机构:[1]Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Pathology, Peking University Cancer Hospital & Institute, Beijing, China[2]Department of Pathology, West China Hospital, Sichuan University, Chengdu, Sichuan, China四川大学华西医院[3]Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China[4]Department of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, China[5]Zhongshan Hospital of Fudan University, Shanghai, China[6]Department of Pathology, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China[7]Zhejiang Cancer Hospital, Hangzhou, Zhejiang, China浙江省肿瘤医院[8]Nanjing Drum Tower Hospital, Nanjing, Jiangsu, China[9]Department of Pathology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China华中科技大学同济医学院附属同济医院[10]The first hospital of Jilin University - The Eastern Division, Changchun, Jilin, China[11]Medical Affairs Department, MSD China, Shanghai, China
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.
第一作者机构:[1]Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Pathology, Peking University Cancer Hospital & Institute, Beijing, China
共同第一作者:
通讯作者:
通讯机构:[1]Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Pathology, Peking University Cancer Hospital & Institute, Beijing, China[3]Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China[*1]Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Pathology, Peking University Cancer Hospital & Institute, Beijing, China[*2]Fudan University Cancer Hospital. 270 Dongan Road, Xuhui District, Shanghai, China
推荐引用方式(GB/T 7714):
Yang Xin,Jiang Lili,Jin Yan,et al.PD-L1 Expression in Chinese Patients with Advanced Non-Small Cell Lung Cancer (NSCLC): A Multi-Center Retrospective Observational Study[J].JOURNAL OF CANCER.2021,12(24):7390-7398.doi:10.7150/jca.63003.
APA:
Yang, Xin,Jiang, Lili,Jin, Yan,Li, Peng,Hou, Yingyong...&Lin, Dongmei.(2021).PD-L1 Expression in Chinese Patients with Advanced Non-Small Cell Lung Cancer (NSCLC): A Multi-Center Retrospective Observational Study.JOURNAL OF CANCER,12,(24)
MLA:
Yang, Xin,et al."PD-L1 Expression in Chinese Patients with Advanced Non-Small Cell Lung Cancer (NSCLC): A Multi-Center Retrospective Observational Study".JOURNAL OF CANCER 12..24(2021):7390-7398