Pulse Brain · Growing Health Evidence Index
Tier 2 — RCT / large cohortPeer-reviewed

Effect of a Low-Intensity PSA-Based Screening Intervention on Prostate Cancer Mortality

Richard M. Martin, Jenny Donovan, Emma L. Turner, Chris Metcalfe, Grace Young, Eleanor Walsh, J. Athene Lane, Sian Noble, Steven Oliver, Simon Evans, Jonathan A C Sterne, Peter Holding, Yoav Ben‐Shlomo, Peter Brindle, Naomi Williams, Elizabeth Hill, Siaw Yein Ng, Jessica Toole, Marta Tazewell, Laura J. Hughes, Charlotte Davies, Joanna Thorn, Liz Down, George Davey Smith, David E. Neal, Freddie C. Hamdy, CAP Trial Group

JAMA · 2018

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Summary

The CAP trial, a large UK-based cluster randomized controlled trial of 415,357 men aged 50–69, found that a single PSA screening intervention with standardized diagnostic pathway resulted in no significant difference in prostate cancer-specific mortality compared to standard practice at 10-year follow-up (rate ratio 0.96; 95% CI 0.85–1.08). Although 40% of the intervention group attended screening and 36% underwent PSA testing, with 85% of those with elevated PSA undergoing biopsy, these efforts did not translate into a measurable mortality benefit, informing the ongoing debate about the net benefits and harms of prostate cancer screening.

UK applicability

As a primary UK study conducted across 573 NHS general practices, the findings directly inform UK screening policy and clinical practice. The results suggest that single-occasion PSA screening with systematic follow-up in primary care does not confer prostate cancer mortality reduction in this population, relevant to UK National Screening Committee guidance on prostate cancer screening.

Key measures

Prostate cancer-specific mortality (per 1000 person-years); rate ratio and rate difference at 10-year follow-up; PSA attendance and testing uptake; biopsy rates among those with PSA 3–19.9 ng/mL; diagnostic stage and Gleason grade distribution

Outcomes reported

The study measured prostate cancer-specific mortality at a median 10-year follow-up in men aged 50–69 years invited to PSA screening versus standard practice. Secondary outcomes included diagnostic cancer stage, Gleason grade, all-cause mortality, and causal effects of attending screening.

Theme
Measurement & metrics
Subject
Measurement methods & nutrient profiling
Study type
Research
Study design
Cluster randomized controlled trial
Source type
Peer-reviewed study
Status
Published
Geography
United Kingdom
System type
Human clinical
DOI
10.1001/jama.2018.0154
Catalogue ID
BFmor3gaas-g389ri

Topic tags

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