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Case report: BRAF A598-T599insV mutation as a potential resistance mechanism to alectinib in ALK-rearranged lung adenocarcinoma.

Authors :
UCL - SSS/IREC/MONT - Pôle Mont Godinne
UCL - (MGD) Service de pneumologie
UCL - (MGD) Service d'anatomie pathologique
UCL - (MGD) Service de médecine nucléaire
UCL - (MGD) Service de chirurgie cardio-vasculaire et thoracique
UCL - (MGD) Service de radiologie - résonance magnétique
UCL - SSS/IREC/PNEU - Pôle de Pneumologie, ORL et Dermatologie
Pasau, Thomas
Wauters, Els
Wauters, Isabelle
Duplaquet, Fabrice
Pirard, Lionel
STANCIU POP, Claudia Maria
D'Haene, Nicky
Dupont, Michaël
Vander Borght, Thierry
Rondelet, Benoît
Ocak, Sebahat
UCL - SSS/IREC/MONT - Pôle Mont Godinne
UCL - (MGD) Service de pneumologie
UCL - (MGD) Service d'anatomie pathologique
UCL - (MGD) Service de médecine nucléaire
UCL - (MGD) Service de chirurgie cardio-vasculaire et thoracique
UCL - (MGD) Service de radiologie - résonance magnétique
UCL - SSS/IREC/PNEU - Pôle de Pneumologie, ORL et Dermatologie
Pasau, Thomas
Wauters, Els
Wauters, Isabelle
Duplaquet, Fabrice
Pirard, Lionel
STANCIU POP, Claudia Maria
D'Haene, Nicky
Dupont, Michaël
Vander Borght, Thierry
Rondelet, Benoît
Ocak, Sebahat
Source :
Frontiers in oncology, Vol. 12, p. 985446 (2022)
Publication Year :
2022

Abstract

Anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitors (TKIs) have improved the prognosis of advanced-stage non-small cell lung cancer (NSCLC) with ALK rearrangement, but resistance mechanisms limit their efficacy. We describe the case of a 63-year-old man with a stage cIVA -rearranged lung adenocarcinoma who developed a A598-T599insV mutation as a potential resistance mechanism to alectinib, a second-generation ALK TKI. He was treated with an association of BRAF and MEK inhibitors but death occurred two months after treatment initiation in a context of tumor progression and toxicity. Based on this first report of A598-T599insV mutation occurring in lung cancer, we discuss resistance mechanisms to ALK TKIs, implications of mutation in NSCLC, and A598-T599insV mutation in other cancers.

Details

Database :
OAIster
Journal :
Frontiers in oncology, Vol. 12, p. 985446 (2022)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1372936747
Document Type :
Electronic Resource