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New treatment options for metastatic renal cell carcinoma
During the last decade, the treatment of advanced or metastatic renal cell carcinoma (RCC) was revolutionised with the advent of antiangiogenic drugs and tyrosine-kinase inhibitors. Several agents targeting the vascular endothelial growth factor (VEGF) pathway (sunitinib, bevacizumab, pazopanib, axi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
ESMO Open
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519813/ https://www.ncbi.nlm.nih.gov/pubmed/28761748 http://dx.doi.org/10.1136/esmoopen-2017-000185 |
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author | Rodriguez-Vida, Alejo Hutson, Thomas E Bellmunt, Joaquim Strijbos, Michiel H |
author_facet | Rodriguez-Vida, Alejo Hutson, Thomas E Bellmunt, Joaquim Strijbos, Michiel H |
author_sort | Rodriguez-Vida, Alejo |
collection | PubMed |
description | During the last decade, the treatment of advanced or metastatic renal cell carcinoma (RCC) was revolutionised with the advent of antiangiogenic drugs and tyrosine-kinase inhibitors. Several agents targeting the vascular endothelial growth factor (VEGF) pathway (sunitinib, bevacizumab, pazopanib, axitinib) or the mammalian target of rapamycin pathway (temsirolimus, everolimus) were since then progressively approved for first-line or later-line use in the treatment of patients with advanced RCC and became the new standard of care. As a result, the survival of patients with advanced RCC has significantly improved from a median overall survival of approximately 12 months in the cytokines era to more than 26 months with first-line VEGF inhibitors. During the two last years, the treatment of advanced RCC has witnessed a second revolution with the advent of immune checkpoint inhibitors, especially agents targeting the programmed cell death-1 receptor, as well as with the advent of new generation tyrosine-kinase receptor inhibitors. This article will review the new therapeutic options available for the treatment of advanced RCC, as well as the future potential molecular targets that are currently being investigated. |
format | Online Article Text |
id | pubmed-5519813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | ESMO Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-55198132017-07-31 New treatment options for metastatic renal cell carcinoma Rodriguez-Vida, Alejo Hutson, Thomas E Bellmunt, Joaquim Strijbos, Michiel H ESMO Open Review During the last decade, the treatment of advanced or metastatic renal cell carcinoma (RCC) was revolutionised with the advent of antiangiogenic drugs and tyrosine-kinase inhibitors. Several agents targeting the vascular endothelial growth factor (VEGF) pathway (sunitinib, bevacizumab, pazopanib, axitinib) or the mammalian target of rapamycin pathway (temsirolimus, everolimus) were since then progressively approved for first-line or later-line use in the treatment of patients with advanced RCC and became the new standard of care. As a result, the survival of patients with advanced RCC has significantly improved from a median overall survival of approximately 12 months in the cytokines era to more than 26 months with first-line VEGF inhibitors. During the two last years, the treatment of advanced RCC has witnessed a second revolution with the advent of immune checkpoint inhibitors, especially agents targeting the programmed cell death-1 receptor, as well as with the advent of new generation tyrosine-kinase receptor inhibitors. This article will review the new therapeutic options available for the treatment of advanced RCC, as well as the future potential molecular targets that are currently being investigated. ESMO Open 2017-05-09 /pmc/articles/PMC5519813/ /pubmed/28761748 http://dx.doi.org/10.1136/esmoopen-2017-000185 Text en © European Society for Medical Oncology (unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Review Rodriguez-Vida, Alejo Hutson, Thomas E Bellmunt, Joaquim Strijbos, Michiel H New treatment options for metastatic renal cell carcinoma |
title | New treatment options for metastatic renal cell carcinoma |
title_full | New treatment options for metastatic renal cell carcinoma |
title_fullStr | New treatment options for metastatic renal cell carcinoma |
title_full_unstemmed | New treatment options for metastatic renal cell carcinoma |
title_short | New treatment options for metastatic renal cell carcinoma |
title_sort | new treatment options for metastatic renal cell carcinoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519813/ https://www.ncbi.nlm.nih.gov/pubmed/28761748 http://dx.doi.org/10.1136/esmoopen-2017-000185 |
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