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European Urology
Volume 56, issue 4, pages 583-752, October 2009Prostate Cancer
Castration-resistant Prostate Cancer: From New Pathophysiology to New Treatment Targets
Accepted 16 June 2009, Published online 24 June 2009, pages 594 - 605
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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.
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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