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Reporting and ideal testosterone levels in men undergoing androgen deprivation for prostate cancer—time for a rethink?
BACKGROUND: This study aims to review current laboratory reporting strategies across Australia and New Zealand with a view to propose a more useful template for reporting serum testosterone in the context of prostate cancer. MATERIALS AND METHODS: Registered pathology laboratories in Australia and N...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Asian Pacific Prostate Society
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857188/ https://www.ncbi.nlm.nih.gov/pubmed/29556482 http://dx.doi.org/10.1016/j.prnil.2017.05.003 |
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author | Cabarkapa, Sonja Perera, Marlon Sikaris, Ken O’Brien, Jonathan S. Bolton, Damien M. Lawrentschuk, Nathan |
author_facet | Cabarkapa, Sonja Perera, Marlon Sikaris, Ken O’Brien, Jonathan S. Bolton, Damien M. Lawrentschuk, Nathan |
author_sort | Cabarkapa, Sonja |
collection | PubMed |
description | BACKGROUND: This study aims to review current laboratory reporting strategies across Australia and New Zealand with a view to propose a more useful template for reporting serum testosterone in the context of prostate cancer. MATERIALS AND METHODS: Registered pathology laboratories in Australia and New Zealand were enrolled into the current study. An electronic or a phone survey was utilized to collect data from each participating laboratory. Obtained information included assay utilized, units reported, reference intervals, lowest reported value, and lowest detectable value. To identify recommendations for testosterone testing, a systematic search was performed across Web of Science (including MEDLINE), EMBASE, and Cochrane libraries. RESULTS: Assessment of national pathology laboratories identified significant heterogeneity in the reporting methods. Reports typically used a “normal healthy male of 35 years of age” as a comparator but did not refer to optimal castrate levels, the lowest level that their assay was able to detect, nor did they include appended clinical guidelines relating to the prostate cancer patient cohort. CONCLUSIONS: Across Australia and New Zealand, various methods for testing and reporting serum testosterone exist, while international guidelines remain vague. The fashion in which serum testosterone levels are displayed should be re-evaluated to address the relevant clinical population and reflect an agreed-upon castrate threshold in patients undergoing androgen deprivation therapy. |
format | Online Article Text |
id | pubmed-5857188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Asian Pacific Prostate Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-58571882018-03-19 Reporting and ideal testosterone levels in men undergoing androgen deprivation for prostate cancer—time for a rethink? Cabarkapa, Sonja Perera, Marlon Sikaris, Ken O’Brien, Jonathan S. Bolton, Damien M. Lawrentschuk, Nathan Prostate Int Review Article BACKGROUND: This study aims to review current laboratory reporting strategies across Australia and New Zealand with a view to propose a more useful template for reporting serum testosterone in the context of prostate cancer. MATERIALS AND METHODS: Registered pathology laboratories in Australia and New Zealand were enrolled into the current study. An electronic or a phone survey was utilized to collect data from each participating laboratory. Obtained information included assay utilized, units reported, reference intervals, lowest reported value, and lowest detectable value. To identify recommendations for testosterone testing, a systematic search was performed across Web of Science (including MEDLINE), EMBASE, and Cochrane libraries. RESULTS: Assessment of national pathology laboratories identified significant heterogeneity in the reporting methods. Reports typically used a “normal healthy male of 35 years of age” as a comparator but did not refer to optimal castrate levels, the lowest level that their assay was able to detect, nor did they include appended clinical guidelines relating to the prostate cancer patient cohort. CONCLUSIONS: Across Australia and New Zealand, various methods for testing and reporting serum testosterone exist, while international guidelines remain vague. The fashion in which serum testosterone levels are displayed should be re-evaluated to address the relevant clinical population and reflect an agreed-upon castrate threshold in patients undergoing androgen deprivation therapy. Asian Pacific Prostate Society 2018-03 2017-06-20 /pmc/articles/PMC5857188/ /pubmed/29556482 http://dx.doi.org/10.1016/j.prnil.2017.05.003 Text en © 2017 Asian Pacific Prostate Society, Published by Elsevier Korea LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Article Cabarkapa, Sonja Perera, Marlon Sikaris, Ken O’Brien, Jonathan S. Bolton, Damien M. Lawrentschuk, Nathan Reporting and ideal testosterone levels in men undergoing androgen deprivation for prostate cancer—time for a rethink? |
title | Reporting and ideal testosterone levels in men undergoing androgen deprivation for prostate cancer—time for a rethink? |
title_full | Reporting and ideal testosterone levels in men undergoing androgen deprivation for prostate cancer—time for a rethink? |
title_fullStr | Reporting and ideal testosterone levels in men undergoing androgen deprivation for prostate cancer—time for a rethink? |
title_full_unstemmed | Reporting and ideal testosterone levels in men undergoing androgen deprivation for prostate cancer—time for a rethink? |
title_short | Reporting and ideal testosterone levels in men undergoing androgen deprivation for prostate cancer—time for a rethink? |
title_sort | reporting and ideal testosterone levels in men undergoing androgen deprivation for prostate cancer—time for a rethink? |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857188/ https://www.ncbi.nlm.nih.gov/pubmed/29556482 http://dx.doi.org/10.1016/j.prnil.2017.05.003 |
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