Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autor principal: Boyle, Helen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2013
Materias:
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
_version_ 1782409424540794880
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