Literature DB >> 23875660

Current, new and novel therapy for castration-resistant prostate cancer.

Josep M Gaya1, Youness Ahallal, Rafael Sanchez-Salas, Eric Barret, Francois Rozet, Marc Galiano, Peter Macek, Matthieu Durand, Jennifer Cerruti, Dominique Prapotnich, Stanislas Ropert, Mostefa Bennamoun, Xavier Cathelineau.   

Abstract

Androgen deprivation therapy is the standard of care for the initial treatment of metastatic prostate cancer. However, the majority of these patients live long enough to experience disease progression despite castration. This scenario is defined as castration-resistant prostate cancer (CRPC) and has a poor outcome and limited options for treatment. First-line treatment after hormonal therapy failure include secondary hormonal manipulation and docetaxel. Advances in the understanding of the molecular mechanisms underlying CRPC have translated into a recent increase in the number of effective systemic agents, and some of them have been already approved as first and second-line treatment. Despite these advances, the median survival in the first-line setting of metastatic CRPC is approximately 20 months and in the postdocetaxel setting is approximately 15 months. Promising and necessary new therapies in Phase III trials include hormonal agents, new cytotoxics agents, as well as other immunotherapeutics and antiprostate-specific membrane antigen therapies.

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Year:  2013        PMID: 23875660     DOI: 10.1586/14737140.2013.811154

Source DB:  PubMed          Journal:  Expert Rev Anticancer Ther        ISSN: 1473-7140            Impact factor:   4.512


  2 in total

1.  Intensified antineoplastic effect by combining an HDAC-inhibitor, an mTOR-inhibitor and low dosed interferon alpha in prostate cancer cells.

Authors:  Igor Tsaur; Lukasz Hudak; Jasmina Makarević; Eva Juengel; Jens Mani; Hendrik Borgmann; Kilian M Gust; David Schilling; Georg Bartsch; Karen Nelson; Axel Haferkamp; Roman A Blaheta
Journal:  J Cell Mol Med       Date:  2015-03-26       Impact factor: 5.310

2.  Tumor-treating fields in combination with sorafenib curtails the growth of colorectal carcinoma by inactivating AKT/STAT3 signaling.

Authors:  Eun Ho Kim; Won Seok Lee; Hoon-Kyu Oh
Journal:  Transl Cancer Res       Date:  2022-08       Impact factor: 0.496

  2 in total

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