Efficacy and safety of venetoclax plus azacitidine based regimens in the treatment of relapsed or refractory acute myeloid leukemia: a systematic review and meta-analysis

维奈托克联合阿扎胞苷方案治疗复发或难治性急性髓系白血病的疗效和安全性:系统评价和荟萃分析

阅读:1

Abstract

This meta-analysis aimed to evaluate the efficacy and safety of venetoclax plus azacitidine (VEN + AZA) regimens in patients with relapsed or refractory acute myeloid leukemia (R/R AML) and to explore the effects of different combination strategies, including chemotherapy and targeted agents, on clinical outcomes. A systematic search of PubMed, Web of Science, Embase, and Cochrane Library databases was performed up to February 2025. Studies that reported complete remission or complete remission with incomplete hematologic recovery (CR/CRi) were included. Study quality was assessed using the Newcastle-Ottawa Scale (NOS) for Non-Randomized Controlled Trials (NRCTs). Pooled estimates were calculated using random-effects models, and subgroup analyses were performed. The CR/CRi rate for VEN + AZA-based regimens was 43% (95% CI: 33-53%), with substantial heterogeneity (I²=89.20%). Subgroup analysis indicated higher CR/CRi rates for VEN + AZA combined with chemotherapy (68%, 95% CI: 62-73%) compared to VEN + AZA alone (38%, 95% CI: 28-47%) or VEN + AZA with targeted agents (28%, 95% CI: 18-40%). The most common grade ≥ 3 adverse events were neutropenia (89%) and thrombocytopenia (82%). VEN + AZA combined with chemotherapy significantly improved CR/CRi rates in R/R AML compared to VEN + AZA alone or with targeted agents.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。