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老年急性髓系白血病患者非强化治疗方案的治疗模式和对比分析——来自印度的真实世界经验。

Treatment patterns and comparative analysis of non-intensive regimens in elderly acute myeloid leukemia patients-a real-world experience from India.

机构信息

Department of Medical Oncology, Kidwai Memorial Institute of Oncology, Bangalore, Karnataka, 560029, India.

出版信息

Ann Hematol. 2019 Apr;98(4):881-888. doi: 10.1007/s00277-019-03600-6. Epub 2019 Jan 29.

Abstract

Elderly patients with acute myeloid leukemia have a poor prognosis. Data from developing countries is sparse in the literature. In this retrospective study, 402 patients aged ≥ 60 years, diagnosed between Jan 2013 and Dec 2017, were analyzed for treatment patterns and survival. Median age of the whole cohort was 68 years (range 61-84). A total of 213 patients (53.3%) refused care; 188 patients (46.7%) received either BSC, LDAC, or HMA. Survival (in months) was 3.9, 6.4, and 1.2 with LDAC, HMA, and BSC, respectively. One-year survival was 17.2% and 6% with HMA and LDAC, respectively (P = 0.02). Overall response rate (ORR) did not differ between HMA and LDAC group (p = 0.12). HMA cohort had higher complete responses (20.6% vs 7.4%, p = 0.02), stable disease (32.7% vs 13.5%, p = 0.02), and transfusion independence (TI) (46.5% vs 22.2%, p = 0.01). Survival did not differ between the groups if the patients achieved ORR (12.3 vs 9.8 p = 0.2) or TI (11.6 vs 6.4 p = 0.2). Stable disease with HMA led to longer survival (8.1 vs 5.3 p = 0.01). HMAs were more effective than LDAC irrespective of cytogenetic risk category and blasts, of note HMAs improved survival of poor risk patients (5.6 vs 2.9 p = 0.004). HMA treatment (HR = 0.48; 95% 0.29-0.79, p = 0.004) and transfusion independence (HR = 0.2; 95% 0.1-0.3, p = 0.0001) predicted survival in multivariate analysis. Neutropenia and febrile neutropenia were frequent in HMA. Thrombocytopenia was the common adverse event with LDAC. Novel and cost-effective drugs are essential to improve the prognosis of these patients.

摘要

老年急性髓系白血病患者预后较差。发展中国家的数据在文献中较为匮乏。在这项回顾性研究中,分析了 2013 年 1 月至 2017 年 12 月期间诊断为年龄≥60 岁的 402 例患者的治疗模式和生存情况。全队列的中位年龄为 68 岁(范围 61-84)。共有 213 例患者(53.3%)拒绝治疗;188 例患者(46.7%)接受了 BSC、LDAC 或 HMA 治疗。LDAC、HMA 和 BSC 治疗的生存(月)分别为 3.9、6.4 和 1.2。HMA 和 LDAC 组的 1 年生存率分别为 17.2%和 6%(P=0.02)。HMA 和 LDAC 组的总体缓解率(ORR)无差异(p=0.12)。HMA 组完全缓解率(20.6%比 7.4%,p=0.02)、稳定疾病率(32.7%比 13.5%,p=0.02)和输血独立性(TI)率(46.5%比 22.2%,p=0.01)更高。如果患者达到 ORR(12.3%比 9.8%,p=0.2)或 TI(11.6%比 6.4%,p=0.2),两组的生存情况无差异。HMA 诱导的稳定疾病可延长生存(8.1 比 5.3,p=0.01)。HMAs 比 LDAC 更有效,无论细胞遗传学风险类别和原始细胞百分比如何,值得注意的是,HMAs 改善了高危患者的生存(5.6 比 2.9,p=0.004)。多因素分析显示,HMA 治疗(HR=0.48;95%CI 0.29-0.79,p=0.004)和输血独立性(HR=0.2;95%CI 0.1-0.3,p=0.0001)可预测生存。HMA 组常出现中性粒细胞减少和发热性中性粒细胞减少。血小板减少是 LDAC 的常见不良事件。新型、具有成本效益的药物对于改善这些患者的预后至关重要。

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