Evidence map›Paper›PMID 30216624›Full record

ArticleBJU international2019

Impact of 5α-reductase inhibitor and α-blocker therapy for benign prostatic hyperplasia on prostate cancer incidence and mortality.

Maria I Van Rompay, J Curtis Nickel, Gayatri Ranganathan, Philip W Kantoff, Keith R Solomon, Jennifer L Lund, John B McKinlay

Abstract read
In one paragraph

Article in BJU international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 6 institutions in 2 countries.

Maria I Van RompayHealthCore-NERI, Watertown, MA, USA.ORCID 0000-0002-4878-0881
J Curtis NickelKingston General Hospital, Queen's University, Kingston, ON, Canada.
Gayatri RanganathanHealthCore-NERI, Watertown, MA, USA.
Philip W KantoffMemorial Sloan Kettering Cancer Center, Weill Cornell Medical College, New York, NY, USA.
Keith R SolomonDepartment of Orthopaedic Surgery, Harvard Medical School, Boston, MA, USA.
Jennifer L LundDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
John B McKinlayHealthCore-NERI, Watertown, MA, USA.
New England Research Institutes · USBoston Children's Hospital · USHarvard University · USMemorial Sloan Kettering Cancer Center · USQueen's University · CAUniversity of North Carolina at Chapel Hill · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Chemoprevention of Prostate CancerR01AG038453 · NIA · NEW ENGLAND RESEARCH INSTITUTES, INC. · PI VAN ROMPAY, MARIA IRENE · 2011 to 2014
$623k
NCI NIH HHS P30 CA008748NIA NIH HHS R01 AG038453
6 · The paper itself

Abstract

objectiveTo investigate the use of 5α-reductase inhibitors (5ARIs) and α-blockers among men with benign prostatic hyperplasia (BPH) in relation to prostate cancer (PCa) incidence, severity and mortality. PATIENTS AND

methodsA retrospective 20-year cohort study in men residing in Saskatchewan, aged 40-89 years, with a BPH-coded medical claim between 1995 and 2014, was conducted. Cox proportional hazards regression was used to compare incidence of PCa diagnosis, metastatic PCa, Gleason score 8-10 PCa, and PCa mortality among 5ARI users (n = 4 571), α-blocker users (n = 7 764) and non-users (n = 11 677).

resultsIn comparison with both non-users and α-blocker users, 5ARI users had a ~40% lower risk of a PCa diagnosis (11.0% and 11.4% vs 5.8%, respectively), and α-blocker users had an 11% lower risk of a PCa diagnosis compared with non-users. Overall, the incidence of metastatic PCa and PCa mortality was not significantly different among 5ARI or α-blocker users compared with non-users (adjusted hazard ratios [HR] of metastatic PCa: 1.12 and 1.13, respectively, and PCa mortality: 1.11 and 1.18, respectively, P > 0.05 for both drugs), but both 5ARI and a-blocker users had ~30% higher risk of Gleason score 8-10 cancer, adjusted HR 1.37, 95% confidence interval [CI] 1.03-1.82, P = 0.03, and adjusted HR 1.28, 95% CI 1.03-1.59, P = 0.02, respectively compared with non-users.

conclusionThe use of 5ARIs was associated with lower risk of PCa diagnosis, regardless of comparison group. Risk of high grade PCa was higher among both 5ARI users and α-blocker users compared with non-users; however, this did not translate into higher risk of PCa mortality.

Indexed as

5-alpha Reductase InhibitorsAdrenergic alpha-AntagonistsAdultAgedAged, 80 and overDisease ProgressionDrug Therapy, CombinationHumansIncidenceMaleMiddle AgedProportional Hazards ModelsProstatic HyperplasiaProstatic NeoplasmsRetrospective StudiesSaskatchewan5-alpha Reductase InhibitorsAdrenergic alpha-Antagonistsadrenergic alpha-antagonistsbenign prostatic hyperplasiadutasteridefinasteridepharmacoepidemiology#ProstateCancerprostatic neoplasms

Identifiers

PMID30216624
PMCPMC6397052
OpenAlexW2890743632

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.