Safety of MET Tyrosine Kinase Inhibitors in Patients With MET Exon 14 Skipping Non-small Cell Lung Cancer: A Clinical Review.


Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
05 2022
Historique:
received: 19 11 2021
revised: 20 01 2022
accepted: 20 01 2022
pubmed: 12 3 2022
medline: 18 5 2022
entrez: 11 3 2022
Statut: ppublish

Résumé

MET exon 14 (METex14) skipping mutations occur in 3% to 4% of non-small cell lung cancer (NSCLC) cases. Currently, four oral MET tyrosine kinase inhibitors (TKIs) are in use for the treatment of patients with METex14 skipping NSCLC (tepotinib, capmatinib, savolitinib, and crizotinib). To support optimal management of METex14 skipping NSCLC in this typically older patient population, the safety profiles of these treatment options are reviewed here. Published safety data from prospective clinical trials with MET TKIs in patients with METex14 skipping NSCLC were reviewed. Treatment-related adverse events (TRAEs) occurring in ≥ 10% of patients were reported where feasible. Guidance on clinical monitoring and management of key MET TKI TRAEs and drug-drug interactions is provided. Across the clinical trials, safety data for MET TKIs were reported for 442 patients with METex14 skipping. Peripheral edema was the most reported TRAE (50%-63% of patients; grade ≥ 3: 1%-11%), followed by nausea (26%-46% of patients; grade ≥ 3: 0%-1%). TRAEs led to dose reductions in 33% to 38% of patients and to discontinuation in 7% to 14% of patients, across the MET TKIs. Considerations on interpreting available safety data are provided, along with insights into monitoring and managing specific MET TKI TRAEs of interest and drug-drug interactions. Overall, MET TKIs are tolerable treatment options for patients with METex14 skipping NSCLC, an older population for whom chemo- or immuno-therapy may not be an effective nor tolerable option. More data regarding the effectiveness of safety interventions and management strategies are needed.

Identifiants

pubmed: 35272955
pii: S1525-7304(22)00013-4
doi: 10.1016/j.cllc.2022.01.003
pii:
doi:

Substances chimiques

Protein Kinase Inhibitors 0
Proto-Oncogene Proteins c-met EC 2.7.10.1

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

195-207

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Alexis Cortot (A)

Université de Lille, CHU Lille, Thoracic Oncology Department, Centre National de la Recherche Scientifique, INSERM, Institut Pasteur de Lille, UMR9020-UMR-S 1277-Canther, Lille, France. Electronic address: alexis.cortot@chru-lille.fr.

Xiuning Le (X)

M.D. Anderson Cancer Center, University of Texas, Houston, TX.

Egbert Smit (E)

Department of Thoracic Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Santiago Viteri (S)

Instituto Oncológico Dr. Rosell. Hospital Universitari Dexeus, Grupo QuironSalud, Barcelona, Spain.

Terufumi Kato (T)

Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan.

Hiroshi Sakai (H)

Department of Thoracic Oncology, Ageo Central General Hospital, Ageo, Japan.

Keunchil Park (K)

Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

D Ross Camidge (DR)

University of Colorado, Aurora, CO.

Karin Berghoff (K)

The healthcare business of Merck KGaA, Darmstadt, Germany.

Soetkin Vlassak (S)

The healthcare business of Merck KGaA, Darmstadt, Germany.

Paul K Paik (PK)

Weill Cornell Medical College, New York, NY; Memorial Sloan Kettering Cancer Center, New York, NY.

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Classifications MeSH