| Literature DB >> 32938569 |
Sumanta K Pal1, Bernard J Escudier2, Michael B Atkins3, Thomas E Hutson4, Camillo Porta5, Elena Verzoni6, Michael N Needle7, Daniel Powers7, David F McDermott8, Brian I Rini9.
Abstract
Tivozanib is a potent and selective inhibitor of the VEGF receptor. In an open-label, randomized phase 3 trial, we compared tivozanib to sorafenib in patients with metastatic renal cell carcinoma (mRCC) who had received two or three prior therapies. We have previously reported that the study met its primary endpoint, demonstrating an improvement in progression-free survival with tivozanib versus sorafenib (5.6 mo vs 3.9 mo; hazard ratio [HR] 0.73, 95% confidence interval [CI] 0.56-0.94; p=0.016). The current report reflects the final assessment of overall survival, showing no difference between treatment with tivozanib and sorafenib (HR 0.97, 95% CI 0.75-1.24). Given its activity and distinct tolerability profile, tivozanib represents a treatment option for patients with previously treated mRCC. PATIENTEntities:
Keywords: Overall survival; Sorafenib; TIVO-3; Tivozanib; VEGF inhibitor
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Year: 2020 PMID: 32938569 DOI: 10.1016/j.eururo.2020.08.007
Source DB: PubMed Journal: Eur Urol ISSN: 0302-2838 Impact factor: 20.096