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Effects of statin use on the response duration to androgen deprivation therapy in metastatic prostate cancer

PURPOSE: To determine whether statin use delays the development of castration-resistant prostate cancer (CRPC) in patients with metastatic prostate cancer treated with androgen deprivation therapy (ADT). MATERIALS AND METHODS: A total of 171 patients with metastatic prostate cancer at the time of di...

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Autores principales: Jung, Jaeyoon, Lee, Chunwoo, Lee, Chanwoo, Kwon, Taekmin, You, Dalsan, Jeong, In Gab, Hong, Jun Hyuk, Ahn, Hanjong, Kim, Choung-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Urological Association 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565897/
https://www.ncbi.nlm.nih.gov/pubmed/26366275
http://dx.doi.org/10.4111/kju.2015.56.9.630
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author Jung, Jaeyoon
Lee, Chunwoo
Lee, Chanwoo
Kwon, Taekmin
You, Dalsan
Jeong, In Gab
Hong, Jun Hyuk
Ahn, Hanjong
Kim, Choung-Soo
author_facet Jung, Jaeyoon
Lee, Chunwoo
Lee, Chanwoo
Kwon, Taekmin
You, Dalsan
Jeong, In Gab
Hong, Jun Hyuk
Ahn, Hanjong
Kim, Choung-Soo
author_sort Jung, Jaeyoon
collection PubMed
description PURPOSE: To determine whether statin use delays the development of castration-resistant prostate cancer (CRPC) in patients with metastatic prostate cancer treated with androgen deprivation therapy (ADT). MATERIALS AND METHODS: A total of 171 patients with metastatic prostate cancer at the time of diagnosis who were treated with ADT between January 1997 and December 2013 were retrospectively analyzed. The patients were classified into two groups: the nonstatin use group (A group) and the statin use group (B group). Multivariate analysis was performed on statin use and other factors considered likely to have an effect on the time to progression to CRPC. RESULTS: The mean patient age was 67.1±9.1 years, and the mean follow-up period was 52 months. The mean initial prostate-specific antigen (PSA) level was 537 ng/mL. Of the 171 patients, 125 (73%) were in group A and 46 (27%) were in group B. The time to progression to CRPC was 22.7 months in group A and 30.5 months in group B, and this difference was significant (p=0.032). Blood cholesterol and initial PSA levels did not differ significantly according to the time to progression to CRPC (p=0.288, p=0.198). Multivariate analysis using the Cox regression method showed that not having diabetes (p=0.037) and using a statin (p=0.045) significantly increased the odds ratio of a longer progression to CRPC. CONCLUSIONS: Statin use in metastatic prostate cancer patients appears to delay the progression to CRPC. Large-scale, long-term follow-up studies are needed to validate this finding.
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spelling pubmed-45658972015-09-11 Effects of statin use on the response duration to androgen deprivation therapy in metastatic prostate cancer Jung, Jaeyoon Lee, Chunwoo Lee, Chanwoo Kwon, Taekmin You, Dalsan Jeong, In Gab Hong, Jun Hyuk Ahn, Hanjong Kim, Choung-Soo Korean J Urol Original Article PURPOSE: To determine whether statin use delays the development of castration-resistant prostate cancer (CRPC) in patients with metastatic prostate cancer treated with androgen deprivation therapy (ADT). MATERIALS AND METHODS: A total of 171 patients with metastatic prostate cancer at the time of diagnosis who were treated with ADT between January 1997 and December 2013 were retrospectively analyzed. The patients were classified into two groups: the nonstatin use group (A group) and the statin use group (B group). Multivariate analysis was performed on statin use and other factors considered likely to have an effect on the time to progression to CRPC. RESULTS: The mean patient age was 67.1±9.1 years, and the mean follow-up period was 52 months. The mean initial prostate-specific antigen (PSA) level was 537 ng/mL. Of the 171 patients, 125 (73%) were in group A and 46 (27%) were in group B. The time to progression to CRPC was 22.7 months in group A and 30.5 months in group B, and this difference was significant (p=0.032). Blood cholesterol and initial PSA levels did not differ significantly according to the time to progression to CRPC (p=0.288, p=0.198). Multivariate analysis using the Cox regression method showed that not having diabetes (p=0.037) and using a statin (p=0.045) significantly increased the odds ratio of a longer progression to CRPC. CONCLUSIONS: Statin use in metastatic prostate cancer patients appears to delay the progression to CRPC. Large-scale, long-term follow-up studies are needed to validate this finding. The Korean Urological Association 2015-09 2015-09-02 /pmc/articles/PMC4565897/ /pubmed/26366275 http://dx.doi.org/10.4111/kju.2015.56.9.630 Text en © The Korean Urological Association, 2015 http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jung, Jaeyoon
Lee, Chunwoo
Lee, Chanwoo
Kwon, Taekmin
You, Dalsan
Jeong, In Gab
Hong, Jun Hyuk
Ahn, Hanjong
Kim, Choung-Soo
Effects of statin use on the response duration to androgen deprivation therapy in metastatic prostate cancer
title Effects of statin use on the response duration to androgen deprivation therapy in metastatic prostate cancer
title_full Effects of statin use on the response duration to androgen deprivation therapy in metastatic prostate cancer
title_fullStr Effects of statin use on the response duration to androgen deprivation therapy in metastatic prostate cancer
title_full_unstemmed Effects of statin use on the response duration to androgen deprivation therapy in metastatic prostate cancer
title_short Effects of statin use on the response duration to androgen deprivation therapy in metastatic prostate cancer
title_sort effects of statin use on the response duration to androgen deprivation therapy in metastatic prostate cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565897/
https://www.ncbi.nlm.nih.gov/pubmed/26366275
http://dx.doi.org/10.4111/kju.2015.56.9.630
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