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Correlation Study on Expression of PD-1 and PD-L1 in Non-small Cell Lung Cancer and Epidermal Growth Factor Receptor Mutations

Authors :
Ling JIANG
Zhiyi LIN
Na LI
Jinfang JIANG
Cengceng LU
Shenghang DU
Jun ZHANG
Yuanyuan WANG
Jun CHEN
Ping GONG
Source :
Chinese Journal of Lung Cancer, Vol 24, Iss 9, Pp 623-631 (2021)
Publication Year :
2021
Publisher :
Chinese Anti-Cancer Association; Chinese Antituberculosis Association, 2021.

Abstract

Background and objective The treatment mode of lung cancer is epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) as a first-line treatment for patients with EGFR mutant in non-small cell lung cancer (NSCLC). At the same time programmed death receptor 1 (PD-1) and its programmed death receptor ligand 1 (PD-L1) inhibitors therapy as the representative immune checkpoint inhibitors (ICIs) has a significant effect in the treatment of lung cancer. The aim of this study was to investigate the correlation between the expression of PD-1 and PD-L1 in NSCLC and clinicopathologic feature, EGFR gene mutation. Methods The protein expression of PD-1 and PD-L1 was detected by immunohistochemistry from 127 patients with NSCLC and EGFR gene mutation was detected by quantitative polymerase chain reaction (qPCR) to analyze its relation with clinicopathologic feature. Also, the correlation between protein expression of PD-1 and PD-L1 and EGFR mutation. Results The PD-1 positive expression in NSCLC tumor cells and tumor infiltrating immune cells is 53.5% (68/127), PD-L1 is 57.5% (73/127). The PD-1 and PD-L1 expression significantly higher in well-differentiated and moderately-differentiated carcinoma than poorly differentiated carcinoma, I+II than III+IV in clinical staging (P

Details

Language :
Chinese
ISSN :
10093419 and 19996187
Volume :
24
Issue :
9
Database :
Directory of Open Access Journals
Journal :
Chinese Journal of Lung Cancer
Publication Type :
Academic Journal
Accession number :
edsdoj.5aeb5f855edd4f04b5f137df9b83e308
Document Type :
article
Full Text :
https://doi.org/10.3779/j.issn.1009-3419.2021.102.31