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维奈托克联合去甲基化药物治疗复发/难治性急性髓系白血病的反应和生存的临床及分子预测因素:一项针对中国患者的单中心研究

Clinical and Molecular Predictors of Response and Survival Following Venetoclax Plus Hypomethylating Agents in Relapsed/Refractory Acute Myeloid Leukemia: A Single-Center Study in Chinese Patients.

作者信息

Wang Linya, Gao Haitao, Fu Qiang, Jiang Qian, Jiang Hao, Wang Yu, Xu Lanping, Zhang Xiaohui, Huang Xiaojun, Tang Feifei

机构信息

Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University, Beijing 100044, China.

Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.

出版信息

Cancers (Basel). 2025 Feb 8;17(4):586. doi: 10.3390/cancers17040586.

Abstract

PURPOSE

This study aimed to investigate the efficacy and the clinical and molecular predictors of response and survival following venetoclax plus hypomethylating agents (VEN + HMAs) in adult relapsed/refractory acute myeloid leukemia (R/R AML) patients.

METHODS

We retrospectively analyzed 197 adult R/R AML patients who received the VEN + HMAs regimen. Molecular profiling was performed using targeted next-generation sequencing (NGS) of 139 genes to explore potential response and survival genetic predictors.

RESULTS

The median treatment cycle was 1 (1-4) cycle. The composite complete remission (CRc) rate, encompassing complete remission (CR) and CR with incomplete hematologic recovery (CRi), was 44.7%, while the overall response rate (ORR) reached 59.9%. With a median follow-up period of 14.0 months (range: 0.7-54.0 months), the 1-year and 2-year overall survival (OS) rates were 55.4% and 40.2%, respectively. Multivariate analyses revealed that mutations in and were significantly associated with improved response rates. Conversely, prior exposure to HMA therapy, early relapse, and the presence of mutations were linked to lower response rates. Regarding survival outcomes, the fusion gene, as well as mutations in and , were found to be favorable prognostic factors for OS, whereas mutations in , , , and were associated with worse OS.

CONCLUSIONS

The VEN + HMAs regimen demonstrated considerable efficacy in the treatment of R/R AML patients, with both response rates and overall survival being influenced by distinct genetic features. These findings provide valuable insights into optimizing personalized treatment strategies for this challenging patient population.

摘要

目的

本研究旨在调查维奈克拉联合低甲基化药物(VEN + HMAs)治疗成年复发/难治性急性髓系白血病(R/R AML)患者后的疗效、反应及生存的临床和分子预测因素。

方法

我们回顾性分析了197例接受VEN + HMAs方案治疗的成年R/R AML患者。使用139个基因的靶向二代测序(NGS)进行分子谱分析,以探索潜在的反应和生存遗传预测因素。

结果

中位治疗周期为1(1 - 4)个周期。包括完全缓解(CR)和伴有血液学不完全恢复的CR(CRi)的综合完全缓解(CRc)率为44.7%,而总缓解率(ORR)达到59.9%。中位随访期为14.0个月(范围:0.7 - 54.0个月),1年和2年总生存率(OS)分别为55.4%和40.2%。多变量分析显示,[具体基因1]和[具体基因2]中的突变与更高的缓解率显著相关。相反,既往接受过HMA治疗、早期复发以及存在[具体基因3]突变与较低的缓解率相关。关于生存结果,[融合基因名称]融合基因以及[具体基因4]和[具体基因5]中的突变被发现是OS的有利预后因素,而[具体基因6]、[具体基因7]、[具体基因8]和[具体基因9]中的突变与较差的OS相关。

结论

VEN + HMAs方案在治疗R/R AML患者中显示出相当的疗效,缓解率和总生存率均受不同基因特征的影响。这些发现为优化这一具有挑战性患者群体的个性化治疗策略提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbb4/11852425/c3f5d4675d4d/cancers-17-00586-g001.jpg

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