PD-L1 Expression in Chinese Patients with Advanced Non-Small Cell Lung Cancer (NSCLC): A Multi-Center Retrospective Observational Study

被引:16
|
作者
Yang, Xin [1 ]
Jiang, Lili [2 ]
Jin, Yan [3 ]
Li, Peng [4 ]
Hou, Yingyong [5 ]
Yun, Jingping [4 ]
Wu, Chunyan [6 ]
Sun, Wenyong [7 ]
Fan, Xiangshan [8 ]
Kuang, Dong [9 ]
Wang, Weiya [2 ]
Ni, Jinsong [10 ]
Mao, Anhua [11 ]
Tang, Wenmin [11 ]
Liu, Zhenhua [11 ]
Wang, Jiali [11 ]
Xiao, Suijun [11 ]
Li, Yuan [3 ]
Lin, Dongmei [1 ]
机构
[1] Peking Univ, Canc Hosp & Inst, Dept Pathol, Key Lab Carcinogenesis & Translat Res,Minist Educ, Beijing, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Pathol, Chengdu, Sichuan, Peoples R China
[3] Fudan Univ, Shanghai Canc Ctr, Dept Pathol, Shanghai, Peoples R China
[4] Sun Yat Sen Univ, Canc Ctr, Dept Pathol, Guangzhou, Peoples R China
[5] Fudan Univ, Zhongshan Hosp, Shanghai, Peoples R China
[6] Tongji Univ, Shanghai Pulm Hosp, Sch Med, Dept Pathol, Shanghai, Peoples R China
[7] Zhejiang Canc Hosp, Hangzhou, Zhejiang, Peoples R China
[8] Nanjing Drum Tower Hosp, Nanjing, Jiangsu, Peoples R China
[9] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Pathol, Wuhan, Hubei, Peoples R China
[10] First Hosp Jilin Univ, Eastern Div, Changchun, Jilin, Peoples R China
[11] MSD China, Med Affairs Dept, Shanghai, Peoples R China
来源
JOURNAL OF CANCER | 2021年 / 12卷 / 24期
关键词
non-small cell lung cancer; programmed death-ligand 1; immunohistochemistry; driver mutations; OPEN-LABEL; BRAIN METASTASES; REAL-WORLD; PEMBROLIZUMAB; PREVALENCE; SURVIVAL;
D O I
10.7150/jca.63003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: This study aimed to investigate the prevalence of tumor programmed death-ligand 1 (PD-L1) expression in Chinese patients with advanced Non-Small Cell Lung Cancer (NSCLC). Methods: Tumor tissues with histologically confirmed stage IIIB/IV NSCLC were retrospectively obtained from 10 centers in China. PD-L1 expression was determined using the PD-L1 IHC 22C3 pharmDx kit (Agilent, Santa Clara, CA, USA) and the samples were repetitively assayed with the PD-L1 IHC 22C3 Ab concentrate (Agilent, Santa Clara, CA, USA). Results: Out of 901 patients who met the inclusion criteria, 879 (97.6%) had evaluable PD-L1 data. The number of patients with a PD-L1 tumor proportion score (TPS) < 1%, 1-49%, and >= 50% (corresponding to PD-L1 non-expression, low expression, and high expression) was 424 (48.2%), 266 (30.3%), and 189 (21.5%), respectively. PD-L1 expression was more likely to be found in patients younger than 75 years, men, current or former smokers, those with good performance status (PS) scores, and those with a wild-type epidermal growth factor receptor (EGFR). PD-L1 TPS >= 50% and >= 1% were respectively 28.0% and 50.2% among patients negative for both EGFR mutation and anaplastic lymphoma kinase (ALK) rearrangement. PD-L1 expression determined using the 22C3 antibody concentrate and pharmDx kit had comparable results. Conclusions: The prevalence of PD-L1 expression in advanced NSCLC was consistent with that reported in the global EXPRESS study. Age, gender, smoking history, PS scores, and EGFR/ALK mutation status affected PD-L1 expression. The 22C3 antibody concentrate appears to be an alternative reagent for the PD-L1 assay.
引用
收藏
页码:7390 / 7398
页数:9
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