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Response to Capmatinib in a MET Fusion-positive Cholangiocarcinoma

Cholangiocarcinoma is the second most common liver cancer after hepatocellular carcinoma. In case of metastatic or unresectable disease, the recommended first-line treatment is gemcitabine-based doublet, most commonly gemcitabine and cisplatin. There is no standard treatment for further lines. MET f...

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Autores principales: Turpin, Anthony, Descarpentries, Clotilde, Grégoire, Valérie, Farchi, Olivier, Cortot, Alexis B, Jamme, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847551/
https://www.ncbi.nlm.nih.gov/pubmed/36434677
http://dx.doi.org/10.1093/oncolo/oyac194
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author Turpin, Anthony
Descarpentries, Clotilde
Grégoire, Valérie
Farchi, Olivier
Cortot, Alexis B
Jamme, Philippe
author_facet Turpin, Anthony
Descarpentries, Clotilde
Grégoire, Valérie
Farchi, Olivier
Cortot, Alexis B
Jamme, Philippe
author_sort Turpin, Anthony
collection PubMed
description Cholangiocarcinoma is the second most common liver cancer after hepatocellular carcinoma. In case of metastatic or unresectable disease, the recommended first-line treatment is gemcitabine-based doublet, most commonly gemcitabine and cisplatin. There is no standard treatment for further lines. MET fusions are rare alterations described in many cancers. The efficacy of specific MET inhibitors is poorly studied. We present the case of a patient with chemotherapy-refractory metastatic cholangiocarcinoma harboring a CAPZA-2-MET fusion along with MET amplification who dramatically responded to capmatinib, a specific MET tyrosine kinase inhibitor.
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spelling pubmed-98475512023-01-20 Response to Capmatinib in a MET Fusion-positive Cholangiocarcinoma Turpin, Anthony Descarpentries, Clotilde Grégoire, Valérie Farchi, Olivier Cortot, Alexis B Jamme, Philippe Oncologist Precision Medicine Clinic: Molecular Tumor Board Cholangiocarcinoma is the second most common liver cancer after hepatocellular carcinoma. In case of metastatic or unresectable disease, the recommended first-line treatment is gemcitabine-based doublet, most commonly gemcitabine and cisplatin. There is no standard treatment for further lines. MET fusions are rare alterations described in many cancers. The efficacy of specific MET inhibitors is poorly studied. We present the case of a patient with chemotherapy-refractory metastatic cholangiocarcinoma harboring a CAPZA-2-MET fusion along with MET amplification who dramatically responded to capmatinib, a specific MET tyrosine kinase inhibitor. Oxford University Press 2023-01-18 /pmc/articles/PMC9847551/ /pubmed/36434677 http://dx.doi.org/10.1093/oncolo/oyac194 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Precision Medicine Clinic: Molecular Tumor Board
Turpin, Anthony
Descarpentries, Clotilde
Grégoire, Valérie
Farchi, Olivier
Cortot, Alexis B
Jamme, Philippe
Response to Capmatinib in a MET Fusion-positive Cholangiocarcinoma
title Response to Capmatinib in a MET Fusion-positive Cholangiocarcinoma
title_full Response to Capmatinib in a MET Fusion-positive Cholangiocarcinoma
title_fullStr Response to Capmatinib in a MET Fusion-positive Cholangiocarcinoma
title_full_unstemmed Response to Capmatinib in a MET Fusion-positive Cholangiocarcinoma
title_short Response to Capmatinib in a MET Fusion-positive Cholangiocarcinoma
title_sort response to capmatinib in a met fusion-positive cholangiocarcinoma
topic Precision Medicine Clinic: Molecular Tumor Board
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847551/
https://www.ncbi.nlm.nih.gov/pubmed/36434677
http://dx.doi.org/10.1093/oncolo/oyac194
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