Programmed Death-Ligand 1 Expression Predicts Tyrosine Kinase Inhibitor Response and Better Prognosis in a Cohort of Patients With Epidermal Growth Factor Receptor Mutation-Positive Lung Adenocarcinoma
Micro-Abstract The oncogenic driver epidermal growth factor receptor (EGFR) mutations upregulate immune checkpoint proteins programmed death-1 (PD-1)/programmed death-ligand 1 (PD-L1) in in vitro and in vivo models of non–small-cell lung cancer (NSCLC). Immunohistochemistry revealed that PD-L1 and P...
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Veröffentlicht in: | Clinical lung cancer 2015-09, Vol.16 (5), p.e25-e35 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Micro-Abstract The oncogenic driver epidermal growth factor receptor (EGFR) mutations upregulate immune checkpoint proteins programmed death-1 (PD-1)/programmed death-ligand 1 (PD-L1) in in vitro and in vivo models of non–small-cell lung cancer (NSCLC). Immunohistochemistry revealed that PD-L1 and PD-1 were positive in 53.6% and 32.1% of tumor specimens in a cohort of 56 patients with NSCLC carrying EGFR mutations, respectively. PD-L1 expression correlated with a better response to EGFR tyrosine kinase inhibitors and longer survival. |
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ISSN: | 1525-7304 1938-0690 |
DOI: | 10.1016/j.cllc.2015.02.002 |