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维利帕尼联合化疗治疗肺癌的疗效:系统评价与荟萃分析。

The efficacy of Veliparib in combination with chemotherapy in the treatment of lung cancer: systematic review and meta-analysis.

作者信息

Kashbour Muataz, Alhadeethi Abdulhameed, Awwad Sara, Yassin Mazen, Amin Ahmed, Abed Mohamed, Abdelmalik Abubaker, Alabdallat Yasmeen Jamal

机构信息

Diagnostic Radiology Department, National Cancer Institute, Misrata, Libya.

Medical Research Group of Egypt, Negida Academy, Arlington, Massachusetts, USA.

出版信息

Expert Rev Anticancer Ther. 2024 Dec;24(12):1237-1247. doi: 10.1080/14737140.2024.2417770. Epub 2024 Oct 20.

Abstract

OBJECTIVE

This meta-analysis aims to examine the effectiveness of veliparib, a poly ADP-ribose polymerase inhibitor, in combination with chemotherapy in treating bronchogenic carcinoma.

METHODS

PubMed, Cochrane, Scopus, and Web of Science were searched for eligible randomized controlled trials comparing veliparib plus chemotherapy to standard chemotherapy in adult lung cancer patients, until July 2023. The main outcomes were overall survival (OS) and progression-free survival (PFS).

RESULTS

This meta-analysis included six studies encompassing 2,136 patients. Veliparib has a slight OS improvement over placebo, HR = 0.91, 95% CI [0.83 to 1.0],  = 0.05. Veliparib offers more OS benefit in the subpopulation of non-small cell lung cancer (NSCLC) than small-cell lung cancer (SCLC), HR = 0.89, 95% CI [0.81,0.99],  = 0.03 and HR = 1.00, 95% CI [0.79, 1.28],  = 0.97, respectively. There was no significant PFS benefit between the two groups, HR = 0.92, 95% CI [0.81-1.01],  = 0.08).

CONCLUSION

Veliparib has a marginal inclination for overall survival improvement, more so in NSCLC, with an acceptable safety profile. Our results merit the pursuit of better-powered trials to support further the extent of veliparib's effectiveness in lung cancer patients.

REGISTRATION

PROSPERO (CRD42023453705).

摘要

目的

本荟萃分析旨在研究聚腺苷二磷酸核糖聚合酶抑制剂维利帕尼联合化疗治疗支气管源性癌的有效性。

方法

检索了PubMed、Cochrane、Scopus和Web of Science数据库,以查找比较维利帕尼联合化疗与标准化疗在成年肺癌患者中的合格随机对照试验,检索截至2023年7月。主要结局为总生存期(OS)和无进展生存期(PFS)。

结果

本荟萃分析纳入了6项研究,共2136例患者。维利帕尼与安慰剂相比,总生存期略有改善,HR = 0.91,95% CI [0.83至1.0],P = 0.05。在非小细胞肺癌(NSCLC)亚组中,维利帕尼的总生存期获益比小细胞肺癌(SCLC)更多,HR分别为0.89,95% CI [0.81,0.99],P = 0.03和HR = 1.00,95% CI [0.79,1.28],P = 0.97。两组之间无显著的无进展生存期获益,HR = 0.92,95% CI [0.81 - 1.01],P = 0.08。

结论

维利帕尼在改善总生存期方面有一定倾向,在NSCLC中更明显,且安全性可接受。我们的结果值得开展更具效力的试验,以进一步支持维利帕尼对肺癌患者的有效性程度。

注册信息

PROSPERO(CRD42023453705)

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