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
Main Authors: Vaselkiv, Jane B, Ceraolo, Carl, Wilson, Kathryn M, Pernar, Claire H, Rencsok, Emily M, Stopsack, Konrad H, Grob, Sydney T, Plym, Anna, Giovannucci, Edward L, Olumi, Aria F, Kibel, Adam S, Preston, Mark A, Mucci, Lorelei A
Format: Journal Article
Language:English
Published: United States 01-07-2022
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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.
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
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  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
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Volume 31
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