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评估聚(ADP-核糖)聚合酶(PARP)抑制剂用于晚期肺癌治疗的获益和安全性概况:一项全面的系统评价和荟萃分析。

Assessing the benefits and safety profile of incorporating poly ADP-ribose polymerase (PARP) inhibitors in the treatment of advanced lung cancer: a thorough systematic review and meta-analysis.

作者信息

Tang Min, Wang Yue, Li Pulin, Han Rui, Wang Ran

机构信息

Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Anhui Medical University, Hefei, China.

Department of Infectious Disease, Hefei Second People's Hospital, Hefei, China.

出版信息

Front Pharmacol. 2024 Jun 21;15:1338442. doi: 10.3389/fphar.2024.1338442. eCollection 2024.

Abstract

BACKGROUND

Poly (ADP-Ribose) Polymerase (PARP) inhibitors represent a novel class of drugs that hinder DNA repair mechanisms in tumor cells, leading to cell death. This systematic review aims to evaluate the effectiveness, safety, and potential adverse effects of PARP inhibitors (PARPi) in the management of patients with advanced lung cancer.

MATERIALS AND METHODS

We conducted a comprehensive search for relevant studies in PubMed, Embase, Cochrane, and ClinicalTrials.gov. We extracted primary and secondary outcome measures, including progression-free survival (PFS), overall survival (OS), and adverse events (AEs), from the identified literature for subsequent meta-analysis and systematic review.

RESULTS

This study encompassed twelve randomized controlled trials, involving 3,132 patients with advanced lung cancer. In comparison to non-PARPi treatments, the administration of PARPi significantly extended OS (hazard ratio (HR) = 0.90, 95% CI = 0.83-0.97, = 0.006). However, the difference in PFS did not reach statistical significance.

CONCLUSION

In summary, therapies incorporating PARPi provide a degree of benefit by extending OS in patients with advanced lung cancer. Nonetheless, further trials are necessary to furnish additional evidence regarding the efficacy and safety of PARPi in the treatment of lung cancer.

UNLABELLED

https://www.crd.york.ac.uk/PROSPERO/, identifier number: CRD42023424673.

摘要

背景

聚(ADP - 核糖)聚合酶(PARP)抑制剂是一类新型药物,可阻碍肿瘤细胞中的DNA修复机制,导致细胞死亡。本系统评价旨在评估PARP抑制剂(PARPi)在晚期肺癌患者管理中的有效性、安全性和潜在不良反应。

材料与方法

我们在PubMed、Embase、Cochrane和ClinicalTrials.gov中全面检索了相关研究。我们从已识别的文献中提取了主要和次要结局指标,包括无进展生存期(PFS)、总生存期(OS)和不良事件(AE),用于后续的荟萃分析和系统评价。

结果

本研究纳入了12项随机对照试验,涉及3132例晚期肺癌患者。与非PARPi治疗相比,PARPi的使用显著延长了总生存期(风险比(HR)= 0.90,95%置信区间 = 0.83 - 0.97,P = 0.006)。然而,无进展生存期的差异未达到统计学意义。

结论

总之,含PARPi的治疗方法通过延长晚期肺癌患者的总生存期提供了一定程度的益处。尽管如此,仍需要进一步的试验来提供关于PARPi治疗肺癌有效性和安全性的更多证据。

未标注

https://www.crd.york.ac.uk/PROSPERO/,标识符编号:CRD42023424673。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d56b/11234112/3d9f22fa1ed2/fphar-15-1338442-g001.jpg

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