Testosterone replacement therapy (TRT) and prostate cancer: An updated systematic review with a focus on previous or active localized prostate cancer.

Androgen Hypogonadism Prostate cancer Testosterone deficiency Testosterone therapy Therapeutics

Journal

Urologic oncology
ISSN: 1873-2496
Titre abrégé: Urol Oncol
Pays: United States
ID NLM: 9805460

Informations de publication

Date de publication:
08 2020
Historique:
received: 19 12 2019
revised: 06 04 2020
accepted: 10 04 2020
pubmed: 16 5 2020
medline: 30 4 2021
entrez: 16 5 2020
Statut: ppublish

Résumé

Often contraindicated because of the theoretical risk of progression based on the dogma of hormone dependent prostate cancer (CaP), testosterone replacement therapy (TRT) is increasingly discussed and proposed for hypogonadal patients with localized CaP. To perform a systematic literature review to determine the relationship between TRT and the risk of CaP with a focus on the impact of TRT in the setting of previous or active localized CaP. As of October 15, 2019, systematic review was performed via Medline Embase and Cochrane databases in accordance with the PRISMA guidelines. All full text articles in English published from January 1994 to February 2018 were included. Articles were considered if they reported about the relationship between total testosterone or bioavailable testosterone and CaP. Emphasis was given to prospective studies, series with observational data and randomized controlled trials. Articles about the safety of the testosterone therapy were categorized by type of CaP management (active surveillance or curative treatment by radical prostatectomy, external radiotherapy or brachytherapy). Until more definitive data becomes available, clinicians wishing to treat their hypogonadal patients with localized CaP with TRT should inform them of the lack of evidence regarding the safety of long-term treatment for the risk of CaP progression. However, in patients without known CaP, the evidence seems sufficient to think that androgen therapy does not increase the risk of subsequent discovery of CaP.

Identifiants

pubmed: 32409202
pii: S1078-1439(20)30151-4
doi: 10.1016/j.urolonc.2020.04.008
pii:
doi:

Substances chimiques

Testosterone 3XMK78S47O

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

661-670

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Louis Lenfant (L)

Urology department, Sorbonne University, GRC n 5, PREDICTIVE ONCO-UROLOGY, AP-HP, Hôpital Pitié-Salpêtrière, Paris, France. Electronic address: louis.lenfant@aphp.fr.

Priscilla Leon (P)

Service d'urologie, Clinique Pasteur, Royan, France; GRC n 5 PREDICTIVE ONCO-UROLOGY, Sorbonne Université, AP-HP, Hôpital Tenon, Paris, France.

Géraldine Cancel-Tassin (G)

GRC n 5 PREDICTIVE ONCO-UROLOGY, Sorbonne Université, AP-HP, Hôpital Tenon, Paris, France; CeRePP, Paris, France.

Marie Audouin (M)

GRC n 5 PREDICTIVE ONCO-UROLOGY, Sorbonne Université, AP-HP, Hôpital Tenon, Paris, France.

Frédéric Staerman (F)

Service d'urologie et d'andrologie de la polyclinique de Reims - Bezannes, Reims, France.

Morgan Rouprêt (M)

GRC n 5 PREDICTIVE ONCO-UROLOGY, Sorbonne Université, AP-HP, Hôpital Tenon, Paris, France; CeRePP, Paris, France; Urology department, Sorbonne University, GRC n 5, PREDICTIVE ONCO-UROLOGY, AP-HP, Hôpital Pitié-Salpêtrière, Paris, France.

Olivier Cussenot (O)

GRC n 5 PREDICTIVE ONCO-UROLOGY, Sorbonne Université, AP-HP, Hôpital Tenon, Paris, France; CeRePP, Paris, France.

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