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Testosterone replacement in young male cancer survivors: A 6-month double-blind randomised placebo-controlled trial

BACKGROUND: Young male cancer survivors have lower testosterone levels, higher fat mass, and worse quality of life (QoL) than age-matched healthy controls. Low testosterone in cancer survivors can be due to orchidectomy or effects of chemotherapy and radiotherapy. We have undertaken a double-blind,...

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Autores principales: Walsh, Jennifer S., Marshall, Helen, Smith, Isabelle L., Greenfield, Diana M., Swain, Jayne, Best, Emma, Ashton, James, Brown, Julia M., Huddart, Robert, Coleman, Robert E., Snowden, John A., Ross, Richard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850530/
https://www.ncbi.nlm.nih.gov/pubmed/31714912
http://dx.doi.org/10.1371/journal.pmed.1002960
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author Walsh, Jennifer S.
Marshall, Helen
Smith, Isabelle L.
Greenfield, Diana M.
Swain, Jayne
Best, Emma
Ashton, James
Brown, Julia M.
Huddart, Robert
Coleman, Robert E.
Snowden, John A.
Ross, Richard J.
author_facet Walsh, Jennifer S.
Marshall, Helen
Smith, Isabelle L.
Greenfield, Diana M.
Swain, Jayne
Best, Emma
Ashton, James
Brown, Julia M.
Huddart, Robert
Coleman, Robert E.
Snowden, John A.
Ross, Richard J.
author_sort Walsh, Jennifer S.
collection PubMed
description BACKGROUND: Young male cancer survivors have lower testosterone levels, higher fat mass, and worse quality of life (QoL) than age-matched healthy controls. Low testosterone in cancer survivors can be due to orchidectomy or effects of chemotherapy and radiotherapy. We have undertaken a double-blind, placebo-controlled, 6-month trial of testosterone replacement in young male cancer survivors with borderline low testosterone (7–12 nmol/l). METHODS AND FINDINGS: This was a multicentre United Kingdom study conducted in secondary care hospital outpatients. Male survivors of testicular cancer, lymphoma, and leukaemia aged 25–50 years with morning total serum testosterone 7–12 nmol/l were recruited. A total of 136 men were randomised between July 2012 and February 2015 (42.6% aged 25–37 years, 57.4% 38–50 years, 88% testicular cancer, 10% lymphoma, matched for body mass index [BMI]). Participants were randomised 1:1 to receive testosterone (Tostran 2% gel) or placebo for 26 weeks. A dose titration was performed after 2 weeks. The coprimary end points were trunk fat mass and SF36 Physical Functioning score (SF36-PF) at 26 weeks by intention to treat. At 26 weeks, testosterone treatment compared with placebo was associated with decreased trunk fat mass (−0.9 kg, 95% CI −1.6 to −0.3, p = 0.0073), decreased whole-body fat mass (−1.8 kg, 95% CI −2.9 to −0.7, p = 0.0016), and increased lean body mass (1.5 kg, 95% CI 0.9–2.1, p < 0.001). Decrease in fat mass was greatest in those with a high truncal fat mass at baseline. There was no treatment effect on SF36-PF or any other QoL scores. Testosterone treatment was well tolerated. The limitations of our study were as follows: a relatively short duration of treatment, only three cancer groups included, and no hard end point data such as cardiovascular events. CONCLUSIONS: In young male cancer survivors with low-normal morning total serum testosterone, replacement with testosterone is associated with an improvement in body composition. TRIAL REGISTRATION: ISRCTN: 70274195, EudraCT: 2011-000677-31.
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spelling pubmed-68505302019-11-22 Testosterone replacement in young male cancer survivors: A 6-month double-blind randomised placebo-controlled trial Walsh, Jennifer S. Marshall, Helen Smith, Isabelle L. Greenfield, Diana M. Swain, Jayne Best, Emma Ashton, James Brown, Julia M. Huddart, Robert Coleman, Robert E. Snowden, John A. Ross, Richard J. PLoS Med Research Article BACKGROUND: Young male cancer survivors have lower testosterone levels, higher fat mass, and worse quality of life (QoL) than age-matched healthy controls. Low testosterone in cancer survivors can be due to orchidectomy or effects of chemotherapy and radiotherapy. We have undertaken a double-blind, placebo-controlled, 6-month trial of testosterone replacement in young male cancer survivors with borderline low testosterone (7–12 nmol/l). METHODS AND FINDINGS: This was a multicentre United Kingdom study conducted in secondary care hospital outpatients. Male survivors of testicular cancer, lymphoma, and leukaemia aged 25–50 years with morning total serum testosterone 7–12 nmol/l were recruited. A total of 136 men were randomised between July 2012 and February 2015 (42.6% aged 25–37 years, 57.4% 38–50 years, 88% testicular cancer, 10% lymphoma, matched for body mass index [BMI]). Participants were randomised 1:1 to receive testosterone (Tostran 2% gel) or placebo for 26 weeks. A dose titration was performed after 2 weeks. The coprimary end points were trunk fat mass and SF36 Physical Functioning score (SF36-PF) at 26 weeks by intention to treat. At 26 weeks, testosterone treatment compared with placebo was associated with decreased trunk fat mass (−0.9 kg, 95% CI −1.6 to −0.3, p = 0.0073), decreased whole-body fat mass (−1.8 kg, 95% CI −2.9 to −0.7, p = 0.0016), and increased lean body mass (1.5 kg, 95% CI 0.9–2.1, p < 0.001). Decrease in fat mass was greatest in those with a high truncal fat mass at baseline. There was no treatment effect on SF36-PF or any other QoL scores. Testosterone treatment was well tolerated. The limitations of our study were as follows: a relatively short duration of treatment, only three cancer groups included, and no hard end point data such as cardiovascular events. CONCLUSIONS: In young male cancer survivors with low-normal morning total serum testosterone, replacement with testosterone is associated with an improvement in body composition. TRIAL REGISTRATION: ISRCTN: 70274195, EudraCT: 2011-000677-31. Public Library of Science 2019-11-12 /pmc/articles/PMC6850530/ /pubmed/31714912 http://dx.doi.org/10.1371/journal.pmed.1002960 Text en © 2019 Walsh et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Walsh, Jennifer S.
Marshall, Helen
Smith, Isabelle L.
Greenfield, Diana M.
Swain, Jayne
Best, Emma
Ashton, James
Brown, Julia M.
Huddart, Robert
Coleman, Robert E.
Snowden, John A.
Ross, Richard J.
Testosterone replacement in young male cancer survivors: A 6-month double-blind randomised placebo-controlled trial
title Testosterone replacement in young male cancer survivors: A 6-month double-blind randomised placebo-controlled trial
title_full Testosterone replacement in young male cancer survivors: A 6-month double-blind randomised placebo-controlled trial
title_fullStr Testosterone replacement in young male cancer survivors: A 6-month double-blind randomised placebo-controlled trial
title_full_unstemmed Testosterone replacement in young male cancer survivors: A 6-month double-blind randomised placebo-controlled trial
title_short Testosterone replacement in young male cancer survivors: A 6-month double-blind randomised placebo-controlled trial
title_sort testosterone replacement in young male cancer survivors: a 6-month double-blind randomised placebo-controlled trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850530/
https://www.ncbi.nlm.nih.gov/pubmed/31714912
http://dx.doi.org/10.1371/journal.pmed.1002960
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