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Metastatic melanoma and vemurafenib: novel approaches
Metastatic melanoma (MM) presents a treatment challenge to oncologists worldwide. Dacarbazine is the first line chemotherapy treatment for MM, though the overall response rates are very poor. Recently, the v-raf murine sarcoma viral oncogene homolog B1 (BRAF) V600 mutation was found to play a main r...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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PAGEPress Publications
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401159/ https://www.ncbi.nlm.nih.gov/pubmed/22826788 http://dx.doi.org/10.4081/rt.2012.e31 |
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author | De Mello, Ramon Andrade |
author_facet | De Mello, Ramon Andrade |
author_sort | De Mello, Ramon Andrade |
collection | PubMed |
description | Metastatic melanoma (MM) presents a treatment challenge to oncologists worldwide. Dacarbazine is the first line chemotherapy treatment for MM, though the overall response rates are very poor. Recently, the v-raf murine sarcoma viral oncogene homolog B1 (BRAF) V600 mutation was found to play a main role in MM. This mutation is present in 40–60% of melanoma patients. Vemurafenib is a BRAF kinase inhibitor that showed impressive results in phase I-III trials and was thus recently approved for the treatment of MM. This paper will briefly focus on vemurafenib in the treatment of MM and highlight concerns |
format | Online Article Text |
id | pubmed-3401159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | PAGEPress Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-34011592012-07-23 Metastatic melanoma and vemurafenib: novel approaches De Mello, Ramon Andrade Rare Tumors Editorial Metastatic melanoma (MM) presents a treatment challenge to oncologists worldwide. Dacarbazine is the first line chemotherapy treatment for MM, though the overall response rates are very poor. Recently, the v-raf murine sarcoma viral oncogene homolog B1 (BRAF) V600 mutation was found to play a main role in MM. This mutation is present in 40–60% of melanoma patients. Vemurafenib is a BRAF kinase inhibitor that showed impressive results in phase I-III trials and was thus recently approved for the treatment of MM. This paper will briefly focus on vemurafenib in the treatment of MM and highlight concerns PAGEPress Publications 2012-05-17 /pmc/articles/PMC3401159/ /pubmed/22826788 http://dx.doi.org/10.4081/rt.2012.e31 Text en ©Copyright R.A. De Mello, 2012 This work is licensed under a Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Licensee PAGEPress, Italy |
spellingShingle | Editorial De Mello, Ramon Andrade Metastatic melanoma and vemurafenib: novel approaches |
title | Metastatic melanoma and vemurafenib: novel approaches |
title_full | Metastatic melanoma and vemurafenib: novel approaches |
title_fullStr | Metastatic melanoma and vemurafenib: novel approaches |
title_full_unstemmed | Metastatic melanoma and vemurafenib: novel approaches |
title_short | Metastatic melanoma and vemurafenib: novel approaches |
title_sort | metastatic melanoma and vemurafenib: novel approaches |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401159/ https://www.ncbi.nlm.nih.gov/pubmed/22826788 http://dx.doi.org/10.4081/rt.2012.e31 |
work_keys_str_mv | AT demelloramonandrade metastaticmelanomaandvemurafenibnovelapproaches |