| Literature DB >> 26047622 |
Umberto Malapelle1, Simona Vatrano2, Stefania Russo1, Claudio Bellevicine1, Caterina de Luca1, Roberta Sgariglia1, Danilo Rocco3, Livia de Pietro3, Fernando Riccardi4, Elisa Gobbini2, Luisella Righi2, Giancarlo Troncone1.
Abstract
In non-small cell lung cancer (NSCLC), the epidermal growth factor receptor (EGFR) gene may undergo both mutations and copy number gains. EGFR mutant allele-specific imbalance (MASI) occurs when the ratio of mutant-to-wild-type alleles increases significantly. In this study, by using a previously validated microfluidic-chip-based technology, EGFR-MASI occurred in 25/67 mutant cases (37%), being more frequently associated with EGFR exon 19 deletions (p=0.033). In a subset of 49 treated patients, we assessed whether MASI is a modifier of anti-EGFR treatment benefit. The difference in progression-free survival and overall survival between EGFR-MASI-positive and EGFR-MASI-negative groups of patients did not show a statistical significance. In conclusion, EGFR-MASI is a significant event in NSCLC, specifically associated with EGFR exon 19 deletions. However, EGFR-MASI does not seem to play a role in predicting the response to first-generation EGFR small molecules inhibitors. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.Entities:
Keywords: EGFR; MOLECULAR PATHOLOGY; TUMOUR MARKERS
Mesh:
Year: 2015 PMID: 26047622 DOI: 10.1136/jclinpath-2015-203101
Source DB: PubMed Journal: J Clin Pathol ISSN: 0021-9746 Impact factor: 3.411