Expanding androgen- and androgen receptor signaling-directed therapies for castration-resistant prostate cancer
- PMID: 25140626
Expanding androgen- and androgen receptor signaling-directed therapies for castration-resistant prostate cancer
Abstract
The treatment landscape of castration-resistant prostate cancer (CRPC) has been dramatically changed over the past years with the approval of several new drugs for clinical use. These include androgen axis-targeted therapy and novel drugs with different mechanisms of action, including immunotherapy (sipuleucel-T), radiopharmaceuticals (radium-223), and chemotherapy (cabazitaxel). Based on the growing knowledge that the main driver for patients progressing on standard androgen deprivation therapy is persistent activation of the androgen receptor (AR) signaling axis, new drugs were developed and demonstrated significant efficacy in recent clinical trials, leading to the approval of abiraterone and enzalutamide in several countries. In this article, we review the most recent advances in AR-directed therapies for CRPC, promising new agents under development, cross-resistance, and mechanisms of resistance for the new-generation AR-targeted agents.
Comment in
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Targeting the androgen receptor signaling axis to reduce testosterone levels in prostate cancer: how low should we go?Oncology (Williston Park). 2014 Aug;28(8):700-1. Oncology (Williston Park). 2014. PMID: 25140627 No abstract available.
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The urology perspective on expanding androgen-targeted treatments for men with castration-resistant prostate cancer.Oncology (Williston Park). 2014 Aug;28(8):702-3, 722. Oncology (Williston Park). 2014. PMID: 25140628 No abstract available.
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