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A Case Report of EGFR-TKIs Resistant Secondary MET Gene Amplified Lung Squamous Cell Carcinoma and Literature Review

Authors :
Yalan LIU
Peng CHEN
Xinfu LIU
Source :
Chinese Journal of Lung Cancer, Vol 27, Iss 11, Pp 878-884 (2024)
Publication Year :
2024
Publisher :
Chinese Anti-Cancer Association; Chinese Antituberculosis Association, 2024.

Abstract

With the rapid development of epidermal growth factor receptor (EGFR) gene testing of lung adenocarcinoma patients has been routinely carried out, EGFR mutations are also possible for some small samples of non-smoking female lung squamous cell carcinoma patients. This increases the opportunity for targeted therapy for this group of patients. However, drug resistance in patients with lung squamous cell carcinoma during targeted therapy is an important factor affecting subsequent treatment. There are multiple mechanisms of acquired drug resistance in targeted therapy, and the alteration of mesenchymal-epithelial transition factor (MET) signaling pathway is one of the common mechanisms of drug resistance. At present, some selective tyrosine kinase inhibitors (TKIs) of MET has been approved for non-small cell lung cancer with MET gene 14 exon skipping mutation, such as Glumetinib, Savolitinib, Tepotinib, Capmatinib, etc. Drugs that target secondary MET amplification are still in clinical trials. This paper retrospectively analyzed the clinical data of a female patient with EGFR-TKIs resistant secondary MET amplified squamous cell lung cancer, and reviewed relevant literature to explore how to optimize the treatment of lung squamous cell carcinoma patients with EGFR mutation, so as to provide clinical reference for the diagnosis and treatment of such patients.

Details

Language :
Chinese
ISSN :
10093419 and 19996187
Volume :
27
Issue :
11
Database :
Directory of Open Access Journals
Journal :
Chinese Journal of Lung Cancer
Publication Type :
Academic Journal
Accession number :
edsdoj.0e00f692dc84a4cb19246a56908698e
Document Type :
article
Full Text :
https://doi.org/10.3779/j.issn.1009-3419.2024.106.32