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Vemurafenib: a new treatment for BRAF-V600 mutated advanced melanoma
The BRAF inhibitor, vemurafenib, has demonstrated improved progression-free and overall survival compared with chemotherapy in a randomized trial, and represents a new standard of care in patients with advanced melanoma harboring a BRAF-V600 mutation. A BRAF-V600 mutation is identified in approximat...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3421463/ https://www.ncbi.nlm.nih.gov/pubmed/22904646 http://dx.doi.org/10.2147/CMAR.S25284 |
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author | Fisher, Rosalie Larkin, James |
author_facet | Fisher, Rosalie Larkin, James |
author_sort | Fisher, Rosalie |
collection | PubMed |
description | The BRAF inhibitor, vemurafenib, has demonstrated improved progression-free and overall survival compared with chemotherapy in a randomized trial, and represents a new standard of care in patients with advanced melanoma harboring a BRAF-V600 mutation. A BRAF-V600 mutation is identified in approximately half of patients with cutaneous melanoma, and is unequivocally a biomarker predictive of profound clinical benefit for these patients. However, acquired vemurafenib resistance is a major clinical challenge and therapy is not yet curative. A substantial body of translational research has been performed alongside clinical trials of vemurafenib, providing key insights into the molecular basis of response and resistance. This review summarizes the development of vemurafenib for the treatment of BRAF-V600 mutant melanoma and discusses how knowledge of critical signaling pathways will be applied for its optimal clinical use in future. |
format | Online Article Text |
id | pubmed-3421463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34214632012-08-19 Vemurafenib: a new treatment for BRAF-V600 mutated advanced melanoma Fisher, Rosalie Larkin, James Cancer Manag Res Review The BRAF inhibitor, vemurafenib, has demonstrated improved progression-free and overall survival compared with chemotherapy in a randomized trial, and represents a new standard of care in patients with advanced melanoma harboring a BRAF-V600 mutation. A BRAF-V600 mutation is identified in approximately half of patients with cutaneous melanoma, and is unequivocally a biomarker predictive of profound clinical benefit for these patients. However, acquired vemurafenib resistance is a major clinical challenge and therapy is not yet curative. A substantial body of translational research has been performed alongside clinical trials of vemurafenib, providing key insights into the molecular basis of response and resistance. This review summarizes the development of vemurafenib for the treatment of BRAF-V600 mutant melanoma and discusses how knowledge of critical signaling pathways will be applied for its optimal clinical use in future. Dove Medical Press 2012-08-08 /pmc/articles/PMC3421463/ /pubmed/22904646 http://dx.doi.org/10.2147/CMAR.S25284 Text en © 2012 Fisher and Larkin, 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 Fisher, Rosalie Larkin, James Vemurafenib: a new treatment for BRAF-V600 mutated advanced melanoma |
title | Vemurafenib: a new treatment for BRAF-V600 mutated advanced melanoma |
title_full | Vemurafenib: a new treatment for BRAF-V600 mutated advanced melanoma |
title_fullStr | Vemurafenib: a new treatment for BRAF-V600 mutated advanced melanoma |
title_full_unstemmed | Vemurafenib: a new treatment for BRAF-V600 mutated advanced melanoma |
title_short | Vemurafenib: a new treatment for BRAF-V600 mutated advanced melanoma |
title_sort | vemurafenib: a new treatment for braf-v600 mutated advanced melanoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3421463/ https://www.ncbi.nlm.nih.gov/pubmed/22904646 http://dx.doi.org/10.2147/CMAR.S25284 |
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