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程序性死亡受体 1(PD-1)/程序性死亡配体 1(PD-L1)抑制剂联合化疗作为非小细胞肺癌一线治疗的成对荟萃分析

PD-(L)1 Inhibitors in Combination with Chemotherapy as First-Line Treatment for Non-Small-Cell Lung Cancer: A Pairwise Meta-Analysis.

作者信息

García-González Jorge, Ruiz-Bañobre Juan, Afonso-Afonso Francisco J, Amenedo-Gancedo Margarita, Areses-Manrique María Del Carmen, Campos-Balea Begoña, Casal-Rubio Joaquín, Fernández-Núñez Natalia, Fírvida Pérez José Luis, Lázaro-Quintela Martín, Pérez Parente Diego, Crama Leonardo, Ruiz-Gracia Pedro, Santomé-Couto Lucía, León-Mateos Luis

机构信息

Medical Oncology Department, University Clinical Hospital of Santiago de Compostela and Translational Medical Oncology Group (Oncomet), Health Research Institute of Santiago de Compostela (IDIS), CIBERONC, 15706 Santiago de Compostela, Spain.

Medical Oncology Department, Complexo Hospitalario Universitario de Ferrol, 15405 A Coruña, Spain.

出版信息

J Clin Med. 2020 Jul 3;9(7):2093. doi: 10.3390/jcm9072093.

Abstract

The combination of programmed cell death-1 (PD-1)/programmed death ligand-1 (PD-L1) inhibitors with chemotherapy has emerged as a promising therapeutic option for advanced non-small-cell lung cancer (NSCLC). The aim of this meta-analysis was to evaluate the efficacy of the combined strategy in this setting. For this purpose, we performed a literature search of randomized controlled trials comparing PD-(L)1 inhibitors plus platinum-based chemotherapy versus chemotherapy alone in stage IV NSCLC patients. Seven clinical trials with 4562 patients were included. In the intention-to-treat wildtype population, PD-(L)1 inhibitor plus chemotherapy was significantly associated with improved progression-free survival (PFS) (Hazard ratio (HR) = 0.61, 95% confidence interval (CI): 0.57-0.65, < 0.001) and overall survival (OS) (HR = 0.76, 95% CI: 0.67-0.86; < 0.001) compared to chemotherapy. A significantly higher overall response rate (ORR) was also observed with the combined strategy (Odds ratio (OR) = 2.12, 95% CI: 1.70-2.63, < 0.001). Furthermore, in all the analyzed subgroups, addition of PD-(L)1 inhibitors to chemotherapy significantly improved efficacy endpoints. Specifically, stratification according to PD-L1 expression revealed a benefit across all patients, regardless of their PFS status. In conclusion, PD-(L)1 blockade added to standard platinum-based chemotherapy significantly improved PFS, OS, and ORR in the up-front treatment of advanced NSCLC.

摘要

程序性细胞死亡蛋白1(PD-1)/程序性死亡配体1(PD-L1)抑制剂与化疗联合使用,已成为晚期非小细胞肺癌(NSCLC)一种很有前景的治疗选择。本荟萃分析的目的是评估这种联合策略在该情况下的疗效。为此,我们对比较PD-(L)1抑制剂加铂类化疗与单纯化疗用于IV期NSCLC患者的随机对照试验进行了文献检索。纳入了7项临床试验,共4562例患者。在意向性治疗野生型人群中,与化疗相比,PD-(L)1抑制剂加化疗与无进展生存期(PFS)改善显著相关(风险比(HR)=0.61,95%置信区间(CI):0.57-0.65,P<0.001)和总生存期(OS)(HR = 0.76,95% CI:0.67-0.86;P<0.001)。联合策略还观察到显著更高的总缓解率(ORR)(优势比(OR)=2.12,95% CI:1.70-2.63,P<0.001)。此外,在所有分析的亚组中,化疗中添加PD-(L)1抑制剂均显著改善了疗效终点。具体而言,根据PD-L1表达进行分层显示,所有患者均有获益,无论其PFS状态如何。总之,在晚期NSCLC的一线治疗中,在标准铂类化疗基础上加用PD-(L)1阻断剂可显著改善PFS、OS和ORR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2714/7408884/fb4d7050603d/jcm-09-02093-g001.jpg

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