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  4. PD-L1 expression and outcome in patients with metastatic non-small cell lung cancer and EGFR mutations receiving EGFR-TKI as frontline treatment
 
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PD-L1 expression and outcome in patients with metastatic non-small cell lung cancer and EGFR mutations receiving EGFR-TKI as frontline treatment

Journal
OncoTargets and Therapy
Journal Volume
14
Pages
2301-2309
Date Issued
2021
Author(s)
Chang C.-Y.
Lai Y.-C.
Wei Y.-F.
CHUNG-YU CHEN  
Chang S.-C.
DOI
10.2147/OTT.S290445
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85104100933&doi=10.2147%2fOTT.S290445&partnerID=40&md5=3b90cbd602c5d259f0b7df8cead039a9
https://scholars.lib.ntu.edu.tw/handle/123456789/579171
Abstract
Background: Epidermal growth factor receptor (EGFR) mutations are most common in Eastern Asia, and frequencies of 30-50% have been reported. EGFR-tyrosine kinase inhibitors (TKIs) are recommended as first-line therapeutic options for non-small cell lung cancer (NSCLC) with sensitizing EGFR mutations. Several immune checkpoint inhibitors have been successful in improving the outcomes of advanced lung cancer. The expression of programmed cell death-ligand 1 (PD-L1) on tumor cells plays an important role in predicting the efficacy of programmed cell death protein 1/PD-L1 inhibitors. The role of PD-L1 expression in tumors with EGFR mutation and its influence on clinical outcomes remain controversial. Methods: Patients with newly diagnosed metastatic NSCLC with sensitizing EGFR muta- tions who received the standard treatment, ie, EGFR-TKIs for mutant adenocarcinoma as the first-line treatment, were enrolled in this retrospective study. EGFR mutations and PD-L1 expression levels were detected by Cobas RT-PCR and Dako 22C3 immunohistochemistry staining, respectively. Results: From January 2011 to February 2019, 114 patients were enrolled. The average age was 62 years (range 34-92), and 45 (39.5%) patients were male. Among these patients, EGFR mutation analysis revealed exon 19 in-frame deletion in 55 (48.2%) patients, exon 21 L858R in 53 (46.5%) patients, and uncommon mutations in 6 (5.3%) patients. Among these patients with EGFR mutations, PD-L1 expression levels by tumor proportion score (TPS) were <1% in 54 (46.9%) patients, 1-49% in 50 (44.2%) patients, and ?50% in 10 (8.8%) patients. All patients received EGFR-TKIs as first-line treatment, and in the Kaplan-Meier analysis, progression-free survival was not significantly different among groups with differ- ent PD-L1 expression status. Conclusion: For patients with metastatic NSCLC and EGFR mutations, PD-L1 expression is not uncommon, but no significant influence on clinical outcomes was observed in patients receiving standard initial treatment. ? 2021 Chang et al.
Subjects
Epidermal growth factor receptor mutation; Epidermal growth factor receptor tyrosine kinase inhibitors; Programmed death-ligand 1
SDGs

[SDGs]SDG3

Other Subjects
afatinib; bevacizumab; epidermal growth factor receptor; erlotinib; gefitinib; programmed death 1 ligand 1; ramucirumab; adult; aged; Article; clinical outcome; EGFR gene; exon; female; gene deletion; gene mutation; human; major clinical study; male; metastasis; non small cell lung cancer; overall survival; progression free survival; protein expression; retrospective study; very elderly
Publisher
Dove Medical Press Ltd
Type
journal article

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