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Agents to treat BRAF-mutant lung cancer

BRAF mutations are seen in up to 3.5–4% of the non-small cell lung cancer (NSCLC) patients. BRAF V600E mutations account for 50% of these cases, and the remaining BRAF mutations are non-V600E. The biologic behavior of BRAF-mutated lung tumors tends to be more aggressive and resistant to chemotherapy...

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Detalles Bibliográficos
Autores principales: Alvarez, Jean G Bustamante, Otterson, Gregory A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioExcel Publishing Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419923/
https://www.ncbi.nlm.nih.gov/pubmed/30899313
http://dx.doi.org/10.7573/dic.212566
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author Alvarez, Jean G Bustamante
Otterson, Gregory A
author_facet Alvarez, Jean G Bustamante
Otterson, Gregory A
author_sort Alvarez, Jean G Bustamante
collection PubMed
description BRAF mutations are seen in up to 3.5–4% of the non-small cell lung cancer (NSCLC) patients. BRAF V600E mutations account for 50% of these cases, and the remaining BRAF mutations are non-V600E. The biologic behavior of BRAF-mutated lung tumors tends to be more aggressive and resistant to chemotherapy, but responses to tyrosine kinase inhibitors such as BRAF inhibitors with or without MEK inhibitors have provided another effective tool to attain better response rates when compared to cytotoxic chemotherapy. New strategies such as immunotherapy are becoming as well another option to treat in the second-line setting patients with BRAF-mutated NSCLC.
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spelling pubmed-64199232019-03-21 Agents to treat BRAF-mutant lung cancer Alvarez, Jean G Bustamante Otterson, Gregory A Drugs Context Review BRAF mutations are seen in up to 3.5–4% of the non-small cell lung cancer (NSCLC) patients. BRAF V600E mutations account for 50% of these cases, and the remaining BRAF mutations are non-V600E. The biologic behavior of BRAF-mutated lung tumors tends to be more aggressive and resistant to chemotherapy, but responses to tyrosine kinase inhibitors such as BRAF inhibitors with or without MEK inhibitors have provided another effective tool to attain better response rates when compared to cytotoxic chemotherapy. New strategies such as immunotherapy are becoming as well another option to treat in the second-line setting patients with BRAF-mutated NSCLC. BioExcel Publishing Ltd 2019-03-13 /pmc/articles/PMC6419923/ /pubmed/30899313 http://dx.doi.org/10.7573/dic.212566 Text en Copyright © 2019 Bustamante Alvarez JG, Otterson GA. Published by Drugs in Context under Creative Commons License Deed CC BY NC ND 4.0 which allows anyone to copy, distribute, and transmit the article provided it is properly attributed in the manner specified below. No commercial use without permission.
spellingShingle Review
Alvarez, Jean G Bustamante
Otterson, Gregory A
Agents to treat BRAF-mutant lung cancer
title Agents to treat BRAF-mutant lung cancer
title_full Agents to treat BRAF-mutant lung cancer
title_fullStr Agents to treat BRAF-mutant lung cancer
title_full_unstemmed Agents to treat BRAF-mutant lung cancer
title_short Agents to treat BRAF-mutant lung cancer
title_sort agents to treat braf-mutant lung cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419923/
https://www.ncbi.nlm.nih.gov/pubmed/30899313
http://dx.doi.org/10.7573/dic.212566
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