 例复发(56%)患者。诊断时的中位年龄为 65 岁。HMAs 的最佳反应为完全缓解(CR;11%)或不完全血细胞计数恢复的 CR(CRi;5.3%)。此外,有 8.5%的患者出现血液学改善。中位 OS 为 6.7 个月(95%置信区间,6.1-7.3)。正如预期的那样,OS 根据最佳反应显著不同,达到 CR 和 CRi 的患者的中位 OS 分别为 25.3 和 14.6 个月。在多变量分析中,存在≤5%的循环白血病细胞和 10 天的地西他滨方案与提高缓解率相关,而存在>5%的循环白血病细胞和>20%的骨髓白血病细胞与降低 OS 相关。RR-AML 患者中有一个显著的亚组(16%)用 HMAs 达到 CR/CRi,并经历了中位 OS 为 21 个月。在临床试验之外,HMAs 代表了一些 RR-AML 患者的合理治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b02/5916007/a245dd3cb954/advances016121absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b02/5916007/a245dd3cb954/advances016121absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b02/5916007/a245dd3cb954/advances016121absf1.jpg

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