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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Future Science Ltd
2015
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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. |
format | Online Article Text |
id | pubmed-5137998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Future Science Ltd |
record_format | MEDLINE/PubMed |
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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