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PMID: 18957947 Published · ppublish English Comment Journal Article

Is abiraterone acetate well tolerated and effective in the treatment of castration-resistant prostate cancer?

Nature clinical practice. Oncology ·Vol. 6 ·No. 1 ·2009-01-00 ·Pages 12-3

Antonarakis ES, Eisenberger MA

Abstract

This Practice Point commentary discusses the findings of the first phase I trial to evaluate abiraterone acetate (an inhibitor of the androgen-regulating enzyme CYP17) in the treatment of castration-resistant prostate cancer. This open-label, dose-escalation study by Attard et al. showed that abiraterone was well tolerated but often induced a syndrome of secondary mineralocorticoid excess that improved with eplerenone (a mineralocorticoid receptor antagonist). Abiraterone is a potent suppressor of adrenal androgen synthesis, and produced lasting prostate-specific antigen responses in approximately half of the patients. A few patients had partial regression of distant metastases. Although promising, these results should be interpreted with caution owing to the small sample size and because the study was not primarily designed to examine drug efficacy. Multi-institutional, prospective trials should provide additional information on the tolerability and activity of this compound and further define the population most likely to benefit from this endocrine approach.

MeSH Terms
Androstenes Androstenols/administration & dosage Clinical Trials, Phase I as Topic Humans Male Maximum Tolerated Dose Orchiectomy Prostatic Neoplasms/drug therapy,pathology,surgery
Chemicals
Androstenes Androstenols abiraterone
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Antonarakis Emmanuel S
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins School of Medicine, 1650 Orleans Street, Baltimore, MD 21231,USA.
Eisenberger Mario A
References (4)
4 references, click to expand
  1. Chemotherapy for hormone-refractory prostate cancer: now it's a question of "when?".
    J Clin Oncol. 2005 Nov 10;23(32):8242-6 PMID: 16278479
  2. Intraprostatic androgens and androgen-regulated gene expression persist after testosterone suppression: therapeutic implications for castration-resistant prostate cancer.
    Cancer Res. 2007 May 15;67(10):5033-41 PMID: 17510436
  3. Increased metastatic lymph node 64 and CYP17 expression are associated with high stage prostate cancer.
    J Endocrinol. 2007 Jul;194(1):55-61 PMID: 17592021
  4. Phase I clinical trial of a selective inhibitor of CYP17, abiraterone acetate, confirms that castration-resistant prostate cancer commonly remains hormone driven.
    J Clin Oncol. 2008 Oct 1;26(28):4563-71 PMID: 18645193
Article Info
Journal
Nature clinical practice. Oncology
Abbr.
Nat Clin Pract Oncol
ISSN
1743-4262
Published
2009-01-00
Epub
2008-00-28
Pages
12-3
Language
English
Region
England
NLM ID
101226509
PMCID
PMC4014058
Subset
IM
Grants
NCI NIH HHS · P30 CA006973 · United States
Corrections
CommentOn
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