Literature DB >> 24756792

Regorafenib.

Thomas J Ettrich1, Thomas Seufferlein.   

Abstract

Regorafenib (BAY 73-4506, Stivarga®) is an oral diphenylurea multikinase inhibitor that targets angiogenic (VEGFR1-3, TIE2), stromal (PDGFR-β, FGFR), and oncogenic receptor tyrosine kinases (KIT, RET, and RAF). Regorafenib is the first small-molecule multikinase inhibitor to achieve survival benefits in metastatic colorectal cancer that has progressed after all standard therapies. Consequently, regorafenib was FDA approved for this indication. In addition, regorafenib treatment resulted in a significant improvement in progression-free survival (PFS) compared with placebo in patients with metastatic gastrointestinal stromal tumors (GIST) after progression on standard treatments and is also an FDA approved indication. Currently, regorafenib is examined in several clinical trials (mostly phase II) in different tumor entities, including renal cell carcinoma (RCC), hepatocellular carcinoma (HCC), and soft tissue sarcoma (STS).

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Year:  2014        PMID: 24756792     DOI: 10.1007/978-3-642-54490-3_10

Source DB:  PubMed          Journal:  Recent Results Cancer Res        ISSN: 0080-0015


  11 in total

Review 1.  Next-generation sequencing and personalized genomic medicine in hepatobiliary malignancies.

Authors:  Arturo Loaiza-Bonilla; Emma E Furth; Jennifer Jd Morrissette
Journal:  Hepat Oncol       Date:  2015-11-11

Review 2.  The molecular basis for RET tyrosine-kinase inhibitors in thyroid cancer.

Authors:  Valentina De Falco; Francesca Carlomagno; Hong-Yu Li; Massimo Santoro
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2017-05-10       Impact factor: 4.690

Review 3.  Therapy in Advanced Hepatocellular Carcinoma.

Authors:  Hanna Javan; Farshid Dayyani; Nadine Abi-Jaoudeh
Journal:  Semin Intervent Radiol       Date:  2020-12-11       Impact factor: 1.513

4.  Regorefenib induces extrinsic/intrinsic apoptosis and inhibits MAPK/NF-κB-modulated tumor progression in bladder cancer in vitro and in vivo.

Authors:  Chih-Hung Chiang; Jing-Gung Chung; Fei-Ting Hsu
Journal:  Environ Toxicol       Date:  2019-02-25       Impact factor: 4.119

5.  Molecular Modelling Studies on Pyrazole Derivatives for the Design of Potent Rearranged during Transfection Kinase Inhibitors.

Authors:  Swapnil P Bhujbal; Seketoulie Keretsu; Seung Joo Cho
Journal:  Molecules       Date:  2021-01-28       Impact factor: 4.411

6.  Regorafenib sensitizes human breast cancer cells to radiation by inhibiting multiple kinases and inducing DNA damage.

Authors:  Meghna Mehta; James Griffith; Janani Panneerselvam; Anish Babu; Jonathan Mani; Terence Herman; Rajagopal Ramesh; Anupama Munshi
Journal:  Int J Radiat Biol       Date:  2020-03-02       Impact factor: 2.694

7.  Resistance to multikinase inhibitor actions mediated by insulin like growth factor-1.

Authors:  Catia Lippolis; Maria Grazia Refolo; Rosalba D'Alessandro; Nicola Carella; Caterina Messa; Aldo Cavallini; Brian Irving Carr
Journal:  J Exp Clin Cancer Res       Date:  2015-09-02

8.  Anti-proliferative but not anti-angiogenic tyrosine kinase inhibitors enrich for cancer stem cells in soft tissue sarcoma.

Authors:  Robert J Canter; Erik Ames; Stephanie Mac; Steven K Grossenbacher; Mingyi Chen; Chin-Shang Li; Dariusz Borys; Rachel C Smith; Joe Tellez; Thomas J Sayers; Arta M Monjazeb; William J Murphy
Journal:  BMC Cancer       Date:  2014-10-10       Impact factor: 4.430

9.  Characterization of FGFR signaling pathway as therapeutic targets for sarcoma patients.

Authors:  Wen-Ya Zhou; Hong Zheng; Xiao-Ling Du; Ji-Long Yang
Journal:  Cancer Biol Med       Date:  2016-06       Impact factor: 4.248

Review 10.  Antisense Oligonucleotides Targeting Angiogenic Factors as Potential Cancer Therapeutics.

Authors:  Bao T Le; Prithi Raguraman; Tamer R Kosbar; Susan Fletcher; Steve D Wilton; Rakesh N Veedu
Journal:  Mol Ther Nucleic Acids       Date:  2018-11-20
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