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Tivozanib: a novel VGFR inhibitor for kidney cancer
Treatment of kidney cancer has changed over the past 10 years with the approval of several targeted agents. These drugs are given on a long term base and toxicity is an issue for most patients. Despite improvement compared to immunotherapy, most patients will progress on these drugs. There is a need...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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AME Publishing Company
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708224/ https://www.ncbi.nlm.nih.gov/pubmed/26816733 http://dx.doi.org/10.3978/j.issn.2223-4683.2012.07.04 |
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author | Boyle, Helen |
author_facet | Boyle, Helen |
author_sort | Boyle, Helen |
collection | PubMed |
description | Treatment of kidney cancer has changed over the past 10 years with the approval of several targeted agents. These drugs are given on a long term base and toxicity is an issue for most patients. Despite improvement compared to immunotherapy, most patients will progress on these drugs. There is a need for more portent and better tolerated drugs. Tivozanib is a potent pan VEGR specific inhibitor. In this phase II trial it gave interesting results with an overall median PFS throughout the study of 11.7 months (95% CI: 8.3-14.3 months) and an overall objective response rate of 24% (95% CI: 19-30%). “Off”-target toxicity was mild. |
format | Online Article Text |
id | pubmed-4708224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-47082242016-01-26 Tivozanib: a novel VGFR inhibitor for kidney cancer Boyle, Helen Transl Androl Urol Research Highlight Treatment of kidney cancer has changed over the past 10 years with the approval of several targeted agents. These drugs are given on a long term base and toxicity is an issue for most patients. Despite improvement compared to immunotherapy, most patients will progress on these drugs. There is a need for more portent and better tolerated drugs. Tivozanib is a potent pan VEGR specific inhibitor. In this phase II trial it gave interesting results with an overall median PFS throughout the study of 11.7 months (95% CI: 8.3-14.3 months) and an overall objective response rate of 24% (95% CI: 19-30%). “Off”-target toxicity was mild. AME Publishing Company 2013-06 /pmc/articles/PMC4708224/ /pubmed/26816733 http://dx.doi.org/10.3978/j.issn.2223-4683.2012.07.04 Text en 2013 Translational Andrology and Urology. All rights reserved. |
spellingShingle | Research Highlight Boyle, Helen Tivozanib: a novel VGFR inhibitor for kidney cancer |
title | Tivozanib: a novel VGFR inhibitor for kidney cancer |
title_full | Tivozanib: a novel VGFR inhibitor for kidney cancer |
title_fullStr | Tivozanib: a novel VGFR inhibitor for kidney cancer |
title_full_unstemmed | Tivozanib: a novel VGFR inhibitor for kidney cancer |
title_short | Tivozanib: a novel VGFR inhibitor for kidney cancer |
title_sort | tivozanib: a novel vgfr inhibitor for kidney cancer |
topic | Research Highlight |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708224/ https://www.ncbi.nlm.nih.gov/pubmed/26816733 http://dx.doi.org/10.3978/j.issn.2223-4683.2012.07.04 |
work_keys_str_mv | AT boylehelen tivozanibanovelvgfrinhibitorforkidneycancer |