Retrospective Analysis to Optimize the Detection of MET Exon 14 Skipping Mutations in Non-Small Cell Lung Cancer
Author:
Affiliation:
1. Department of Laboratory Medicine, Chang Gung Memorial Hospital, Lin-Kou, 5 Fu-Shing St. Kweishan, Taoyuan 333, Taiwan
2. Department of Medicine, College of Medicine, Chang Gung University, 259 Wen-Hwa 1st Rd. Kweishan, Taoyuan 333, Taiwan
Abstract
Funder
Chang-Gung Memorial Hospital Research Grants
Ministry of Science and Technology, Taiwan
Publisher
MDPI AG
Link
https://www.mdpi.com/2075-4418/14/11/1110/pdf
Reference16 articles.
1. Targeting MET in cancer: Rationale and progress;Gherardi;Nat. Rev. Cancer,2012
2. MET Exon 14 Skipping Mutations in Non-Small-Cell Lung Cancer: An Overview of Biology, Clinical Outcomes, and Testing Considerations;Socinski;JCO Precis. Oncol.,2021
3. MET Amplification and Exon 14 Splice Site Mutation Define Unique Molecular Subgroups of Non-Small Cell Lung Carcinoma with Poor Prognosis;Tong;Clin. Cancer Res.,2016
4. Ding, C., Qiu, Y., Zhang, J., Wei, W., Gao, H., Yuan, Y., and Wang, X. (2023). Clinicopathological characteristics of Non-Small Cell Lung Cancer (NSCLC) patients with c-MET exon 14 skipping mutation, MET overexpression and amplification. BMC Pulm. Med., 23.
5. Nivolumab plus Ipilimumab in Lung Cancer with a High Tumor Mutational Burden;Hellmann;N. Engl. J. Med.,2018
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