5-Alpha Reductase Inhibitors and Prostate Cancer Mortality among Men with Regular Access to Screening and Health Care
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. We undertook two analyses in the Health Professionals Follow-u...
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Published in: | Cancer epidemiology, biomarkers & prevention Vol. 31; no. 7; pp. 1460 - 1465 |
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Abstract | 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.
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.
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).
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.
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. |
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AbstractList | BACKGROUNDHow 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. METHODSWe 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. RESULTSMen 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). CONCLUSIONSMen 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. IMPACTOur 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. 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. 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. 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). 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. 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. |
Author | Mucci, Lorelei A Preston, Mark A Stopsack, Konrad H Olumi, Aria F Ceraolo, Carl Wilson, Kathryn M Giovannucci, Edward L Grob, Sydney T Kibel, Adam S Vaselkiv, Jane B Plym, Anna Pernar, Claire H Rencsok, Emily M |
AuthorAffiliation | 4 Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA 7 Channing Division of Network Medicine, Department of Medicine, Brigham and Women’s Hospital, Boston, MA, USA 6 Division of Urology, Brigham and Women’s Hospital, Boston, MA, USA 3 Harvard-MIT Division of Health Sciences and Technology, Harvard Medical School, Boston, MA, USA 1 Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA 9 Department of Surgery, Beth Israel Deaconess Medical Center, Boston, MA, USA 8 Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA, USA 2 Boston University School of Medicine, Boston, MA, USA 5 Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden |
AuthorAffiliation_xml | – name: 2 Boston University School of Medicine, Boston, MA, USA – name: 6 Division of Urology, Brigham and Women’s Hospital, Boston, MA, USA – name: 8 Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA, USA – name: 5 Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden – name: 9 Department of Surgery, Beth Israel Deaconess Medical Center, Boston, MA, USA – name: 4 Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA – name: 3 Harvard-MIT Division of Health Sciences and Technology, Harvard Medical School, Boston, MA, USA – name: 7 Channing Division of Network Medicine, Department of Medicine, Brigham and Women’s Hospital, Boston, MA, USA – name: 1 Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA |
Author_xml | – sequence: 1 givenname: Jane B orcidid: 0000-0001-7702-9504 surname: Vaselkiv fullname: Vaselkiv, Jane B organization: Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts – sequence: 2 givenname: Carl orcidid: 0000-0002-4507-6696 surname: Ceraolo fullname: Ceraolo, Carl organization: Boston University School of Medicine, Boston, Massachusetts – sequence: 3 givenname: Kathryn M surname: Wilson fullname: Wilson, Kathryn M organization: Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts – sequence: 4 givenname: Claire H orcidid: 0000-0001-9549-5752 surname: Pernar fullname: Pernar, Claire H organization: Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts – sequence: 5 givenname: Emily M surname: Rencsok fullname: Rencsok, Emily M organization: Harvard-MIT Division of Health Sciences and Technology, Harvard Medical School, Boston, Massachusetts – sequence: 6 givenname: Konrad H orcidid: 0000-0002-0722-1311 surname: Stopsack fullname: Stopsack, Konrad H organization: Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York – sequence: 7 givenname: Sydney T surname: Grob fullname: Grob, Sydney T organization: Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts – sequence: 8 givenname: Anna orcidid: 0000-0001-6351-4744 surname: Plym fullname: Plym, Anna organization: Division of Urology, Brigham and Women's Hospital, Boston, Massachusetts – sequence: 9 givenname: Edward L surname: Giovannucci fullname: Giovannucci, Edward L organization: Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Massachusetts – sequence: 10 givenname: Aria F orcidid: 0000-0001-5356-2558 surname: Olumi fullname: Olumi, Aria F organization: Department of Surgery, Beth Israel Deaconess Medical Center, Boston, Massachusetts – sequence: 11 givenname: Adam S surname: Kibel fullname: Kibel, Adam S organization: Division of Urology, Brigham and Women's Hospital, Boston, Massachusetts – sequence: 12 givenname: Mark A surname: Preston fullname: Preston, Mark A organization: Division of Urology, Brigham and Women's Hospital, Boston, Massachusetts – sequence: 13 givenname: Lorelei A orcidid: 0000-0002-2551-4927 surname: Mucci fullname: Mucci, Lorelei A organization: Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts |
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Snippet | 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... BACKGROUNDHow 5-alpha reductase inhibitor (5-ARI) use influences prostate cancer mortality is unclear. The objective of this study was to determine whether men... |
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SubjectTerms | 5-alpha Reductase Inhibitors - therapeutic use Delivery of Health Care Early Detection of Cancer Follow-Up Studies Humans Male Medicin och hälsovetenskap Prostate - pathology Prostate-Specific Antigen Prostatic Neoplasms - pathology |
Title | 5-Alpha Reductase Inhibitors and Prostate Cancer Mortality among Men with Regular Access to Screening and Health Care |
URI | https://www.ncbi.nlm.nih.gov/pubmed/35255119 https://search.proquest.com/docview/2637320387 https://pubmed.ncbi.nlm.nih.gov/PMC9250593 http://kipublications.ki.se/Default.aspx?queryparsed=id:150168065 |
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