The prognostic value of PD-L1 expression for non-small cell lung cancer patients: a meta-analysis

Eur J Surg Oncol. 2015 Apr;41(4):450-6. doi: 10.1016/j.ejso.2015.01.020. Epub 2015 Jan 31.

Abstract

Background: A meta-analysis was conducted to investigate the much-debated relationship between the gene expression of programmed cell death-ligand 1 (PD-L1) and cancer patient prognosis. The prognostic value of measuring PD-L1 expression in non-small cell lung cancer (NSCLC) patients was analyzed.

Methods: We searched PubMed for studies about the relationship between PD-L1 expression and NSCLC patient prognosis. Only studies with patient survival data related to PD-L1 expression in NSCLC patients with different characteristics were included. The effect size (ES) for this analysis was the hazard ratio (HR) with 95% confidence intervals (CI) for overall survival (OS).

Results: Six studies with 1157 patients were included with the defined including and excluding criteria. There is no significant heterogeneity among the studies (I(2) = 0%, p = 0.683). PD-L1 expression was significantly associated with the differentiation of tumor (poor vs. well: OR = 1.91, 95% CI: 1.33-2.75, p = 0.001). High PD-L1 expression was also correlated with poor prognosis in terms of the OS of patients with NSCLC (pooled HR = 1.75, 95% CI: 140-2.20, p < 0.001; heterogeneity test: I(2) = 0%, p = 0.643).

Conclusions: NSCLC patients with positive PD-L1 expression exhibited poor OS. The PD-L1 expression was higher in tumors with poor differentiation.

Keywords: Differentiation; NSCLC; Overall survival; Prognostic; Programmed cell death-ligand 1.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • B7-H1 Antigen / genetics*
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Carcinoma, Non-Small-Cell Lung / pathology*
  • Gene Expression*
  • Humans
  • Lung Neoplasms / genetics*
  • Lung Neoplasms / pathology*
  • Neoplasm Grading
  • Predictive Value of Tests
  • Prognosis
  • Survival Rate

Substances

  • B7-H1 Antigen
  • CD274 protein, human