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Statin use and outcomes of oncological treatment for castration-resistant prostate cancer
To compare the effect of statin use in relation to castration-resistant prostate cancer (CRPC) treatment, we assessed the risk of ADT-treated PCa-patients to initiate CRPC treatment by statin use and the outcomes of CRPC treatment by statin use. Our study cohort consisted of 1169 men who participate...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620176/ https://www.ncbi.nlm.nih.gov/pubmed/37914793 http://dx.doi.org/10.1038/s41598-023-45958-8 |
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author | Peltomaa, A. I. Talala, K. Taari, K. Tammela, T. L. J. Auvinen, A. Murtola, T. J. |
author_facet | Peltomaa, A. I. Talala, K. Taari, K. Tammela, T. L. J. Auvinen, A. Murtola, T. J. |
author_sort | Peltomaa, A. I. |
collection | PubMed |
description | To compare the effect of statin use in relation to castration-resistant prostate cancer (CRPC) treatment, we assessed the risk of ADT-treated PCa-patients to initiate CRPC treatment by statin use and the outcomes of CRPC treatment by statin use. Our study cohort consisted of 1169 men who participated in the Finnish Randomized Study of Screening for Prostate Cancer (FinRSPC) and initiated androgen deprivation therapy (ADT) during the follow-up (1996–2017). Statin use was associated with slightly decreased risk of initiating CRPC treatment (HR 0.68; 95% CI 0.47–0.97) with a 5.7 years’ median follow-up until CRPC for non-users and 7.5 years for statin users. The risk of discontinuation of first or second line CRPC treatment due to inefficacy was not modified by statin use and the results remained similar in subgroup analysis assessing separately patients treated with taxans or androgen receptor signaling inhibitors. We observed an inverse association between statin use and the risk of initiation of the CRPC treatment. No beneficial risk modification by statin use during CRPC treatment was observed. These results suggest that statins might be beneficial during hormone-sensitive phase but not in the later phases of prostate cancer treatment. |
format | Online Article Text |
id | pubmed-10620176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106201762023-11-03 Statin use and outcomes of oncological treatment for castration-resistant prostate cancer Peltomaa, A. I. Talala, K. Taari, K. Tammela, T. L. J. Auvinen, A. Murtola, T. J. Sci Rep Article To compare the effect of statin use in relation to castration-resistant prostate cancer (CRPC) treatment, we assessed the risk of ADT-treated PCa-patients to initiate CRPC treatment by statin use and the outcomes of CRPC treatment by statin use. Our study cohort consisted of 1169 men who participated in the Finnish Randomized Study of Screening for Prostate Cancer (FinRSPC) and initiated androgen deprivation therapy (ADT) during the follow-up (1996–2017). Statin use was associated with slightly decreased risk of initiating CRPC treatment (HR 0.68; 95% CI 0.47–0.97) with a 5.7 years’ median follow-up until CRPC for non-users and 7.5 years for statin users. The risk of discontinuation of first or second line CRPC treatment due to inefficacy was not modified by statin use and the results remained similar in subgroup analysis assessing separately patients treated with taxans or androgen receptor signaling inhibitors. We observed an inverse association between statin use and the risk of initiation of the CRPC treatment. No beneficial risk modification by statin use during CRPC treatment was observed. These results suggest that statins might be beneficial during hormone-sensitive phase but not in the later phases of prostate cancer treatment. Nature Publishing Group UK 2023-11-01 /pmc/articles/PMC10620176/ /pubmed/37914793 http://dx.doi.org/10.1038/s41598-023-45958-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Peltomaa, A. I. Talala, K. Taari, K. Tammela, T. L. J. Auvinen, A. Murtola, T. J. Statin use and outcomes of oncological treatment for castration-resistant prostate cancer |
title | Statin use and outcomes of oncological treatment for castration-resistant prostate cancer |
title_full | Statin use and outcomes of oncological treatment for castration-resistant prostate cancer |
title_fullStr | Statin use and outcomes of oncological treatment for castration-resistant prostate cancer |
title_full_unstemmed | Statin use and outcomes of oncological treatment for castration-resistant prostate cancer |
title_short | Statin use and outcomes of oncological treatment for castration-resistant prostate cancer |
title_sort | statin use and outcomes of oncological treatment for castration-resistant prostate cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620176/ https://www.ncbi.nlm.nih.gov/pubmed/37914793 http://dx.doi.org/10.1038/s41598-023-45958-8 |
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