[selinexor联合venetoclax和阿扎胞苷诱导治疗复发和难治性急性髓性白血病的临床安全性和有效性]。

Q3 Medicine
L N Liu, Y S Cui, Y Z Liu, Y M Wang, P Xiang, L J Liang, Y R Li, B J Fang
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引用次数: 0

摘要

目的:确定西利奈德联合韦尼替克雷克斯(VEN)和阿扎替丁(AZA)治疗复发性和/或难治性急性髓性白血病(R/R AML)患者的疗效和安全性。研究纳入了2022年5月至2023年5月在郑州大学附属肿瘤医院接受西利奈克索联合VEN和AZA治疗的12例R/R急性髓性白血病患者。对他们的临床数据进行了回顾性分析。在12例R/R急性髓细胞白血病患者中,5例(41.7%)达到完全缓解(CR),1例(8.3%)达到CR但血液学未完全恢复,5例(41.7%)达到部分缓解。达到CR的中位时间为28(16-59)天。中位PFS为61(15-300)天。该方案的主要不良反应是血液学毒性。没有观察到与化疗相关的死亡病例。西利奈索加VEN和AZA联合疗法是治疗R/R急性髓细胞白血病患者的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The clinical safety and efficacy of selinexor combined with venetoclax and azactitidine induction therapy in relapsed and refractory acute myeloid leukemia].

To determine the efficacy and safety of selinexor combined with venetoclax (VEN) and azactitidine (AZA) for patients with relapsed and/or refractory acute myeloid leukemia (R/R AML) . Twelve patients with R/R AML treated with selinexor plus VEN and AZA in the Affiliated Cancer Hospital of Zhengzhou University from May 2022 to May 2023 were included. Their clinical data were retrospectively analyzed. Among the 12 R/R AML patients, 5 (41.7%) achieved complete remission (CR) , 1 (8.3%) achieved CR with incomplete hematological recovery, and 5 (41.7%) achieved partial remission. The median time to reach CR was 28 (16-59) days. The median PFS was 61 (15-300) days. The main adverse event of the regimen was hematological toxicity. No chemotherapy-related deaths were observed. The combination of selinexor plus VEN and AZA is an effective treatment for R/R AML patients.

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CiteScore
0.80
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