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PD-1/PD-L1 抑制剂与化疗治疗晚期非小细胞肺癌的临床疗效和安全性分析:系统评价和荟萃分析。

Clinical Efficacy and Safety Analysis of PD-1/PD-L1 Inhibitor vs. Chemotherapy in the Treatment of Advanced Non-Small-Cell Lung Cancer: A Systematic Review and Meta-Analysis.

机构信息

Department of Respiratory and Critical Care Medicine, Taizhou First People's Hospital, Taizhou City, Zhejiang Province, China 318020.

出版信息

Biomed Res Int. 2022 Jun 25;2022:9500319. doi: 10.1155/2022/9500319. eCollection 2022.

Abstract

OBJECTIVE

To systematically evaluate the efficacy and safety of pembrolizumab (PD-1/PD-L inhibitor) and adjuvant chemotherapy to treat NSCLC and provide evidence-based reference for clinical use.

METHODS

By searching the Cochrane Library, EMBASE, PubMed, and Web of Science, according to the inclusion criteria, literature selection, data extraction, and quality evaluation were carried out for the included literature. The test was used to evaluate heterogeneity between studies, and the meta-analysis was performed using RevMan 5.3 software provided by Cochrane.

RESULTS

Finally, 14 relevant documents meeting the standards were included. It is a statistical difference in one-year survival rate [OR = 1.50, 95% CI (1.28, 1.76), < 0.00001, = 0%, = 4.99]; overall response rate[OR =1.57, 95% CI (1.29, 1.90), < 0.00001, = 0%, = 4.58]; progression-free survival [OR = 2.99, 95% CI (2.29, 3.91), < 0.00001, = 26%, = 8.00]; and overall survival [OR = 1.38, 95% CI (1.07, 1.78), = 0.01, = 46%, = 2.50] and reduces the incidence of adverse drug reactions [OR = 2.54, 95% CI (1.99, 3.25), < 0.00001, = 69%, = 7.43].

CONCLUSION

Pembrolizumab adjuvant chemotherapy is effective in the treatment of advanced NSCLC, but attention should be paid to the occurrence of adverse reactions in clinical. Due to the limitations of the methodology included in the study, this conclusion required more validation of large-sample RCT.

摘要

目的

系统评价派姆单抗(PD-1/PD-L 抑制剂)联合辅助化疗治疗 NSCLC 的疗效和安全性,为临床应用提供循证参考。

方法

通过检索 Cochrane 图书馆、EMBASE、PubMed 和 Web of Science,根据纳入标准,对纳入文献进行文献筛选、数据提取和质量评价。采用 检验评估研究间异质性,采用 Cochrane 提供的 RevMan 5.3 软件进行 Meta 分析。

结果

最终纳入符合标准的 14 篇相关文献。在一年生存率[OR = 1.50,95%CI(1.28,1.76), < 0.00001, = 0%, = 4.99]、总缓解率[OR = 1.57,95%CI(1.29,1.90), < 0.00001, = 0%, = 4.58]、无进展生存期[OR = 2.99,95%CI(2.29,3.91), < 0.00001, = 26%, = 8.00]和总生存期[OR = 1.38,95%CI(1.07,1.78), = 0.01, = 46%, = 2.50]方面均有统计学差异,且降低了药物不良反应的发生率[OR = 2.54,95%CI(1.99,3.25), < 0.00001, = 69%, = 7.43]。

结论

派姆单抗联合辅助化疗治疗晚期 NSCLC 有效,但临床应注意不良反应的发生。由于纳入研究的方法学存在局限性,这一结论需要更多大样本 RCT 的验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8386/9402310/12ba6cd47eab/BMRI2022-9500319.001.jpg

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