Association between PD-L1 Expression on Tumour-Infiltrating Lymphocytes and Overall Survival in Patients with Gastric Cancer

被引:27
作者
Fang, Wenfeng [1 ,2 ,3 ]
Chen, Ying [4 ]
Sheng, Jin [1 ,2 ,3 ]
Zhou, Ting [1 ,2 ,3 ]
Zhang, Yaxiong [1 ,2 ,3 ]
Zhan, Jianhua [1 ,2 ,3 ]
Liu, Lin [4 ]
Huang, Jiaxing [4 ]
Peng, Peijian [4 ]
Zhang, Li [1 ,2 ,3 ]
机构
[1] Sun Yat Sen Univ, Dept Med Oncol, Canc Ctr, 651 Dongfeng Rd East, Guangzhou 510060, Guangdong, Peoples R China
[2] State Key Lab Oncol South China, Guangzhou, Guangdong, Peoples R China
[3] Collaborat Innovat Ctr Canc Med, Guangzhou, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 5, Dept Med Oncol, 52 Mei Hua Rd East, Zhu Hai 519000, Guangdong, Peoples R China
关键词
gastric cancer; PD-L1; TILs; DEATH-LIGAND; 1; CELL LUNG-CANCER; PROGNOSTIC-SIGNIFICANCE; ANTI-PD-L1; ANTIBODY; CARCINOMA; SAFETY; B7-H1;
D O I
10.7150/jca.18729
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Targeting of the PD-1/PD-L1 signalling pathway is a promising treatment strategy in several cancers. The aim of this study was to assess the expression of PD-L1 on tumour cells and tumour-infiltrating lymphocytes (TILs) in gastric cancer (GC) and its prognostic impact. Materials and Methods A total of 240 patients who were diagnosed with GC at Sun Yat-sen University Cancer Centre (SYSUCC) from May 2008 to December 2013 were included in this study. PD-L1 expression was detected by immunohistochemistry (IHC) in all GC tumour specimens. The Cox proportional hazard regression model was used to assess the association between PD-L1 expression and overall survival (OS). Results The positive rates of PD-L1 expression on tumour cells and TILs were 74.8% and 65.8%, respectively. Patients with poor tumour differentiation had higher positive rates of PD-L1 expression on tumour cells (p=0.023). There was no significant association between PD-L1 expression on tumour cells and other clinicopathological data. In TILs, PD-L1 expression was significantly higher in patients who underwent surgery (p=0.031) and were in the late stage (p=0.021) than those without surgery and in the early stage. Patients with positive PD-L1 expression on TILs had a significantly shorter five-year OS than those with negative PD-L1 expression (14.2 vs 18.3; p=0.001); therefore, PD-L1 expression on TILs is an independent prognostic factor. However, PD-L1 expression on tumour cells is not associated with OS (p=0.945). Conclusion Our findings suggest that PD-L1 expression on TILs may be a predictive factor for immunotherapy of PD-1/PD-L1 pathway inhibitors.
引用
收藏
页码:1579 / 1585
页数:7
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