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On the way of the new strategies aimed to improve the efficacy of PD-1/PD-L1 immune checkpoint blocking mAbs in small cell lung cancer
- Source :
- Transl Lung Cancer Res
- Publication Year :
- 2020
-
Abstract
- BACKGROUND: This study aimed to characterize programmed death ligand-1 (PD-L1) expression and CD8(+) tumor-infiltrating lymphocytes (TILs) density, and their impact on survival in patients with surgically resected small-cell lung cancer (SCLC). METHODS: Fifty-six patients with surgically resected SCLC were included. PD-L1 protein expression and CD8(+) TILs were tested by immunohistochemistry. A meta-analysis of 15 articles with 1,505 patients that investigated the prevalence and prognostic significance of PD-L1 expression in SCLC was conducted. RESULTS: Twenty-two (39.3%) patients had positive PD-L1 protein expression and 42 (75.0%) had high CD8(+) TILs density. PD-L1 expression level was not associated with CD8(+) TILs density (P=0.528). No any association between clinicopathological features and PD-L1 expression level or CD8(+) TILs density was observed. Positive PD-L1 expression [hazard ratio (HR) =0.374, P=0.002] and high CD8(+) TILs density (HR =0.429, P=0.008) were independently associated with significantly longer overall survival (OS), which remain the statistical significance in multivariate analyses (P=0.007, P=0.002; respectively). Meta-analysis showed that the prevalence of positive PD-L1 expression was 0.35 [95% confidence interval (CI), 0.22–0.48] and positive PD-L1 expression was correlated with markedly longer OS (HR =0.61; 95% CI, 0.31–0.91) in patients with SCLC. CONCLUSIONS: The prevalence of PD-L1 expression in surgically resected SCLC is lower than that published for NSCLC. There was no association between PD-L1 expression or CD8(+) TILs density and clinicopathological parameters. PD-L1 expression and CD8(+) TILs density was independently correlated with better outcome in patients with SCLC.
Details
- ISSN :
- 22186751
- Volume :
- 9
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Translational lung cancer research
- Accession number :
- edsair.doi.dedup.....d6d61e42c4f69bb40f5fe01363b97cb8