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Clinical activity of regorafenib in PDGFRA-mutated gastrointestinal stromal tumor

Gastrointestinal stromal tumor (GIST) is the most frequent mesenchymal tumor of the gastrointestinal tract and one of the most frequent sarcoma. Mutually exclusive KIT and PDGFRA mutations are central events in GIST pathogenesis, and their understanding is crucial because specific treatment targetin...

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Autores principales: Grellety, Thomas, Kind, Michèle, Coindre, Jean-Michel, Italiano, Antoine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137998/
https://www.ncbi.nlm.nih.gov/pubmed/28031906
http://dx.doi.org/10.4155/fso.15.33
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author Grellety, Thomas
Kind, Michèle
Coindre, Jean-Michel
Italiano, Antoine
author_facet Grellety, Thomas
Kind, Michèle
Coindre, Jean-Michel
Italiano, Antoine
author_sort Grellety, Thomas
collection PubMed
description Gastrointestinal stromal tumor (GIST) is the most frequent mesenchymal tumor of the gastrointestinal tract and one of the most frequent sarcoma. Mutually exclusive KIT and PDGFRA mutations are central events in GIST pathogenesis, and their understanding is crucial because specific treatment targeting oncogenic KIT and PDGFRA activation (especially imatinib) has become available. The most frequent PDGFRA mutation (D842V) is associated with primary resistance to imatinib. Data related to regorafenib efficacy in PDGFRA-mutated GIST are lacking. We report here a case report of a prolonged response with regorafenib in a patient with a PDGFRA-mutated GIST.
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spelling pubmed-51379982016-12-28 Clinical activity of regorafenib in PDGFRA-mutated gastrointestinal stromal tumor Grellety, Thomas Kind, Michèle Coindre, Jean-Michel Italiano, Antoine Future Sci OA Case Report Gastrointestinal stromal tumor (GIST) is the most frequent mesenchymal tumor of the gastrointestinal tract and one of the most frequent sarcoma. Mutually exclusive KIT and PDGFRA mutations are central events in GIST pathogenesis, and their understanding is crucial because specific treatment targeting oncogenic KIT and PDGFRA activation (especially imatinib) has become available. The most frequent PDGFRA mutation (D842V) is associated with primary resistance to imatinib. Data related to regorafenib efficacy in PDGFRA-mutated GIST are lacking. We report here a case report of a prolonged response with regorafenib in a patient with a PDGFRA-mutated GIST. Future Science Ltd 2015-11-01 /pmc/articles/PMC5137998/ /pubmed/28031906 http://dx.doi.org/10.4155/fso.15.33 Text en © Antoine Italiano This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Case Report
Grellety, Thomas
Kind, Michèle
Coindre, Jean-Michel
Italiano, Antoine
Clinical activity of regorafenib in PDGFRA-mutated gastrointestinal stromal tumor
title Clinical activity of regorafenib in PDGFRA-mutated gastrointestinal stromal tumor
title_full Clinical activity of regorafenib in PDGFRA-mutated gastrointestinal stromal tumor
title_fullStr Clinical activity of regorafenib in PDGFRA-mutated gastrointestinal stromal tumor
title_full_unstemmed Clinical activity of regorafenib in PDGFRA-mutated gastrointestinal stromal tumor
title_short Clinical activity of regorafenib in PDGFRA-mutated gastrointestinal stromal tumor
title_sort clinical activity of regorafenib in pdgfra-mutated gastrointestinal stromal tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137998/
https://www.ncbi.nlm.nih.gov/pubmed/28031906
http://dx.doi.org/10.4155/fso.15.33
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