Evidence map›Paper›PMID 42015666›Full record

Trial reportInternational journal of cancer2026

Evaluating the Impact of Age on Prostate Cancer Overdiagnosis Using Long-Term Follow-Up From the CAP Randomised Trial.

Adam R Brentnall, Matejka Rebolj, Peter Sasieni, Garth Funston, Rhian Gabe, Andrew J Vickers

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in International journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Adam R BrentnallWolfson Institute of Population Health, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0001-6327-4357
Matejka ReboljWolfson Institute of Population Health, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0001-9597-645X
Peter SasieniWolfson Institute of Population Health, Queen Mary University of London, London, UK.
Garth FunstonWolfson Institute of Population Health, Queen Mary University of London, London, UK.
Rhian GabeWolfson Institute of Population Health, Queen Mary University of London, London, UK.
Andrew J VickersMemorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID https://orcid.org/0000-0003-1525-6503

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Cancer Research UK C8162/A29083NCI NIH HHS P30 CA008748NIH HHS P30 CA008748NIH HHS P50-CA92629
6 · The paper itself

Abstract

Prostate cancer overdiagnosis is detection of prostate cancer through PSA testing that otherwise would not have been diagnosed within the patient's lifetime. It is a major concern to policymakers due to its impact on quality of life. We used long-term follow-up data from the CAP randomised trial of a one-off screen, and English male competing mortality rates (2021-23), to estimate the impact of age on excess prostate cancer incidence within 15 years ('overdiagnosis') using competing-risks methods. In total, 2249 (1.19%) of 189,386 men invited for a PSA test in CAP had cancer detected at the one-off screen. Prostate cancer cumulative incidence at 15 years was 7.08% (95% CI 6.95%-7.21%) in those invited to screening, compared with 6.94% (95% CI 6.82%-7.06%) in the control arm; an absolute excess incidence difference of 0.14% (95% CI -0.04% to 0.37%). Excess net incidence to 15 years was 0.14/1.19 = 11.7% (95% CI 0.0%-26.7%) of cases detected at a single prevalent screen. Accounting for competing mortality, men diagnosed at screening aged 50 years were projected to have a 16% chance the cancer would not have been detected within 15 years, rising to 32% if detected at screening aged 70 years and 58% aged 80 years. Thus, prostate cancer overdiagnosis rises substantially with age due to competing mortality, and is relatively low for younger men. Accordingly, policies that enable opportunistic testing should be re-examined in settings where they have led to high rates of screening in older men.

Indexed as

OverdiagnosisProstatic NeoplasmsAgedAge FactorsEarly Detection of CancerFollow-Up StudiesHumansIncidenceMaleMass ScreeningMiddle AgedProstate-Specific AntigenProstate-Specific Antigenoverdiagnosisprostate cancerPSA testingscreening

Identifiers

PMID42015666
PMCPMC13340977

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Registered trials

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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.