Evidence map›Paper›PMID 39153780›Full record

ArticleBMJ open2024

How a population-based cohort of men estimate lifetime risk of prostate cancer in a survey before entering a prostate cancer screening trial in Sweden?

Emmeli Palmstedt, Marianne Månsson, Karin Stinesen Kollberg, Sigrid Carlsson, Mikael Hellström, Jonas Wallström, Jonas Hugosson, Rebecka Arnsrud Godtman

Abstract read
In one paragraph

Article in BMJ open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Emmeli PalmstedtDepartment of Urology, University of Gothenburg Institute of Clinical Sciences, Goteborg, Sweden emmeli_p@hotmail.com.ORCID 0009-0009-9219-8934
Marianne MånssonDepartment of Urology, University of Gothenburg Institute of Clinical Sciences, Goteborg, Sweden.
Karin Stinesen KollbergDepartment of Urology, University of Gothenburg Institute of Clinical Sciences, Goteborg, Sweden.
Sigrid CarlssonDepartment of Surgery and Epidemiology and Biostatistics, Memorial Sloan-Kettering Cancer Center, New York City, New York, USA.
Mikael HellströmDepartment of Radiology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Jonas WallströmDepartment of Radiology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Jonas HugossonDepartment of Urology, University of Gothenburg Institute of Clinical Sciences, Goteborg, Sweden.
Rebecka Arnsrud GodtmanDepartment of Urology, University of Gothenburg Institute of Clinical Sciences, Goteborg, Sweden.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

objectivesInvestigating men's perceived lifetime risk of prostate cancer.

designSurvey-based study to men invited for prostate-specific antigen (PSA) screening in the GÖTEBORG-2 trial between September 2015 and June 2020.

setting38 775 men in the Gothenburg area, Sweden, were invited for PSA-testing and participated in a survey.

participants17 980 men participated in PSA-testing, of whom 13 189 completed the survey. In addition, 1264 men answered the survey only.

interventionsBefore having the PSA-test, men answered an electronic survey and estimated their lifetime risk of receiving a prostate cancer diagnosis on a visual analogue scale from 0% to 100%.

main outcome measuresThe primary outcome was the median lifetime risk estimation, which was compared with Wilcoxon test to an anticipated lifetime risk of 20% (based on GÖTEBORG-1 trial). The secondary outcome was to determine factors associated with risk estimation in a multivariable linear regression model: previous prostate examination, family history, physical exercise, healthy diet, comorbidity, alcohol consumption, smoking, education level, marital status, urinary symptoms and erectile dysfunction.

resultsAmong PSA-tested men, the median estimated lifetime risk of prostate cancer was 30% (IQR 19% to 50%), corresponding to a 10 percentage-points higher estimation compared with the anticipated risk (p<0.001). Family history of prostate cancer, moderate to severe urinary symptoms and mild to moderate erectile dysfunction were associated with >5 percentage-points higher risk estimation. Similar results were obtained for non-PSA-tested men.

conclusionsMost men overestimated their prostate cancer risk which underscores the importance of providing them accurate information about prostate cancer. TRIAL REGISTRATION NUMBER: ISRCTN94604465.

Indexed as

Early Detection of CancerProstate-Specific AntigenProstatic NeoplasmsAgedHumansMaleMiddle AgedRisk AssessmentRisk FactorsSurveys and QuestionnairesSwedenProstate-Specific Antigenprostatesurveys and questionnairesurological tumours

Identifiers

PMID39153780
PMCPMC11331866

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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.