Ontology highlight
ABSTRACT: Background
Mesenchymal-to-epithelial transition (MET) exon 14 skipping mutations and MET gene amplification occur in 3-5% of non-small cell lung cancer (NSCLC) patients. Tyrosine kinase inhibitors (TKIs) targeting MET alterations have shown promising results in these patients.Objective
The aim of this study was to describe the genomic profile, PD-L1 expression and clinicopathological features of MET dysregulated NSCLC.Patients and methods
We identified 188 patients with advanced-stage NSCLC with data on MET expression by immunohistochemistry (IHC). IHC for PD-L1 expression was performed in 131 patient samples, and next-generation sequencing (NGS) analysis was performed in 109 patient samples.Results
MET exon 14 skipping alterations were identified in 16 (14.
SUBMITTER: Fischer A
PROVIDER: S-EPMC9684265 | biostudies-literature | 2022 Nov
REPOSITORIES: biostudies-literature