PD-1/PD-L1 抑制剂对 III 期非小细胞肺癌患者生存期的影响:系统综述

Petros Roussos, Magdalini Migkou
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引用次数: 0

摘要

背景肺癌是癌症相关死亡的主要原因,而非小细胞肺癌(NSCLC)是其主要亚型。程序性死亡1(PD-1)和程序性死亡配体1(PD-L1)抑制剂被广泛用于治疗IV期NSCLC。本研究系统回顾了相关文献,以明确PD-1/PD-L1抑制剂治疗对III期NSCLC患者生存期的影响。方法对2012年11月至2022年11月期间发表的、以英文撰写的、对III期NSCLC患者使用PD-1/PD-L1抑制剂的随机III期临床试验进行回顾。信息来源包括MEDLINE数据库(最后查询日期为2022年12月26日)、ScienceDirect网站(最后查询日期为2022年12月26日)和CENTRAL注册表(最后查询日期为2022年12月27日)。研究结果包括总生存期(OS)、无进展生存期(PFS)、无疾病生存期(DFS)和无事件生存期(EFS)。偏倚风险评估根据《科克伦干预措施系统综述手册》5.1.0 版进行。根据推荐、评估、发展和评价分级(GRADE)指南对研究结果的确定性进行了评估。对参与者进行分组的主要特征是疾病组织学、癌细胞中PD-L1表达的百分比和治疗时间。OS和PFS均有所改善(风险比[RR]:0.85;95% 置信区间 [CI]:在化疗后使用 PD-L1 抑制剂可改善 OS 和 PFS(风险比 [RR]:0.85;95% 置信区间 [CI]:0.75-0.96 和 RR:0.75;95% CI:0.70-0.86,分别为 0.75 和 0.86),在非鳞癌 NSCLC 中使用一线 PD-1 抑制剂加化疗可改善 OS(RR:0.40;95% CI:0.17-0.95)。结论本综述强调了PD-L1抑制剂在化疗后用于III期NSCLC的OS和PFS获益,以及一线PD-1抑制剂加化疗用于非鳞癌III期疾病的OS获益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Impact of PD-1/PD-L1 inhibitors on survival in stage III non-small-cell lung cancer: A systematic review

Impact of PD-1/PD-L1 inhibitors on survival in stage III non-small-cell lung cancer: A systematic review

Background

Lung cancer is the leading cause of cancer-related death, and non-small-cell lung cancer (NSCLC) is the predominant subtype. Programmed death 1 (PD-1) and programmed death-ligand 1 (PD-L1) inhibitors are widely used to treat stage IV NSCLC. This study systematically reviewed the literature to clarify the impact of PD-1/PD-L1 inhibitor treatment on the survival of patients with stage III NSCLC.

Methods

Randomized phase III clinical trials of PD-1/PD-L1 inhibitors administered to patients with stage III NSCLC that were written in English and published between November 2012 and November 2022 were eligible for review. The sources of information were the MEDLINE database (last consulted on December 26, 2022), ScienceDirect website (last consulted on December 26, 2022), and CENTRAL register (last consulted on December 27, 2022). The outcomes of interest were overall survival (OS), progression-free survival (PFS), disease-free survival (DFS), and event-free survival (EFS). Risk of bias assessments were performed according to the Cochrane Handbook for Systematic Reviews of Interventions version 5.1.0. The findings have been assessed for certainty according to the Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) guidelines.

Results

Fourteen eligible studies and 2788 participants were included in the review. The key characteristics used to group the participants were disease histology, percentage of PD-L1 expression in cancer cells, and timeline of therapy. OS and PFS were improved (risk ratio [RR]: 0.85; 95% confidence interval [CI]: 0.75–0.96 and RR: 0.75; 95% CI: 0.70–0.86, respectively) based on the use of PD-L1 inhibitors after chemoradiation and OS was improved using first-line PD-1 inhibitors plus chemotherapy in non-squamous NSCLC (RR: 0.40; 95% CI: 0.17–0.95), with the GRADE results indicating moderate quality of evidence.

Conclusion

This review highlights the OS and PFS benefits of PD-L1 inhibitors in stage III NSCLC when used after chemoradiation and OS benefits of first-line PD-1 inhibitors added to chemotherapy in non-squamous stage III disease.

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来源期刊
Cancer pathogenesis and therapy
Cancer pathogenesis and therapy Surgery, Radiology and Imaging, Cancer Research, Oncology
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