Skip to main content
Journal cover image

Testosterone in prostate cancer: the Bethesda consensus.

Publication ,  Journal Article
Djavan, B; Eastham, J; Gomella, L; Tombal, B; Taneja, S; Dianat, SS; Kazzazi, A; Shore, N; Abrahamsson, P-A; Cheetham, P; Moul, J; Lepor, H ...
Published in: BJU Int
August 2012

OBJECTIVE: • Androgen stimulation of prostate cancer (PCa) cells has been extensively studied. The increasing trend of using serum testosterone as an absolute surrogate for castration state means that the diagnostic measurement of testosterone and the values potentially influencing prognosis must be better understood. This is especially important when PCa progresses from an endocrine to an intracrine status. PATIENTS AND METHODS: • We performed a literature review using the MEDLINE database for publications on: (i) hormonal changes with androgen deprivation therapy (ADT); (ii) monitoring hormonal therapy with testosterone measurement; (iii) the efficacy of intermittent androgen deprivation (IAD) compared with continuous androgen deprivation; (iv) the underlying mechanisms of castration-resistance; and (v) novel treatments for castration-resistant PCa (CRPCa). RESULTS: • The optimum serum castration levels to be achieved with ADT are still debated. Recently, the 50 ng/dL threshold has been questioned because of reports indicating worse outcomes when levels between 20 and 50 ng/dL were studied. Instead, a 20 ng/dL threshold for serum testosterone after ADT in patients with advanced prostate cancer was recommended. CONCLUSION: • Understanding the mechanisms of androgen biosynthesis relating to PCa as well as prognostic implications might achieve a consensus regarding the role of ADT for both the androgen-sensitive and -insensitive disease state.

Duke Scholars

Altmetric Attention Stats
Dimensions Citation Stats

Published In

BJU Int

DOI

EISSN

1464-410X

Publication Date

August 2012

Volume

110

Issue

3

Start / End Page

344 / 352

Location

England

Related Subject Headings

  • Urology & Nephrology
  • Therapies, Investigational
  • Testosterone
  • Proto-Oncogene Proteins c-bcl-2
  • Prostatic Neoplasms
  • Prognosis
  • Practice Guidelines as Topic
  • Orchiectomy
  • Neoplastic Stem Cells
  • Metabolic Networks and Pathways
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Djavan, B., Eastham, J., Gomella, L., Tombal, B., Taneja, S., Dianat, S. S., … Crawford, E. D. (2012). Testosterone in prostate cancer: the Bethesda consensus. BJU Int, 110(3), 344–352. https://doi.org/10.1111/j.1464-410X.2011.10719.x
Djavan, Bob, James Eastham, Leonard Gomella, Bertrand Tombal, Samir Taneja, Seyed Saeid Dianat, Amir Kazzazi, et al. “Testosterone in prostate cancer: the Bethesda consensus.BJU Int 110, no. 3 (August 2012): 344–52. https://doi.org/10.1111/j.1464-410X.2011.10719.x.
Djavan B, Eastham J, Gomella L, Tombal B, Taneja S, Dianat SS, et al. Testosterone in prostate cancer: the Bethesda consensus. BJU Int. 2012 Aug;110(3):344–52.
Djavan, Bob, et al. “Testosterone in prostate cancer: the Bethesda consensus.BJU Int, vol. 110, no. 3, Aug. 2012, pp. 344–52. Pubmed, doi:10.1111/j.1464-410X.2011.10719.x.
Djavan B, Eastham J, Gomella L, Tombal B, Taneja S, Dianat SS, Kazzazi A, Shore N, Abrahamsson P-A, Cheetham P, Moul J, Lepor H, Crawford ED. Testosterone in prostate cancer: the Bethesda consensus. BJU Int. 2012 Aug;110(3):344–352.
Journal cover image

Published In

BJU Int

DOI

EISSN

1464-410X

Publication Date

August 2012

Volume

110

Issue

3

Start / End Page

344 / 352

Location

England

Related Subject Headings

  • Urology & Nephrology
  • Therapies, Investigational
  • Testosterone
  • Proto-Oncogene Proteins c-bcl-2
  • Prostatic Neoplasms
  • Prognosis
  • Practice Guidelines as Topic
  • Orchiectomy
  • Neoplastic Stem Cells
  • Metabolic Networks and Pathways