Literature DB >> 21732754

Ridaforolimus: a promising drug in the treatment of soft-tissue sarcoma and other malignancies.

Janet E Dancey1, Jose Monzon.   

Abstract

Ridaforolimus (deforolimus; AP23573; MK-8669) is a novel sirolimus derivative manufactured by ARIAD Pharmaceuticals and acquired by Merck. It is a small-molecule kinase inhibitor of the mTOR in clinical development for the treatment of cancer. Both intravenous and oral formulations of the agent are being tested in cancer clinical trials. In preclinical and clinical studies, ridaforolimus exhibited significant antitumor activity with acceptable safety and tolerability. With single-agent ridaforolimus, mucositis and myelosuppression were dose-limiting toxicities. In advanced soft-tissue sarcoma, single-agent ridaforolimus was associated with a 29% clinical benefit rate and 2% partial response rate. A Phase III trial has recently been reported to have met its primary end point.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21732754     DOI: 10.2217/fon.11.57

Source DB:  PubMed          Journal:  Future Oncol        ISSN: 1479-6694            Impact factor:   3.404


  13 in total

Review 1.  Differentiating mTOR inhibitors in renal cell carcinoma.

Authors:  Sumanta K Pal; David I Quinn
Journal:  Cancer Treat Rev       Date:  2013-02-21       Impact factor: 12.111

Review 2.  Novel and emerging targeted-based cancer therapy agents and methods.

Authors:  Mohammad Hojjat-Farsangi
Journal:  Tumour Biol       Date:  2015-02-09

Review 3.  Targeting the PI3K pathway for cancer therapy.

Authors:  Navid Sadeghi; David E Gerber
Journal:  Future Med Chem       Date:  2012-06       Impact factor: 3.808

Review 4.  Applying what we know to accelerate cancer prevention.

Authors:  Graham A Colditz; Kathleen Y Wolin; Sarah Gehlert
Journal:  Sci Transl Med       Date:  2012-03-28       Impact factor: 17.956

5.  Results of a phase 1 trial combining ridaforolimus and MK-0752 in patients with advanced solid tumours.

Authors:  S A Piha-Paul; P N Munster; A Hollebecque; G Argilés; O Dajani; J D Cheng; R Wang; A Swift; A Tosolini; S Gupta
Journal:  Eur J Cancer       Date:  2015-07-18       Impact factor: 9.162

6.  A prospective observational study on the evaluation of everolimus-related adverse events in metastatic renal cell carcinoma after first-line anti-vascular endothelial growth factor therapy: the AFINITE study in France.

Authors:  Florence Joly; Jean-Christophe Eymard; Laurence Albiges; Thierry Nguyen; Aline Guillot; Frederic Rolland; Dominique Spaeth; Brigitte Laguerre; Thierry Lebret; Nadia Kelkouli; Khemaies Slimane; Alain Ravaud
Journal:  Support Care Cancer       Date:  2017-02-10       Impact factor: 3.603

7.  A single supratherapeutic dose of ridaforolimus does not prolong the QTc interval in patients with advanced cancer.

Authors:  Richard M Lush; Amita Patnaik; Daniel Sullivan; Kyriakos P Papadopoulos; Michele Trucksis; Jacqueline McCrea; Kristine Cerchio; Xiaodong Li; Mark Stroh; Diana Selverian; Keith Orford; Scot Ebbinghaus; Nancy Agrawal; Marian Iwamoto; John A Wagner; Anthony Tolcher
Journal:  Cancer Chemother Pharmacol       Date:  2012-08-10       Impact factor: 3.333

Review 8.  The mTOR signaling pathway in the brain: focus on epilepsy and epileptogenesis.

Authors:  Emilio Russo; Rita Citraro; Andrew Constanti; Giovambattista De Sarro
Journal:  Mol Neurobiol       Date:  2012-07-24       Impact factor: 5.682

Review 9.  Management of adverse events in patients with hormone receptor-positive breast cancer treated with everolimus: observations from a phase III clinical trial.

Authors:  Mary E Peterson
Journal:  Support Care Cancer       Date:  2013-05-19       Impact factor: 3.603

10.  Ridaforolimus as a single agent in advanced endometrial cancer: results of a single-arm, phase 2 trial.

Authors:  N Colombo; D S McMeekin; P E Schwartz; C Sessa; P A Gehrig; R Holloway; P Braly; D Matei; A Morosky; P F Dodion; M H Einstein; F Haluska
Journal:  Br J Cancer       Date:  2013-02-12       Impact factor: 7.640

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.