Open Access
REVIEW
GnRH antagonists in the treatment of advanced prostate cancer
Peter J. Pommerville1, Johan G. de Boer2
1
Can-Med Clinical Research Inc, Victoria, British Columbia, Canada
2
De Boer Consulting, Victoria, British Columbia, Canada
Address correspondence to Dr. Peter J. Pommerville, Can-Med
Clinical Research Inc, 330-1641 Hillside Avenue, Victoria, BC,
V8T 5G1 Canada
Canadian Journal of Urology 2010, 17(2), 5063-5070.
Abstract
Analogues of the gonadotropin releasing hormone
(GnRH) inhibit the hypothalamic-pituitary-gonadal
axis. This has provided treatment modalities for
advanced and metastatic prostate cancer. The latest
group of analogues, the GnRH antagonists, make
promising treatments available that avoid the transient
surge in testosterone that occurs with the use of GnRH
agonists. Such surges may stimulate tumor growth,
causing patients to experience new or worsening
cancer symptoms and potential serious adverse effects,
including increased bone pain, urinary retention, and
spinal cord compression and consequently delay the
therapeutic benefi ts of agonist therapy. Degarelix, an
antagonist, recently approved in the United States and
Europe, achieves faster, more profound and sustained
testosterone suppression and with fewer adverse effects
when compared with agonists and other antagonists.
This review discusses and compares the compounds
degarelix, abarelix, and cetrorelix.
Keywords
prostate cancer, GnRH antagonists, testosterone, treatment modality
Cite This Article
APA Style
Pommerville, P.J., Boer, J.G.D. (2010). GnRH antagonists in the treatment of advanced prostate cancer. Canadian Journal of Urology, 17(2), 5063–5070.
Vancouver Style
Pommerville PJ, Boer JGD. GnRH antagonists in the treatment of advanced prostate cancer. Can J Urology. 2010;17(2):5063–5070.
IEEE Style
P.J. Pommerville and J.G.D. Boer, “GnRH antagonists in the treatment of advanced prostate cancer,” Can. J. Urology, vol. 17, no. 2, pp. 5063–5070, 2010.
Copyright © 2010 The Canadian Journal of Urology.