| Literature DB >> 32635291 |
Jorge García-González1, Juan Ruiz-Bañobre1, Francisco J Afonso-Afonso2, Margarita Amenedo-Gancedo3, María Del Carmen Areses-Manrique4, Begoña Campos-Balea5, Joaquín Casal-Rubio6, Natalia Fernández-Núñez5, José Luis Fírvida Pérez4, Martín Lázaro-Quintela6, Diego Pérez Parente7, Leonardo Crama7, Pedro Ruiz-Gracia7, Lucía Santomé-Couto8, Luis León-Mateos1.
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, p < 0.001) and overall survival (OS) (HR = 0.76, 95% CI: 0.67-0.86; p < 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, p < 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.Entities:
Keywords: PD-1 inhibitors; PD-L1 inhibitors; chemotherapy; immunotherapy; meta-analysis; non-small-cell lung cancer
Year: 2020 PMID: 32635291 DOI: 10.3390/jcm9072093
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241