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dc.contributor.authorWalsh, JS
dc.contributor.authorMarshall, H
dc.contributor.authorSmith, IL
dc.contributor.authorGreenfield, DM
dc.contributor.authorSwain, J
dc.contributor.authorBest, E
dc.contributor.authorAshton, J
dc.contributor.authorBrown, JM
dc.contributor.authorHuddart, R
dc.contributor.authorColeman, RE
dc.contributor.authorSnowden, JA
dc.contributor.authorRoss, RJ
dc.date.accessioned2020-01-06T11:40:25Z
dc.date.issued2019-11-12
dc.identifier.citationPLoS medicine, 2019, 16 (11), pp. e1002960 - ?
dc.identifier.issn1549-1676
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3479
dc.identifier.eissn1549-1676
dc.identifier.doi10.1371/journal.pmed.1002960
dc.description.abstractBACKGROUND: 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.
dc.formatElectronic-eCollection
dc.format.extente1002960 - ?
dc.languageeng
dc.language.isoeng
dc.publisherPUBLIC LIBRARY SCIENCE
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectAdipose Tissue
dc.subjectHumans
dc.subjectLeukemia
dc.subjectLymphoma
dc.subjectTesticular Neoplasms
dc.subjectTestosterone
dc.subjectDouble-Blind Method
dc.subjectPlacebo Effect
dc.subjectBody Composition
dc.subjectQuality of Life
dc.subjectAdult
dc.subjectMiddle Aged
dc.subjectMale
dc.subjectUnited Kingdom
dc.subjectCancer Survivors
dc.titleTestosterone replacement in young male cancer survivors: A 6-month double-blind randomised placebo-controlled trial.
dc.typeJournal Article
dcterms.dateAccepted2019-10-11
rioxxterms.versionofrecord10.1371/journal.pmed.1002960
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2019-11-12
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfPLoS medicine
pubs.issue11
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Clinical Academic Radiotherapy (Huddart)
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Clinical Academic Radiotherapy (Huddart)
pubs.publication-statusPublished
pubs.volume16
pubs.embargo.termsNot known
icr.researchteamClinical Academic Radiotherapy (Huddart)
dc.contributor.icrauthorHuddart, Robert


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