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75 岁及以上急性髓系白血病患者一线应用去甲基化药物联合 Venetoclax 的临床结局:来自美国 8 家学术中心的真实世界数据。

Clinical outcomes of hypomethylating agents plus Venetoclax as frontline treatment in patients 75 years and older with acute myeloid leukemia: Real-world data from eight US academic centers.

机构信息

Division of Hematology and Oncology, Leukemia Program, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.

出版信息

Am J Hematol. 2024 Apr;99(4):606-614. doi: 10.1002/ajh.27231. Epub 2024 Feb 11.

Abstract

Venetoclax (VEN) combined with hypomethylating agents (HMAs) is the standard of care for the treatment of patients with newly diagnosed acute myeloid leukemia (AML) unfit for intensive chemotherapy. To date, real-world data published on HMAs plus VEN have been either single-center studies or using community-based electronic databases with limited details on mutational landscape, tolerability, and treatment patterns in elderly patients. Therefore, we conducted a multicenter retrospective study to assess the real-world experience of 204 elderly patients (≥75 years) with newly diagnosed AML treated with HMAs plus VEN from eight academic centers in the United States. Overall, 64 patients achieved complete remission (CR; 38%) and 43 CR with incomplete count recovery (CRi; 26%) for a CR/CRi rate of 64%, with a median duration of response of 14.2 months (95% CI: 9.43, 22.1). Among responders, 63 patients relapsed (59%) with median overall survival (OS) after relapse of 3.4 months (95% CI, 2.4, 6.7). Median OS for the entire population was 9.5 months (95% CI, 7.85-13.5), with OS significantly worse among patients with TP53-mutated AML (2.5 months) and improved in patients harboring NPM1, IDH1, and IDH2 mutations (13.5, 18.3, and 21.1 months, respectively). The 30-day and 60-day mortality rates were 9% and 19%, respectively. In conclusion, HMAs plus VEN yielded high response rates in elderly patients with newly diagnosed AML. The median OS was inferior to that reported in the VIALE-A trial. Outcomes are dismal after failure of HMAs plus VEN, representing an area of urgent unmet clinical need.

摘要

维奈托克(VEN)联合低甲基化药物(HMAs)是治疗不适合强化化疗的新诊断急性髓系白血病(AML)患者的标准治疗方法。迄今为止,已发表的关于 HMA 加 VEN 的真实世界数据要么是单中心研究,要么是使用社区为基础的电子数据库,这些数据对突变景观、耐受性和老年患者的治疗模式的详细信息有限。因此,我们进行了一项多中心回顾性研究,以评估 204 名来自美国 8 个学术中心的新诊断 AML 老年患者(≥75 岁)接受 HMA 加 VEN 治疗的真实世界经验。总体而言,64 名患者达到完全缓解(CR;38%)和 43 名不完全计数恢复的 CR(CRi;26%),CR/CRi 率为 64%,反应持续时间中位数为 14.2 个月(95%CI:9.43,22.1)。在应答者中,63 名患者复发(59%),复发后中位总生存期(OS)为 3.4 个月(95%CI,2.4,6.7)。整个人群的中位 OS 为 9.5 个月(95%CI,7.85-13.5),TP53 突变 AML 患者的 OS 明显较差(2.5 个月),而 NPM1、IDH1 和 IDH2 突变患者的 OS 得到改善(分别为 13.5、18.3 和 21.1 个月)。30 天和 60 天死亡率分别为 9%和 19%。总之,HMAs 加 VEN 治疗新诊断 AML 的老年患者取得了较高的反应率。中位 OS 低于 VIALE-A 试验报告的结果。HMAs 加 VEN 失败后预后较差,代表了一个迫切需要满足的临床需求领域。

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