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Sperm counts and endocrinological markers of spermatogenesis in long-term survivors of testicular cancer

BACKGROUND: The objective of this study was to assess markers of spermatogenesis in long-term survivors of testicular cancer (TC) according to treatment, and to explore correlations between the markers and associations with achieved paternity following TC treatment. METHODS: In 1191 TC survivors dia...

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Autores principales: Brydøy, M, Fosså, S D, Klepp, O, Bremnes, R M, Wist, E A, Bjøro, T, Wentzel-Larsen, T, Dahl, O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504949/
https://www.ncbi.nlm.nih.gov/pubmed/23169336
http://dx.doi.org/10.1038/bjc.2012.471
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author Brydøy, M
Fosså, S D
Klepp, O
Bremnes, R M
Wist, E A
Bjøro, T
Wentzel-Larsen, T
Dahl, O
author_facet Brydøy, M
Fosså, S D
Klepp, O
Bremnes, R M
Wist, E A
Bjøro, T
Wentzel-Larsen, T
Dahl, O
author_sort Brydøy, M
collection PubMed
description BACKGROUND: The objective of this study was to assess markers of spermatogenesis in long-term survivors of testicular cancer (TC) according to treatment, and to explore correlations between the markers and associations with achieved paternity following TC treatment. METHODS: In 1191 TC survivors diagnosed between 1980 and 1994, serum-follicle stimulating hormone (s-FSH; n=1191), s-inhibin B (n=441), and sperm counts (millions per ml; n=342) were analysed in a national follow-up study in 1998–2002. Paternity was assessed by a questionnaire. RESULTS: At median 11 years follow-up, 44% had oligo- (<15 millions per ml; 29%) or azoospermia (15%). Sperm counts and s-inhibin B were significantly lower and s-FSH was higher after chemotherapy, but not after radiotherapy (RT), when compared with surgery only. All measures were significantly more abnormal following high doses of chemotherapy (cisplatin (Cis)>850 mg, absolute cumulative dose) compared with lower doses (Cis ⩽850 mg). Sperm counts were moderately correlated with s-FSH (−0.500), s-inhibin B (0.455), and s-inhibin B : FSH ratio (−0.524; all P<0.001). All markers differed significantly between those who had achieved post-treatment fatherhood and those with unsuccessful attempts. CONCLUSION: The RT had no long-term effects on the assessed markers of spermatogenesis, whereas chemotherapy had. At present, the routine evaluation of s-inhibin B adds little in the initial fertility evaluation of TC survivors.
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spelling pubmed-35049492013-11-20 Sperm counts and endocrinological markers of spermatogenesis in long-term survivors of testicular cancer Brydøy, M Fosså, S D Klepp, O Bremnes, R M Wist, E A Bjøro, T Wentzel-Larsen, T Dahl, O Br J Cancer Clinical Study BACKGROUND: The objective of this study was to assess markers of spermatogenesis in long-term survivors of testicular cancer (TC) according to treatment, and to explore correlations between the markers and associations with achieved paternity following TC treatment. METHODS: In 1191 TC survivors diagnosed between 1980 and 1994, serum-follicle stimulating hormone (s-FSH; n=1191), s-inhibin B (n=441), and sperm counts (millions per ml; n=342) were analysed in a national follow-up study in 1998–2002. Paternity was assessed by a questionnaire. RESULTS: At median 11 years follow-up, 44% had oligo- (<15 millions per ml; 29%) or azoospermia (15%). Sperm counts and s-inhibin B were significantly lower and s-FSH was higher after chemotherapy, but not after radiotherapy (RT), when compared with surgery only. All measures were significantly more abnormal following high doses of chemotherapy (cisplatin (Cis)>850 mg, absolute cumulative dose) compared with lower doses (Cis ⩽850 mg). Sperm counts were moderately correlated with s-FSH (−0.500), s-inhibin B (0.455), and s-inhibin B : FSH ratio (−0.524; all P<0.001). All markers differed significantly between those who had achieved post-treatment fatherhood and those with unsuccessful attempts. CONCLUSION: The RT had no long-term effects on the assessed markers of spermatogenesis, whereas chemotherapy had. At present, the routine evaluation of s-inhibin B adds little in the initial fertility evaluation of TC survivors. Nature Publishing Group 2012-11-20 2012-11-20 /pmc/articles/PMC3504949/ /pubmed/23169336 http://dx.doi.org/10.1038/bjc.2012.471 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by-nc-sa/3.0/From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Clinical Study
Brydøy, M
Fosså, S D
Klepp, O
Bremnes, R M
Wist, E A
Bjøro, T
Wentzel-Larsen, T
Dahl, O
Sperm counts and endocrinological markers of spermatogenesis in long-term survivors of testicular cancer
title Sperm counts and endocrinological markers of spermatogenesis in long-term survivors of testicular cancer
title_full Sperm counts and endocrinological markers of spermatogenesis in long-term survivors of testicular cancer
title_fullStr Sperm counts and endocrinological markers of spermatogenesis in long-term survivors of testicular cancer
title_full_unstemmed Sperm counts and endocrinological markers of spermatogenesis in long-term survivors of testicular cancer
title_short Sperm counts and endocrinological markers of spermatogenesis in long-term survivors of testicular cancer
title_sort sperm counts and endocrinological markers of spermatogenesis in long-term survivors of testicular cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504949/
https://www.ncbi.nlm.nih.gov/pubmed/23169336
http://dx.doi.org/10.1038/bjc.2012.471
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