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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Clinical lung cancer 2015-09, Vol.16 (5), p.e25-e35
Hauptverfasser: Lin, Cheng, Chen, Xiong, Li, Meifang, Liu, Jingnan, Qi, Xingfeng, Yang, Wenting, Zhang, Hairong, Cai, Zhongfu, Dai, Yun, Ouyang, Xuenong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
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.
ISSN:1525-7304
1938-0690
DOI:10.1016/j.cllc.2015.02.002