ALK-tyrosine kinase inhibitor intrinsic resistance due to

ALK-rearranged non-small cell lung cancer (ALK-rearranged NSCLC) De novo MET-amplification case report intrinsic ALK-tyrosine kinase inhibitor resistance (intrinsic ALK-TKI resistance) tyrosine kinase inhibitor combination (TKI combination)

Journal

Translational lung cancer research
ISSN: 2218-6751
Titre abrégé: Transl Lung Cancer Res
Pays: China
ID NLM: 101646875

Informations de publication

Date de publication:
30 Sep 2024
Historique:
received: 20 05 2024
accepted: 26 07 2024
medline: 21 10 2024
pubmed: 21 10 2024
entrez: 21 10 2024
Statut: ppublish

Résumé

Most patients with advanced anaplastic lymphoma kinase ( A 43-year-old, female diagnosed with T4N3M1c NSCLC harboring the echinoderm microtubule-associated protein-like 4 ( The combination of alectinib and crizotinib may be a feasible and effective treatment for

Sections du résumé

Background UNASSIGNED
Most patients with advanced anaplastic lymphoma kinase (
Case Description UNASSIGNED
A 43-year-old, female diagnosed with T4N3M1c NSCLC harboring the echinoderm microtubule-associated protein-like 4 (
Conclusions UNASSIGNED
The combination of alectinib and crizotinib may be a feasible and effective treatment for

Identifiants

pubmed: 39430327
doi: 10.21037/tlcr-24-439
pii: tlcr-13-09-2453
pmc: PMC11484720
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Pagination

2453-2462

Informations de copyright

2024 AME Publishing Company. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://tlcr.amegroups.com/article/view/10.21037/tlcr-24-439/coif). E.M.U. reports research grants from AstraZeneca and Merck; speaker fees from Amgen, AstraZeneca, Janssen and Novartis; travel support related to participation in international scientific meeting from AstraZeneca and Roche; payment for participation in Advisory Board from AstraZeneca, Pfizer, Roche and Takeda. M.G. reports speaker fees from Amgen, AstraZeneca, Boehringer Ingelheim and ThermoFisher Scientific, and received research grants from Merck and Roche. J.B.S. received consulting fees from AstraZeneca, Bristol-Myers Squibb, Merck, Janssen, Roche; received honoraria for lectures from Bristol-Myers Squibb, Janssen; received support for attending meetings and/or travel from AstraZeneca, Janssen, Merck; and received payment for participation in Advisory Board from AstraZeneca, Bristol-Myers Squibb, Genmab, Janssen, Merck, Roche. E.S.R. received research grants from Sanofi and Takeda; reports honoraria for lectures from Amgen, AstraZeneca, Bayer, Bristol-Myers Squibb, Roche, Takeda; and received payment for participation in Advisory Board from Roche and Takeda. The other authors have no conflicts of interest to declare.

Auteurs

Edyta M Urbanska (EM)

Department of Oncology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Morten Grauslund (M)

Department of Pathology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Siv M S Berger (SMS)

Department of Radiology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Junia C Costa (JC)

Department of Radiology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Peter R Koffeldt (PR)

Department of Pathology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Jens B Sørensen (JB)

Department of Oncology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Eric Santoni-Rugiu (E)

Department of Pathology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Classifications MeSH