Classifying Non-Small Cell Lung Cancer by Status of Programmed Cell Death Ligand 1 and Tumor-Infiltrating Lymphocytes on Tumor Cells

被引:14
作者
Cui, Shaohua [1 ]
Dong, Lili [1 ]
Qian, Jialin [1 ]
Ye, Lin [1 ]
Jiang, Liyan [1 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Resp Med, Shanghai Chest Hosp, 241 HuaiHai W Rd, Shanghai 200030, Peoples R China
关键词
Programmed death ligand 1 (PD-L1); tumor-infiltrating lymphocytes (TIL); non-small cell lung cancer (NSCLC); immunotherapy; NIVOLUMAB; DOCETAXEL; ANTIBODY; SAFETY; PD-L1;
D O I
10.7150/jca.21842
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To explore the possible correlation between programmed death ligand 1 (PD-L1)/tumor-infiltrating lymphocytes (TIL) status and clinical factors in non-small cell lung (NSCLC). Materials and Methods: A total of 126 surgical NSCLC samples with stage I to IIIA were retrospectively collected and analyzed. Immunohistochemistry (IHC) assays were used to detect PD-L1 protein expression. PD-L1 positivity on tumor cells was defined by positive tumor cell (TC) percentage using 5% cutoff value. Results: Thirty-seven patients (29.4%), thirty patients (23.8%), six patients (4.8%) and fifty-three patients (42%) were classified as type I (PD-L1+, TIL+), type II (PD-L1-, TIL-), type III (PD-L1+, TIL-) and type IV (PD-L1-, TIL+) tumor environments according to PD-L1/TIL status, respectively. Statistical differences could be observed in factors including gender (P<0.001), smoking status (P<0.001), age (P=0.002), histological types (P<0.001), EGFR mutation (P=0.008) and KRAS mutation (P=0.003) across the four type tumors. Type I tumors were associated with ever smoking, non-adenocarcinoma histological types and KRAS mutation. Type II tumors were associated with female gender, never-smoking, adenocarcinoma histological types and EGFR mutation. Type III tumors were associated with ever smoking and type IV tumors were associated with female gender and EGFR mutation. Conclusion: Clinical factors associated with NSCLC microenvironment types based on PD-L1/TIL differed a lot across different types. The findings of this study may help to facilitate the understanding of the relationship between tumor microenvironment and clinical factors, and also the selecting of patients for combination immunotherapies.
引用
收藏
页码:129 / 134
页数:6
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