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A Network Meta-analysis Comparing the Efficacy and Safety of Anti-PD-1 with Anti-PD-L1 in Non-small Cell Lung Cancer.
You, Wei; Liu, Mei; Miao, Ji-Dong; Liao, Yu-Qian; Song, Yi-Bing; Cai, Dian-Kun; Gao, Yang; Peng, Hao.
  • You W; Department of Oncology, Zigong NO.4 People's Hospital, Zigong, Sichuan Province, 643000, People's Republic of China.
  • Liu M; Department of Oncology, Zigong NO.4 People's Hospital, Zigong, Sichuan Province, 643000, People's Republic of China.
  • Miao JD; Department of Oncology, Zigong NO.4 People's Hospital, Zigong, Sichuan Province, 643000, People's Republic of China.
  • Liao YQ; Department of Medical Oncology, Jiangxi Cancer Hospital, Nanchang, Jiangxi Province, 330029, People's Republic of China.
  • Song YB; Department of Oncology, Zigong NO.4 People's Hospital, Zigong, Sichuan Province, 643000, People's Republic of China.
  • Cai DK; Department of Oncology, Zigong NO.4 People's Hospital, Zigong, Sichuan Province, 643000, People's Republic of China.
  • Gao Y; Department of Oncology, Zigong NO.4 People's Hospital, Zigong, Sichuan Province, 643000, People's Republic of China.
  • Peng H; Department of Radiation Oncology, Sun Yat-sen University Cancer Center, People's Republic of China.
J Cancer ; 9(7): 1200-1206, 2018.
Article en En | MEDLINE | ID: mdl-29675101
ABSTRACT

Background:

This network meta-analysis aimed at comparing anti-programmed death 1 (anti-PD-1) with anti-programmed death ligand 1(anti-PD-L1) immunotherapy in patients with metastatic, previously treated non-small cell lung cancer (NSCLC) who failed first-line treatment.

Methods:

We searched electronic databases to identify all eligible clinical trials. End-points included overall survival (OS), progression-free survival (PFS) and objective response. Hazard ratios (HRs) or odds ratios (ORs) and corresponding 95% confidence intervals (CIs) were extracted. Network meta-analysis was performed using the frequentist approach for multiple treatment comparisons.

Results:

In total, 3024 patients were randomly assigned 1117 received anti-PD-1 therapy (nivolumab + pembrolizumab), 569 received anti-PD-L1 (atezolizumab) and 1338 received docetaxel. Anti-PD-1 (HR, 0.56; 95% CI, 0.48-0.66) and anti-PD-L1 (HR, 0.64; 95% CI, 0.51-0.79) achieved better OS than docetaxel, and anti-PD-1 was superior to docetaxel in terms of PFS (HR, 0.75; 95% CI, 0.62-0.89). Moreover, anti-PD-1 achieved the highest effect on OS and PFS, with a P-score of 91.2% and 95.5%, respectively. With regard to tumor response, anti-PD-1 group had a higher rate of responders than that in anti-PD-L1 (HR, 0.35; 95% CI, 0.19-0.65) and docetaxel (HR, 0.36; 95% CI, 0.25-0.52) groups. Undoubtedly, anti-PD-1 and anti-PD-L1 obtained less toxicity profile than docetaxel, and no significant difference was observed between anti-PD-1 and anti-PD-L1 groups.

Conclusions:

Anti-PD-1 may be a better choice for patients with metastatic and previously treated NSCLC who failed first-line treatment in terms of the treatment ranking.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Systematic_reviews Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Systematic_reviews Idioma: En Año: 2018 Tipo del documento: Article