Literature DB >> 18666747

Sorafenib (BAY 43-9006): review of clinical development.

Raymond Ng1, Eric X Chen.   

Abstract

Sorafenib (BAY 43-9006) is a novel oral bis-aryl urea compound originally developed as an inhibitor to RAF kinase for its anti-proliferative property. It also inhibits receptor tyrosine kinases of multiple pro-angiogenic factors such as VEGFR-2/3, Flt-3/ and PDGFR-beta. The combination of both its anti-proliferative and anti-angiogenic properties makes sorafenib an attractive agent in cancer treatment. Phase I studies demonstrated that sorafenib was well tolerated, and the recommended phase II dose was 400 mg twice daily continuously. Common toxicities included skin toxicity (rash and hand-foot syndrome), gastrointestinal toxicities (nausea and diarrhea) and fatigue. Anti-tumor activities were observed in multiple tumors types including renal cell carcinoma and hepatocellular carcinoma. Randomized phase III studies in these tumor types are ongoing, and results are eagerly waited.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 18666747     DOI: 10.2174/157488406778249325

Source DB:  PubMed          Journal:  Curr Clin Pharmacol        ISSN: 1574-8847


  11 in total

1.  In vitro models of pancreatic cancer for translational oncology research.

Authors:  Georg Feldmann; Sherri Rauenzahn; Anirban Maitra
Journal:  Expert Opin Drug Discov       Date:  2009-04-01       Impact factor: 6.098

2.  Development and Validation of Sorafenib-eluting Microspheres to Enhance Therapeutic Efficacy of Transcatheter Arterial Chemoembolization in a Rat Model of Hepatocellular Carcinoma.

Authors:  Wooram Park; Soojeong Cho; Jingran Ji; Robert J Lewandowski; Andrew C Larson; Dong-Hyun Kim
Journal:  Radiol Imaging Cancer       Date:  2021-01-08

Review 3.  Refining the treatment of advanced nonsmall cell lung cancer.

Authors:  Shin Ogita; Antoinette J Wozniak
Journal:  Lung Cancer (Auckl)       Date:  2010-05-03

4.  Phase 1 study of sorafenib in combination with bortezomib in patients with advanced malignancies.

Authors:  Shaji K Kumar; James Jett; Randolph Marks; Ronald Richardson; Fernando Quevedo; Timothy Moynihan; Gary Croghan; Svetomir N Markovic; Keith C Bible; Rui Qin; Angelina Tan; Julian Molina; Scott H Kaufmann; Charles Erlichman; Alex A Adjei
Journal:  Invest New Drugs       Date:  2013-07-26       Impact factor: 3.850

Review 5.  Pharmacokinetic Aspects of Vascular Endothelial Growth Factor Tyrosine Kinase Inhibitors.

Authors:  Beatrix Wulkersdorfer; Markus Zeitlinger; Monika Schmid
Journal:  Clin Pharmacokinet       Date:  2016-01       Impact factor: 6.447

Review 6.  Exploiting cellular pathways to develop new treatment strategies for AML.

Authors:  Amir T Fathi; Steven Grant; Judith E Karp
Journal:  Cancer Treat Rev       Date:  2010-01-06       Impact factor: 12.111

7.  Nelfinavir induces mitochondria protection by ERK1/2-mediated mcl-1 stabilization that can be overcome by sorafenib.

Authors:  Ansgar Brüning; Petra Burger; Marianne Vogel; Andrea Gingelmaier; Klaus Friese; Alexander Burges
Journal:  Invest New Drugs       Date:  2009-06-26       Impact factor: 3.850

Review 8.  Role of DUSP1/MKP1 in tumorigenesis, tumor progression and therapy.

Authors:  Jiliang Shen; Yaping Zhang; Hong Yu; Bo Shen; Yuelong Liang; Renan Jin; Xiaolong Liu; Liang Shi; Xiujun Cai
Journal:  Cancer Med       Date:  2016-05-26       Impact factor: 4.452

9.  OSU-2S/Sorafenib Synergistic Antitumor Combination against Hepatocellular Carcinoma: The Role of PKCδ/p53.

Authors:  Hany A Omar; Mai F Tolba; Jui-Hsiang Hung; Taleb H Al-Tel
Journal:  Front Pharmacol       Date:  2016-11-30       Impact factor: 5.810

Review 10.  Inhibition of Soluble Epoxide Hydrolase for Renal Health.

Authors:  Jun-Yan Liu
Journal:  Front Pharmacol       Date:  2019-01-10       Impact factor: 5.810

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.