<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Vaselkiv JB</submitter><funding>NIDDK NIH HHS</funding><funding>NCI</funding><funding>NCI NIH HHS</funding><funding>NIH</funding><funding>Department of Defense</funding><pagination>1460-1465</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9250593</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(7)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>How 5-alpha reductase inhibitor (5-ARI) use influences prostate cancer mortality is unclear. The objective of this study was to determine whether men taking 5-ARIs with regular health care access have increased prostate cancer mortality.&lt;h4>Methods&lt;/h4>We undertook two analyses in the Health Professionals Follow-up Study examining 5-ARI use, determined by biennial questionnaires, and prostate cancer. A cohort analysis followed 38,037 cancer-free men for prostate cancer incidence from 1996 through January 2017 and mortality through January 2019. A case-only analysis followed 4,383 men with localized/locally advanced prostate cancer for mortality over a similar period. HRs and 95% confidence intervals (CI) were calculated for prostate cancer incidence and mortality.&lt;h4>Results&lt;/h4>Men using 5-ARIs underwent more PSA testing, prostate exams and biopsies. Over 20 years of follow-up, 509 men developed lethal disease (metastases or prostate cancer death). Among men initially free from prostate cancer, 5-ARI use was not associated with developing lethal disease [HR, 1.02; 95% confidence interval (CI), 0.71-1.46], but was associated with reduced rates of overall and localized disease (HR, 0.71; 0.60-0.83). Among men diagnosed with prostate cancer, there was no association between 5-ARI use and cancer-specific (HR, 0.78; 95% CI, 0.48-1.27) or overall survival (HR, 0.88; 95% CI, 0.72-1.07).&lt;h4>Conclusions&lt;/h4>Men using 5-ARIs were less likely to be diagnosed with low-risk prostate cancer, without increasing long-term risk of lethal prostate cancer or cancer-specific death after diagnosis.&lt;h4>Impact&lt;/h4>Our results provide evidence that 5-ARI use is safe with respect to prostate cancer mortality in the context of regular health care access. See related commentary by Hamilton, p. 1259.</pubmed_abstract><journal>Cancer epidemiology, biomarkers &amp; prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology</journal><pubmed_title>5-Alpha Reductase Inhibitors and Prostate Cancer Mortality among Men with Regular Access to Screening and Health Care.</pubmed_title><pmcid>PMC9250593</pmcid><funding_grant_id>U01 167552</funding_grant_id><funding_grant_id>U01 CA167552</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>W81XWH-18–1-0330</funding_grant_id><funding_grant_id>R01 DK124502</funding_grant_id><funding_grant_id>R01DK124502</funding_grant_id><funding_grant_id>T32 CA009001</funding_grant_id><funding_grant_id>W81XWH-19–1-0412</funding_grant_id><pubmed_authors>Wilson KM</pubmed_authors><pubmed_authors>Giovannucci EL</pubmed_authors><pubmed_authors>Preston MA</pubmed_authors><pubmed_authors>Pernar CH</pubmed_authors><pubmed_authors>Olumi AF</pubmed_authors><pubmed_authors>Kibel AS</pubmed_authors><pubmed_authors>Grob ST</pubmed_authors><pubmed_authors>Mucci LA</pubmed_authors><pubmed_authors>Stopsack KH</pubmed_authors><pubmed_authors>Rencsok EM</pubmed_authors><pubmed_authors>Vaselkiv JB</pubmed_authors><pubmed_authors>Ceraolo C</pubmed_authors><pubmed_authors>Plym A</pubmed_authors></additional><is_claimable>false</is_claimable><name>5-Alpha Reductase Inhibitors and Prostate Cancer Mortality among Men with Regular Access to Screening and Health Care.</name><description>&lt;h4>Background&lt;/h4>How 5-alpha reductase inhibitor (5-ARI) use influences prostate cancer mortality is unclear. The objective of this study was to determine whether men taking 5-ARIs with regular health care access have increased prostate cancer mortality.&lt;h4>Methods&lt;/h4>We undertook two analyses in the Health Professionals Follow-up Study examining 5-ARI use, determined by biennial questionnaires, and prostate cancer. A cohort analysis followed 38,037 cancer-free men for prostate cancer incidence from 1996 through January 2017 and mortality through January 2019. A case-only analysis followed 4,383 men with localized/locally advanced prostate cancer for mortality over a similar period. HRs and 95% confidence intervals (CI) were calculated for prostate cancer incidence and mortality.&lt;h4>Results&lt;/h4>Men using 5-ARIs underwent more PSA testing, prostate exams and biopsies. Over 20 years of follow-up, 509 men developed lethal disease (metastases or prostate cancer death). Among men initially free from prostate cancer, 5-ARI use was not associated with developing lethal disease [HR, 1.02; 95% confidence interval (CI), 0.71-1.46], but was associated with reduced rates of overall and localized disease (HR, 0.71; 0.60-0.83). Among men diagnosed with prostate cancer, there was no association between 5-ARI use and cancer-specific (HR, 0.78; 95% CI, 0.48-1.27) or overall survival (HR, 0.88; 95% CI, 0.72-1.07).&lt;h4>Conclusions&lt;/h4>Men using 5-ARIs were less likely to be diagnosed with low-risk prostate cancer, without increasing long-term risk of lethal prostate cancer or cancer-specific death after diagnosis.&lt;h4>Impact&lt;/h4>Our results provide evidence that 5-ARI use is safe with respect to prostate cancer mortality in the context of regular health care access. See related commentary by Hamilton, p. 1259.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-04-19T18:07:50.918Z</modification><creation>2025-04-19T18:07:50.918Z</creation></dates><accession>S-EPMC9250593</accession><cross_references><pubmed>35255119</pubmed><doi>10.1158/1055-9965.EPI-21-1234</doi><doi>10.1158/1055-9965.epi-21-1234</doi></cross_references></HashMap>