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Overcoming castration resistance in prostate cancer.
- Source :
-
Current opinion in urology [Curr Opin Urol] 2012 May; Vol. 22 (3), pp. 167-74. - Publication Year :
- 2012
-
Abstract
- Purpose of Review: Recent advances in our understanding of the androgen axis signaling pathway have led to the development of therapeutic strategies to overcome the state of 'castration resistance' in prostate cancer. In this review, we examine the mechanisms of castration resistance, as well as recently reported and ongoing clinical studies, which will further identify therapeutic opportunities for novel therapeutics targeting the androgen-signaling axis in advanced prostate cancer.<br />Recent Findings: As evidenced by recently reported positive phase III clinical trials, secondary hormonal agents such as abiraterone and MDV3100 may still be very effective in the treatment of castration-resistant prostate cancer, even after the use of docetaxel chemotherapy.<br />Summary: Novel agents targeting this pathway have demonstrated a proof of principle that overcoming castration resistance is possible, leading to significant changes in the landscape of treatment in this disease. The optimal combination, sequence, and pattern of use in these novel therapies will be the focus of clinical research in the near future.
- Subjects :
- Animals
Drug Design
Humans
Ligands
Male
Mutation
Prostatic Neoplasms drug therapy
Prostatic Neoplasms genetics
Prostatic Neoplasms metabolism
Prostatic Neoplasms surgery
Receptors, Androgen drug effects
Receptors, Androgen genetics
Receptors, Androgen metabolism
Signal Transduction drug effects
Treatment Failure
Androgen Antagonists therapeutic use
Antineoplastic Agents, Hormonal therapeutic use
Castration
Drug Resistance, Neoplasm
Prostatic Neoplasms therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1473-6586
- Volume :
- 22
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Current opinion in urology
- Publication Type :
- Academic Journal
- Accession number :
- 22472508
- Full Text :
- https://doi.org/10.1097/MOU.0b013e3283523b8b