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Cabozantinib: an Active Novel Multikinase Inhibitor in Renal Cell Carcinoma
Clear cell renal cell carcinoma (RCC) is characterized by inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene. VHL loss drives tumor angiogenesis and accounts for the clinical activity of VEGF receptor (VEGFR) tyrosine kinase inhibitors (TKIs), the first-line standard of care for advan...
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/PMC5331092/ https://www.ncbi.nlm.nih.gov/pubmed/28247252 http://dx.doi.org/10.1007/s11912-017-0566-9 |
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author | Tannir, Nizar M. Schwab, Gisela Grünwald, Viktor |
author_facet | Tannir, Nizar M. Schwab, Gisela Grünwald, Viktor |
author_sort | Tannir, Nizar M. |
collection | PubMed |
description | Clear cell renal cell carcinoma (RCC) is characterized by inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene. VHL loss drives tumor angiogenesis and accounts for the clinical activity of VEGF receptor (VEGFR) tyrosine kinase inhibitors (TKIs), the first-line standard of care for advanced RCC. Within the last year, three new second-line treatments have received FDA approval for use after anti-angiogenic therapy: the immune checkpoint inhibitor nivolumab, the TKI cabozantinib, and the combination of the TKI lenvatinib and the mTOR inhibitor everolimus. Cabozantinib inhibits VEGFRs, MET, and AXL, kinases that promote tumorigenesis, angiogenesis, metastasis, and drug resistance. Compared with everolimus, cabozantinib has shown statistically significant improvements in the three key efficacy endpoints of overall survival, progression-free survival, and objective response rate in patients with RCC who were previously treated with a VEGFR TKI. Herein, we summarize the translational research and clinical development that led to approval of cabozantinib as second-line therapy in RCC. |
format | Online Article Text |
id | pubmed-5331092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-53310922017-03-20 Cabozantinib: an Active Novel Multikinase Inhibitor in Renal Cell Carcinoma Tannir, Nizar M. Schwab, Gisela Grünwald, Viktor Curr Oncol Rep Evolving Therapies (R Bukowski, Section Editor) Clear cell renal cell carcinoma (RCC) is characterized by inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene. VHL loss drives tumor angiogenesis and accounts for the clinical activity of VEGF receptor (VEGFR) tyrosine kinase inhibitors (TKIs), the first-line standard of care for advanced RCC. Within the last year, three new second-line treatments have received FDA approval for use after anti-angiogenic therapy: the immune checkpoint inhibitor nivolumab, the TKI cabozantinib, and the combination of the TKI lenvatinib and the mTOR inhibitor everolimus. Cabozantinib inhibits VEGFRs, MET, and AXL, kinases that promote tumorigenesis, angiogenesis, metastasis, and drug resistance. Compared with everolimus, cabozantinib has shown statistically significant improvements in the three key efficacy endpoints of overall survival, progression-free survival, and objective response rate in patients with RCC who were previously treated with a VEGFR TKI. Herein, we summarize the translational research and clinical development that led to approval of cabozantinib as second-line therapy in RCC. Springer US 2017-02-28 2017 /pmc/articles/PMC5331092/ /pubmed/28247252 http://dx.doi.org/10.1007/s11912-017-0566-9 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 | Evolving Therapies (R Bukowski, Section Editor) Tannir, Nizar M. Schwab, Gisela Grünwald, Viktor Cabozantinib: an Active Novel Multikinase Inhibitor in Renal Cell Carcinoma |
title | Cabozantinib: an Active Novel Multikinase Inhibitor in Renal Cell Carcinoma |
title_full | Cabozantinib: an Active Novel Multikinase Inhibitor in Renal Cell Carcinoma |
title_fullStr | Cabozantinib: an Active Novel Multikinase Inhibitor in Renal Cell Carcinoma |
title_full_unstemmed | Cabozantinib: an Active Novel Multikinase Inhibitor in Renal Cell Carcinoma |
title_short | Cabozantinib: an Active Novel Multikinase Inhibitor in Renal Cell Carcinoma |
title_sort | cabozantinib: an active novel multikinase inhibitor in renal cell carcinoma |
topic | Evolving Therapies (R Bukowski, Section Editor) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331092/ https://www.ncbi.nlm.nih.gov/pubmed/28247252 http://dx.doi.org/10.1007/s11912-017-0566-9 |
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