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

被引:0
|
作者
Roussos, Petros [1 ]
Migkou, Magdalini [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Alexandra Hosp, Med Sch, Therapeut Clin, Leof Vasilissis Sofias 80, Athens 11528, Greece
来源
CANCER PATHOGENESIS AND THERAPY | 2024年 / 2卷 / 03期
关键词
Non-small cell lung cancer; PD-1; inhibitors; PD-L1; Immunotherapy; Systematic review; METASTATIC NONSQUAMOUS NSCLC; 1ST-LINE TREATMENT; PHASE-3; CHEMOTHERAPY; GEMCITABINE; PLATINUM; BLIND;
D O I
10.1016/j.cpt.2023.09.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 PD1/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.
引用
收藏
页码:155 / 163
页数:9
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