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Update on imatinib for gastrointestinal stromal tumors: duration of treatment

Gastrointestinal stromal tumors (GISTs) are the most common sarcoma of the gastrointestinal tract, with transformation typically driven by activating mutations of c-KIT and less commonly platelet-derived growth factor receptor alpha (PDGFRA). Successful targeting of c-KIT and PDGFRA with imatinib, a...

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Detalles Bibliográficos
Autores principales: Linch, Mark, Claus, Jeroen, Benson, Charlotte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735340/
https://www.ncbi.nlm.nih.gov/pubmed/23935374
http://dx.doi.org/10.2147/OTT.S31260
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author Linch, Mark
Claus, Jeroen
Benson, Charlotte
author_facet Linch, Mark
Claus, Jeroen
Benson, Charlotte
author_sort Linch, Mark
collection PubMed
description Gastrointestinal stromal tumors (GISTs) are the most common sarcoma of the gastrointestinal tract, with transformation typically driven by activating mutations of c-KIT and less commonly platelet-derived growth factor receptor alpha (PDGFRA). Successful targeting of c-KIT and PDGFRA with imatinib, a tyrosine kinase inhibitor (TKI), has had a major impact in advanced GIST and as an adjuvant and neoadjuvant treatment. If treatment with imatinib fails, further lines of TKI therapy have a role, but disease response is usually only measured in months, so strategies to maximize the benefit from imatinib are paramount. Here, we provide an overview of the structure and signaling of c-KIT coupled with a review of the clinical trials of imatinib in GIST. In doing so, we make recommendations about the duration of imatinib therapy and suggest how best to utilize imatinib in order to improve patient outcomes in the future.
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spelling pubmed-37353402013-08-09 Update on imatinib for gastrointestinal stromal tumors: duration of treatment Linch, Mark Claus, Jeroen Benson, Charlotte Onco Targets Ther Review Gastrointestinal stromal tumors (GISTs) are the most common sarcoma of the gastrointestinal tract, with transformation typically driven by activating mutations of c-KIT and less commonly platelet-derived growth factor receptor alpha (PDGFRA). Successful targeting of c-KIT and PDGFRA with imatinib, a tyrosine kinase inhibitor (TKI), has had a major impact in advanced GIST and as an adjuvant and neoadjuvant treatment. If treatment with imatinib fails, further lines of TKI therapy have a role, but disease response is usually only measured in months, so strategies to maximize the benefit from imatinib are paramount. Here, we provide an overview of the structure and signaling of c-KIT coupled with a review of the clinical trials of imatinib in GIST. In doing so, we make recommendations about the duration of imatinib therapy and suggest how best to utilize imatinib in order to improve patient outcomes in the future. Dove Medical Press 2013-07-30 /pmc/articles/PMC3735340/ /pubmed/23935374 http://dx.doi.org/10.2147/OTT.S31260 Text en © 2013 Linch et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Linch, Mark
Claus, Jeroen
Benson, Charlotte
Update on imatinib for gastrointestinal stromal tumors: duration of treatment
title Update on imatinib for gastrointestinal stromal tumors: duration of treatment
title_full Update on imatinib for gastrointestinal stromal tumors: duration of treatment
title_fullStr Update on imatinib for gastrointestinal stromal tumors: duration of treatment
title_full_unstemmed Update on imatinib for gastrointestinal stromal tumors: duration of treatment
title_short Update on imatinib for gastrointestinal stromal tumors: duration of treatment
title_sort update on imatinib for gastrointestinal stromal tumors: duration of treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735340/
https://www.ncbi.nlm.nih.gov/pubmed/23935374
http://dx.doi.org/10.2147/OTT.S31260
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