TY - JOUR
T1 - MET alterations in NSCLC—Current Perspectives and Future Challenges
AU - Remon, Jordi
AU - Hendriks, Lizza E.L.
AU - Mountzios, Giannis
AU - García-Campelo, Rosario
AU - Saw, Stephanie P.L.
AU - Uprety, Dipesh
AU - Recondo, Gonzalo
AU - Villacampa, Guillermo
AU - Reck, Martin
N1 - Publisher Copyright:
© 2022 International Association for the Study of Lung Cancer
PY - 2023/4/1
Y1 - 2023/4/1
N2 - Targeted therapies have revolutionized the treatment and improved the outcome for oncogene-driven NSCLC and an increasing number of oncogenic driver therapies have become available. For MET-dysregulated NSCLC (especially MET exon 14 skipping mutations and MET-amplifications, which is one of the most common bypass mechanisms of resistance in oncogene-addicted NSCLC), several anti–MET-targeted therapies have been approved recently (MET exon 14 skipping mutation) and multiple others are in development. In this narrative review, we summarize the role of MET as an oncogenic driver in NSCLC, discuss the different testing methods for exon 14 skipping mutations, gene amplification, and protein overexpression, and review the existing data and ongoing clinical trials regarding targeted therapies in MET-altered NSCLC. As immunotherapy with or without chemotherapy has become the standard of care for advanced NSCLC, immunotherapy data for MET-dysregulated NSCLC are put into perspective. Finally, we discuss future challenges in this rapidly evolving landscape.
AB - Targeted therapies have revolutionized the treatment and improved the outcome for oncogene-driven NSCLC and an increasing number of oncogenic driver therapies have become available. For MET-dysregulated NSCLC (especially MET exon 14 skipping mutations and MET-amplifications, which is one of the most common bypass mechanisms of resistance in oncogene-addicted NSCLC), several anti–MET-targeted therapies have been approved recently (MET exon 14 skipping mutation) and multiple others are in development. In this narrative review, we summarize the role of MET as an oncogenic driver in NSCLC, discuss the different testing methods for exon 14 skipping mutations, gene amplification, and protein overexpression, and review the existing data and ongoing clinical trials regarding targeted therapies in MET-altered NSCLC. As immunotherapy with or without chemotherapy has become the standard of care for advanced NSCLC, immunotherapy data for MET-dysregulated NSCLC are put into perspective. Finally, we discuss future challenges in this rapidly evolving landscape.
KW - Amivantamab
KW - Capmatinib
KW - MET amplified
KW - MET exon 14
KW - Non–small cell lung cancer
KW - Tepotinib
UR - http://www.scopus.com/inward/record.url?scp=85142761559&partnerID=8YFLogxK
U2 - 10.1016/j.jtho.2022.10.015
DO - 10.1016/j.jtho.2022.10.015
M3 - Review article
C2 - 36441095
AN - SCOPUS:85142761559
SN - 1556-0864
VL - 18
SP - 419
EP - 435
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 4
ER -