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MET alterations in NSCLC-Current Perspectives and Future Challenges.
Remon, Jordi; Hendriks, Lizza E L; Mountzios, Giannis; García-Campelo, Rosario; Saw, Stephanie P L; Uprety, Dipesh; Recondo, Gonzalo; Villacampa, Guillermo; Reck, Martin.
Affiliation
  • Remon J; Department of Cancer Medicine, Gustave Roussy, Villejuif, France. Electronic address: JORDI.REMON-MASIP@gustaveroussy.fr.
  • Hendriks LEL; Department of Respiratory Medicine, Maastricht University Medical Centre, GROW School for Oncology and Reproduction, Maastricht, the Netherlands.
  • Mountzios G; Fourth Department of Medical Oncology and Clinical Trials Unit, Henry Dunant Hospital Center, Athens, Greece.
  • García-Campelo R; Department of Medical Oncology, Hospital Universitario A Coruña, A Coruña, Spain.
  • Saw SPL; Department of Medical Oncology, National Cancer Centre Singapore, Duke- National University of Singapore (NUS) Oncology Academic Clinical Programme, Singapore.
  • Uprety D; Department of Medical Oncology, Karmanos Cancer Institute, Detroit, Michigan.
  • Recondo G; Thoracic Oncology Unit, Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno", Buenos Aires, Argentina.
  • Villacampa G; Oncology Data Science, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain; The Institute of Cancer Research, London, United Kingdom.
  • Reck M; Department of Thoracic Oncology, Airway Research Center North, German Center of Lung Research, Lung Clinic, Grosshansdorf, Germany.
J Thorac Oncol ; 18(4): 419-435, 2023 04.
Article in En | MEDLINE | ID: mdl-36441095
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / Lung Neoplasms Limits: Humans Language: En Journal: J Thorac Oncol Year: 2023 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / Lung Neoplasms Limits: Humans Language: En Journal: J Thorac Oncol Year: 2023 Document type: Article Country of publication: United States