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Targeted Therapies for Melanoma Brain Metastases
Brain metastases are a major clinical challenge occurring in up to 60% of patients suffering from metastatic melanoma. They cause significant clinical symptoms and impair the overall survival prognosis. The introduction of targeted therapies including BRAF and MEK inhibitors as well as CTLA-4 and PD...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378732/ https://www.ncbi.nlm.nih.gov/pubmed/28374234 http://dx.doi.org/10.1007/s11940-017-0449-2 |
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author | Berghoff, Anna S. Preusser, Matthias |
author_facet | Berghoff, Anna S. Preusser, Matthias |
author_sort | Berghoff, Anna S. |
collection | PubMed |
description | Brain metastases are a major clinical challenge occurring in up to 60% of patients suffering from metastatic melanoma. They cause significant clinical symptoms and impair the overall survival prognosis. The introduction of targeted therapies including BRAF and MEK inhibitors as well as CTLA-4 and PD-1 axis targeting immune checkpoint inhibitors have dramatically improved the treatment and prognosis of patients with extracranial metastatic melanoma. Although, similar response rates for extra- and intracranial metastases have been reported, only few data from brain metastasis specific trails are available so far. The following review will provide an overview on the currently available data on targeted therapies, remaining questions and the most important side effects in the special clinical situation of melanoma brain metastases. |
format | Online Article Text |
id | pubmed-5378732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-53787322017-04-25 Targeted Therapies for Melanoma Brain Metastases Berghoff, Anna S. Preusser, Matthias Curr Treat Options Neurol Neuro-oncology (R Soffietti, Section Editor) Brain metastases are a major clinical challenge occurring in up to 60% of patients suffering from metastatic melanoma. They cause significant clinical symptoms and impair the overall survival prognosis. The introduction of targeted therapies including BRAF and MEK inhibitors as well as CTLA-4 and PD-1 axis targeting immune checkpoint inhibitors have dramatically improved the treatment and prognosis of patients with extracranial metastatic melanoma. Although, similar response rates for extra- and intracranial metastases have been reported, only few data from brain metastasis specific trails are available so far. The following review will provide an overview on the currently available data on targeted therapies, remaining questions and the most important side effects in the special clinical situation of melanoma brain metastases. Springer US 2017-04-03 2017 /pmc/articles/PMC5378732/ /pubmed/28374234 http://dx.doi.org/10.1007/s11940-017-0449-2 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Neuro-oncology (R Soffietti, Section Editor) Berghoff, Anna S. Preusser, Matthias Targeted Therapies for Melanoma Brain Metastases |
title | Targeted Therapies for Melanoma Brain Metastases |
title_full | Targeted Therapies for Melanoma Brain Metastases |
title_fullStr | Targeted Therapies for Melanoma Brain Metastases |
title_full_unstemmed | Targeted Therapies for Melanoma Brain Metastases |
title_short | Targeted Therapies for Melanoma Brain Metastases |
title_sort | targeted therapies for melanoma brain metastases |
topic | Neuro-oncology (R Soffietti, Section Editor) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378732/ https://www.ncbi.nlm.nih.gov/pubmed/28374234 http://dx.doi.org/10.1007/s11940-017-0449-2 |
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