PD-L1 expression in lung cancer and its correlation with driver mutations: a meta-analysis

被引:165
|
作者
Zhang, Minghui [1 ]
Li, Guoliang [2 ]
Wang, Yanbo [3 ]
Yan Wang [4 ]
Shu Zhao [1 ]
Pu Haihong [1 ]
Zhao, Hongli [1 ]
Wang, Yan [1 ]
机构
[1] Harbin Med Univ, Canc Hosp, Dept Med Oncol, Harbin 150081, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 2, Dept Gen Surg, Harbin 150040, Heilongjiang, Peoples R China
[3] Harbin Med Univ, Canc Hosp, Dept Surg Oncol, Harbin 150081, Heilongjiang, Peoples R China
[4] Heilongjiang Prov Hosp, Dept Med Oncol, Harbin 150030, Heilongjiang, Peoples R China
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
DEATH-LIGAND; 1; INFILTRATING T-CELLS; POOR-PROGNOSIS; EGFR; ASSOCIATION; CARCINOMA; SURVIVAL; ADENOCARCINOMA; STATISTICS; OVEREXPRESSION;
D O I
10.1038/s41598-017-10925-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although many studies have addressed the prognostic value of programmed cell death-ligand 1 (PDL1) expression in lung cancer, the results remain controversial. A systematic search of the PubMed, EMBASE, and Cochrane Library databases was performed to identify the correlation between PD-L1 expression and driver mutations and overall survival (OS). This meta-analysis enrolled a total of 11,444 patients for 47 studies, and the pooled results showed that increased PD-L1 expression was associated with poor prognosis (HR = 1.40, 95% CI: 1.19-1.65, P < 0.001). In subgroup analysis stratified according to histology types, the pooled results demonstrated that increased PD-L1 expression was an unfavorable prognostic factor for non-small cell lung cancer (NSCLC) (HR = 1.26, 95% CI: 1.05-1.52, P = 0.01) and pulmonary lymphoepithelioma-like carcinoma (LELC) (HR = 3.04, 95% CI: 1.19-7.77, P = 0.02), rather than small cell lung cancer (SCLC) (HR = 0.62, 95% CI: 0.27-1.39, P = 0.24). The pooled ORs indicated that PD-L1 expression was associated with gender, smoking status, histology, differentiation, tumour size, lymph nodal metastasis, TNM stage and EGFR mutation. However, PD-L1 expression was not correlated with ALK rearrangement and KRAS mutations.
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页数:10
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