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Testosterone Replacement Therapy and Risk of Favorable and Aggressive Prostate Cancer

PURPOSE: The association between exposure to testosterone replacement therapy (TRT) and prostate cancer risk is controversial. The objective was to examine this association through nationwide, population-based registry data. METHODS: We performed a nested case-control study in the National Prostate...

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Autores principales: Loeb, Stacy, Folkvaljon, Yasin, Damber, Jan-Erik, Alukal, Joseph, Lambe, Mats, Stattin, Pär
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Clinical Oncology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455459/
https://www.ncbi.nlm.nih.gov/pubmed/28447913
http://dx.doi.org/10.1200/JCO.2016.69.5304
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author Loeb, Stacy
Folkvaljon, Yasin
Damber, Jan-Erik
Alukal, Joseph
Lambe, Mats
Stattin, Pär
author_facet Loeb, Stacy
Folkvaljon, Yasin
Damber, Jan-Erik
Alukal, Joseph
Lambe, Mats
Stattin, Pär
author_sort Loeb, Stacy
collection PubMed
description PURPOSE: The association between exposure to testosterone replacement therapy (TRT) and prostate cancer risk is controversial. The objective was to examine this association through nationwide, population-based registry data. METHODS: We performed a nested case-control study in the National Prostate Cancer Register of Sweden, which includes all 38,570 prostate cancer cases diagnosed from 2009 to 2012, and 192,838 age-matched men free of prostate cancer. Multivariable conditional logistic regression was used to examine associations between TRT and risk of prostate cancer (overall, favorable, and aggressive). RESULTS: Two hundred eighty-four patients with prostate cancer (1%) and 1,378 control cases (1%) filled prescriptions for TRT. In multivariable analysis, no association was found between TRT and overall prostate cancer risk (odds ratio [OR], 1.03; 95% CI, 0.90 to 1.17). However, patients who received TRT had more favorable-risk prostate cancer (OR, 1.35; 95% CI, 1.16 to 1.56) and a lower risk of aggressive prostate cancer (OR, 0.50; 95% CI, 0.37 to 0.67). The increase in favorable-risk prostate cancer was already observed within the first year of TRT (OR, 1.61; 95% CI, 1.10 to 2.34), whereas the lower risk of aggressive disease was observed after > 1 year of TRT (OR, 0.44; 95% CI, 0.32 to 0.61). After adjusting for previous biopsy findings as an indicator of diagnostic activity, TRT remained significantly associated with more favorable-risk prostate cancer and lower risk of aggressive prostate cancer. CONCLUSION: The early increase in favorable-risk prostate cancer among patients who received TRT suggests a detection bias, whereas the decrease in risk of aggressive prostate cancer is a novel finding that warrants further investigation.
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spelling pubmed-54554592018-03-16 Testosterone Replacement Therapy and Risk of Favorable and Aggressive Prostate Cancer Loeb, Stacy Folkvaljon, Yasin Damber, Jan-Erik Alukal, Joseph Lambe, Mats Stattin, Pär J Clin Oncol ORIGINAL REPORTS PURPOSE: The association between exposure to testosterone replacement therapy (TRT) and prostate cancer risk is controversial. The objective was to examine this association through nationwide, population-based registry data. METHODS: We performed a nested case-control study in the National Prostate Cancer Register of Sweden, which includes all 38,570 prostate cancer cases diagnosed from 2009 to 2012, and 192,838 age-matched men free of prostate cancer. Multivariable conditional logistic regression was used to examine associations between TRT and risk of prostate cancer (overall, favorable, and aggressive). RESULTS: Two hundred eighty-four patients with prostate cancer (1%) and 1,378 control cases (1%) filled prescriptions for TRT. In multivariable analysis, no association was found between TRT and overall prostate cancer risk (odds ratio [OR], 1.03; 95% CI, 0.90 to 1.17). However, patients who received TRT had more favorable-risk prostate cancer (OR, 1.35; 95% CI, 1.16 to 1.56) and a lower risk of aggressive prostate cancer (OR, 0.50; 95% CI, 0.37 to 0.67). The increase in favorable-risk prostate cancer was already observed within the first year of TRT (OR, 1.61; 95% CI, 1.10 to 2.34), whereas the lower risk of aggressive disease was observed after > 1 year of TRT (OR, 0.44; 95% CI, 0.32 to 0.61). After adjusting for previous biopsy findings as an indicator of diagnostic activity, TRT remained significantly associated with more favorable-risk prostate cancer and lower risk of aggressive prostate cancer. CONCLUSION: The early increase in favorable-risk prostate cancer among patients who received TRT suggests a detection bias, whereas the decrease in risk of aggressive prostate cancer is a novel finding that warrants further investigation. American Society of Clinical Oncology 2017-05-01 2017-03-13 /pmc/articles/PMC5455459/ /pubmed/28447913 http://dx.doi.org/10.1200/JCO.2016.69.5304 Text en © 2017 by American Society of Clinical Oncology http://creativecommons.org/licenses/by-nc-nd/4.0/ Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle ORIGINAL REPORTS
Loeb, Stacy
Folkvaljon, Yasin
Damber, Jan-Erik
Alukal, Joseph
Lambe, Mats
Stattin, Pär
Testosterone Replacement Therapy and Risk of Favorable and Aggressive Prostate Cancer
title Testosterone Replacement Therapy and Risk of Favorable and Aggressive Prostate Cancer
title_full Testosterone Replacement Therapy and Risk of Favorable and Aggressive Prostate Cancer
title_fullStr Testosterone Replacement Therapy and Risk of Favorable and Aggressive Prostate Cancer
title_full_unstemmed Testosterone Replacement Therapy and Risk of Favorable and Aggressive Prostate Cancer
title_short Testosterone Replacement Therapy and Risk of Favorable and Aggressive Prostate Cancer
title_sort testosterone replacement therapy and risk of favorable and aggressive prostate cancer
topic ORIGINAL REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455459/
https://www.ncbi.nlm.nih.gov/pubmed/28447913
http://dx.doi.org/10.1200/JCO.2016.69.5304
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