European Urology

European Urology

Volume 56, issue 4, pages 583-752, October 2009

Prostate Cancer

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Castration-resistant Prostate Cancer: From New Pathophysiology to New Treatment Targets

Kim N. Chi, Anders Bjartell, David Dearnaley, Fred Saad, Fritz H. Schröder, Cora Sternberg, Bertrand Tombal, Tapio Visakorpi.

Accepted 16 June 2009, Published online 24 June 2009, pages 594 - 605


Abstract

Context

Castration-resistant prostate cancer (CRPC) refers to patients who no longer respond to surgical or medical castration. Standard treatment options are limited.

Objective

To review the concepts and rationale behind targeted agents currently in late-stage clinical testing for patients with CRPC.

Evidence acquisition

Novel targeted therapies in clinical trials were identified from registries. The MEDLINE database was searched for all relevant reports published from 1996 to October 2009. Bibliographies of the retrieved articles and major international meeting abstracts were hand-searched to identify additional studies.

Evidence synthesis

Advances in our understanding of the molecular mechanisms underlying prostate cancer (PCa) progression has translated into a variety of treatment approaches. Agents targeting androgen receptor (AR) activation and local steroidogenesis, angiogenesis, immunotherapy, apoptosis, chaperone proteins, the insulin-like growth factor (IGF) pathway, RANK-ligand, endothelin receptors, and the Src family kinases are entering or have recently completed accrual to phase 3 trials for patients with CRPC.

Conclusions

A number of new agents targeting mechanisms of PCa progression with early promising results are in clinical trials and have the potential to provide novel treatment options for CRPC in the near future.

Take Home Message

There has been an increased understanding of the mechanisms of progression for castration-resistant prostate cancer (CRPC). New therapeutic agents have entered into clinical trials that promise to significantly change our management of patients with CRPC in the near future.

Keywords: Prostate cancer, Androgens, Androgen receptor, Vascular endothelial growth factor, Immunotherapy, Apoptosis, Chaperone proteins, Clusterin, Insulin-like growth factor-1, Receptor activator of nuclear factor kappa B, Endothelin, Src kinase.


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