Literature DB >> 22129242

Testosterone in prostate cancer: the Bethesda consensus.

Bob Djavan1, James Eastham, Leonard Gomella, Bertrand Tombal, Samir Taneja, Seyed Saeid Dianat, Amir Kazzazi, Neal Shore, Per-Anders Abrahamsson, Philippa Cheetham, Judd Moul, Herbert Lepor, E David Crawford.   

Abstract

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.
© 2011 BJU INTERNATIONA.

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Year:  2011        PMID: 22129242     DOI: 10.1111/j.1464-410X.2011.10719.x

Source DB:  PubMed          Journal:  BJU Int        ISSN: 1464-4096            Impact factor:   5.588


  8 in total

Review 1.  Maximal testosterone suppression in prostate cancer--free vs total testosterone.

Authors:  Kyle O Rove; E David Crawford; Massimo Perachino; Juan Morote; Laurence Klotz; Paul H Lange; Gerald L Andriole; Alvin M Matsumoto; Samir S Taneja; Mario A Eisenberger; Leonardo O Reis
Journal:  Urology       Date:  2014-04-06       Impact factor: 2.649

2.  Effectiveness of Subcutaneously Administered Leuprolide Acetate to Achieve Low Nadir Testosterone in Prostate Cancer Patients.

Authors:  Christopher M Pieczonka; Przemyslaw Twardowski; Joseph Renzulli; Jason Hafron; Deborah M Boldt-Houle; Stuart Atkinson; Scott Eggener
Journal:  Rev Urol       Date:  2018

3.  Defining a new testosterone threshold for medical castration: Results from a prospective cohort series.

Authors:  Shawn Dason; Christopher B Allard; Justin Tong; Bobby Shayegan
Journal:  Can Urol Assoc J       Date:  2013 May-Jun       Impact factor: 1.862

4.  Inadequate testosterone suppression after medical and subsequent surgical castration in a patient with prostate cancer.

Authors:  Oskar Ragnarsson; Gudmundur Johannsson; Kjell Geterud; Par Lodding; Per Dahlqvist
Journal:  BMJ Case Rep       Date:  2013-08-13

Review 5.  Hormone naïve prostate cancer: predicting and maximizing response intervals.

Authors:  Judd W Moul
Journal:  Asian J Androl       Date:  2015 Nov-Dec       Impact factor: 3.285

6.  Intramuscular depot formulations of leuprolide acetate suppress testosterone levels below a 20 ng/dL threshold: a retrospective analysis of two Phase III studies.

Authors:  Aaron Spitz; Marc Gittelman; Lawrence I Karsh; Sanja Dragnic; Ahmed M Soliman; Aditya Lele; Damian Gruca; Michael Norton
Journal:  Res Rep Urol       Date:  2016-08-23

Review 7.  Androgen-targeted therapy in men with prostate cancer: evolving practice and future considerations.

Authors:  E David Crawford; Axel Heidenreich; Nathan Lawrentschuk; Bertrand Tombal; Antonio C L Pompeo; Arturo Mendoza-Valdes; Kurt Miller; Frans M J Debruyne; Laurence Klotz
Journal:  Prostate Cancer Prostatic Dis       Date:  2018-08-21       Impact factor: 5.554

8.  Red wine and component flavonoids inhibit UGT2B17 in vitro.

Authors:  Carl Jenkinson; Andrea Petroczi; Declan P Naughton
Journal:  Nutr J       Date:  2012-09-07       Impact factor: 3.271

  8 in total

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