Prognostic value of PD -L1 expression in patients with primary solid tumors

Xiao Xiang(Tumor Hospital of Guangxi Medical University), Pengcheng Yu(Guangxi Medical University), Di Long(Guangxi Medical University), Xiao-Li Liao(Tumor Hospital of Guangxi Medical University), Sen Zhang(Guangxi Medical University), Xue‐Mei You(Tumor Hospital of Guangxi Medical University), Jian‐Hong Zhong(Tumor Hospital of Guangxi Medical University), Lequn Li(Tumor Hospital of Guangxi Medical University)
Oncotarget
December 22, 2017
Cited by 61Open Access
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Abstract

Programmed death-ligand 1 (PD-L1) is thought to play a critical role in immune escape by cancer, but whether PD-L1 expression can influence prognosis of patients with solid tumors is controversial. Therefore, we meta-analyzed available data on whether PD-L1 expression correlates with overall survival (OS) in such patients. PubMed, EMBASE and other databases were systematically searched for cohort or case-control studies examining the possible correlation between PD-L1 expression and OS of patients with solid tumors. OS was compared between patients positive or negative for PD-L1 expression using scatter plots, and subgroup analyses were performed based on tumor type and patient characteristics. Data from 59 studies involving 20,004 patients with solid tumors were meta-analyzed. The median percentage of tumors positive for PD-L1 was 30.1%. OS was significantly lower in PD-L1-positive patients than in PD-L1-negative patients at 1 year (P = 0.039), 3 years (P < 0.001) and 5 years (P < 0.001). The risk ratios of OS (and associated 95% confidence intervals) were 2.02 (1.56-2.60) at 1 year, 1.57 (1.34-1.83) at 3 years and 1.43 (1.24-1.64) at 5 years. Similar results were obtained in subgroup analyses based on patient ethnicity or tumor type. The available evidence suggests that PD-L1 expression negatively affects the prognosis of patients with solid tumors. PD-L1 might serve as an efficient prognostic indicator in solid tumor and may represent the important new therapeutic target.


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