Response to MET Inhibitors in Patients with Stage IV Lung Adenocarcinomas Harboring MET Mutations Causing Exon 14 Skipping
Memorial Sloan Kettering Cancer Center · Cornell University
Abstract
UNLABELLED: Mutations in the MET exon 14 RNA splice acceptor and donor sites, which lead to exon skipping, deletion of the juxtamembrane domain containing the CBL E3-ubiquitin ligase-binding site, and decreased turnover of the resultant aberrant MET protein, were previously reported to be oncogenic in preclinical models. We now report responses to the MET inhibitors crizotinib and cabozantinib in four patients with stage IV lung adenocarcinomas harboring mutations leading to MET exon 14 skipping, highlighting a new therapeutic strategy for the 4% of lung adenocarcinoma patients whose tumors harbor this previously underappreciated genetic alteration. SIGNIFICANCE: Oncogenic mutations in the MET exon 14 splice…
Citation impact
- FWCI
- 58.70
- Percentile
- 100%
- References
- 26
Authors
11- PKPaul K. PaikCorresponding
Memorial Sloan Kettering Cancer Center, Cornell University
- ADAlexander Drilon
Memorial Sloan Kettering Cancer Center, Cornell University
- PFPang‐Dian Fan
Memorial Sloan Kettering Cancer Center
- HAHelena A. Yu
Memorial Sloan Kettering Cancer Center, Cornell University
- NRNatasha Rekhtman
Memorial Sloan Kettering Cancer Center
Topics & keywords
- Exon
- Crizotinib
- Exon skipping
- Cabozantinib
- Cancer research
- Adenocarcinoma
- Biology
- Lung cancer
- Good health and well-being