Literature DB >> 23190497

Novel agents, combinations and sequences for the treatment of advanced renal cell carcinoma: When is the revolution coming?

Matteo Santoni1, Mimma Rizzo, Luciano Burattini, Rossana Berardi, Giacomo Carteni, Stefano Cascinu.   

Abstract

Biological agents, such as multikinase inhibitors and mammalian target of rapamycin (mTOR) inhibitors, have replaced immunotherapy as the standard of care for metastatic renal cell carcinoma (mRCC). Several clinical trials have been performed, aimed to identify new feasible therapeutic targets. AKT, PI3K, STAT3, NOTCH-1, α5β1-integrin, CD70 and G250 are just examples of these opening frontiers. Novel agents, combination and sequences are emerging from the 887 clinical studies presently in course in mRCC to optimize patient outcomes. This report not includes studies on chemotherapy, local approaches, immunotherapy, surgical trials and other categories, but provides an update on ongoing phase I, II and III trials and preliminary results on targeted agents, used alone, in sequences or in combination for mRCC.

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Year:  2013        PMID: 23190497     DOI: 10.2174/1568009611313030009

Source DB:  PubMed          Journal:  Curr Cancer Drug Targets        ISSN: 1568-0096            Impact factor:   3.428


  5 in total

1.  Current practices in the management of adverse events associated with targeted therapies for advanced renal cell carcinoma: a national survey of oncologists.

Authors:  Janelle Nicole Ruiz; Viswanath Reddy Belum; Patricia Creel; Allen Cohn; Michael Ewer; Mario E Lacouture
Journal:  Clin Genitourin Cancer       Date:  2014-05-16       Impact factor: 2.872

2.  Temsirolimus for patients with metastatic renal cell carcinoma: outcomes in patients receiving temsirolimus within a compassionate use program in a tertiary referral center.

Authors:  Mehran Afshar; Jennifer Pascoe; Sue Whitmarsh; Nicholas James; Emilio Porfiri
Journal:  Drug Des Devel Ther       Date:  2014-12-17       Impact factor: 4.162

3.  Expression of microRNA-30c via lentivirus vector inhibits the proliferation and enhances the sensitivity of highly aggressive ccRCC Caki-1 cells to anticancer agents.

Authors:  Honglin Yang; Erlin Song; Guorong Shen; Tonghua Zhu; Tingwang Jiang; Hao Shen; Liping Niu; Biao Wang; Zhaoyang Lu; Jianping Qian
Journal:  Onco Targets Ther       Date:  2017-02-02       Impact factor: 4.147

4.  GLI1 reduces drug sensitivity by regulating cell cycle through PI3K/AKT/GSK3/CDK pathway in acute myeloid leukemia.

Authors:  Cheng Zhou; Juan Du; Liang Zhao; Wei Liu; Tianming Zhao; Hui Liang; Peng Fang; Kaixuan Zhang; Hui Zeng
Journal:  Cell Death Dis       Date:  2021-03-03       Impact factor: 8.469

Review 5.  Progress of molecular targeted therapies for advanced renal cell carcinoma.

Authors:  Alessandro Conti; Matteo Santoni; Consuelo Amantini; Luciano Burattini; Rossana Berardi; Giorgio Santoni; Stefano Cascinu; Giovanni Muzzonigro
Journal:  Biomed Res Int       Date:  2013-09-04       Impact factor: 3.411

  5 in total

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