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

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单位: [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
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关键词: non-small cell lung cancer programmed death-ligand 1 immunohistochemistry driver mutations

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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.

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出版当年[2020]版:
大类 | 3 区 医学
小类 | 3 区 肿瘤学
最新[2025]版:
大类 | 3 区 医学
小类 | 4 区 肿瘤学
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出版当年[2019]版:
Q2 ONCOLOGY
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Q2 ONCOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2019版] 出版当年五年平均 出版前一年[2018版] 出版后一年[2020版]

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第一作者单位: [1]Peking Univ, Canc Hosp & Inst, Dept Pathol, Key Lab Carcinogenesis & Translat Res,Minist Educ, Beijing, Peoples R China
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通讯机构: [3]Fudan Univ, Shanghai Canc Ctr, Dept Pathol, Shanghai, Peoples R China [*1]Fudan Univ, Canc Hosp, 270 Dongan Rd, Shanghai, Peoples R China
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