Battling resistance mechanisms in antihormonal prostate cancer treatment: Novel agents and combinations - Abstract

Prostate cancer (PCa) is a hormone-sensitive disease.

Androgen deprivation therapy lowers serum testosterone levels (castration) or blocks the androgen receptor (AR) ligand-binding domain. Especially in metastatic disease, hormonal therapy has been able to delay disease progression, reduce symptoms, and improve overall survival. Despite subsequent disease progression and development of castration resistance, PCa remains AR driven. Secondary hormonal treatments such as abiraterone acetate or enzalutamide have demonstrated increased overall survival. However, new resistance mechanisms to these agents have been identified, and systemic chemotherapy is still needed especially in fast-progressing castration-resistant PCa. Several promising androgen synthesis inhibitors (orteronel and galeterone), AR inhibitors (ARN-509, EPI-001, AZD3514, and ODM-201), and heat shock protein modulators (AT11387, 17-DMAG, STA-9090, and OGX-427) are currently under investigation. The wide variety in upcoming systemic agents underlines the molecular heterogeneity of castration-resistant PCa. This article reviews antihormonal therapy in PCa and resistance mechanisms and focuses on novel and upcoming agents currently in clinical testing.

Written by:
De Maeseneer DJ, Van Praet C, Lumen N, Rottey S.   Are you the author?
Department of Medical Oncology, Ghent University Hospital, Ghent, Belgium; Department of Urology, Ghent University Hospital, Ghent, Belgium.  

Reference: Urol Oncol. 2015 Feb 20. pii: S1078-1439(15)00010-1.
doi: 10.1016/j.urolonc.2015.01.008


PubMed Abstract
PMID: 25708954

UroToday.com Prostate Cancer Section

E-Newsletters

Newsletter subscription

Free Daily and Weekly newsletters offered by content of interest

The fields of GU Oncology and Urology are rapidly advancing. Sign up today for articles, videos, conference highlights and abstracts from peer-review publications by disease and condition delivered to your inbox and read on the go.

Subscribe