Evidence map›Paper›PMID 42661205›Full record

Trial reportBMC medical genomics2026

Development and pilot testing of a prostate cancer polygenic risk report.

Julia N Griffin, Morgan E Danowski, Haley L Gerety, Katherine Lafferty, Marla L Clayman, Ashley A Antwi, Mercedes G Bertero, Charles A Brunette, Chris Gillespie, Louise Guentert and 4 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC medical genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05926102 (The Prostate Cancer, Genetic Risk, and Equitable Screening Study), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

NCT05926102 narecruitingnot on this map

The Prostate Cancer, Genetic Risk, and Equitable Screening Study (ProGRESS): A Pragmatic Trial of Precision Prostate Cancer Screening

TypeinterventionalSponsorVA Office of Research and DevelopmentRan2024 to 2030Enrolled5,000ConditionsProstate CancerArmsPrecision screening intervention, Usual care
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Julia N GriffinBoston University Genetic Counseling Program, Boston, MA, USA.
Morgan E DanowskiVA Boston Healthcare System, Boston, MA, USA.
Haley L GeretyVA Boston Healthcare System, Boston, MA, USA.
Katherine LaffertyBroad Clinical Labs, Broad Institute of MIT and Harvard, Burlington, MA, USA.
Marla L ClaymanCenter for Health Optimization and Implementation Research (CHOIR), VA Bedford Healthcare System, Bedford, MA, USA.
Ashley A AntwiVA Boston Healthcare System, Boston, MA, USA.
Mercedes G BerteroCenter for Health Optimization and Implementation Research (CHOIR), VA Bedford Healthcare System, Bedford, MA, USA.
Charles A BrunetteVA Boston Healthcare System, Boston, MA, USA.
Chris GillespieCenter for Health Optimization and Implementation Research (CHOIR), VA Bedford Healthcare System, Bedford, MA, USA.
Louise GuentertVA Boston Healthcare System, Boston, MA, USA.
Niall J LennonBroad Clinical Labs, Broad Institute of MIT and Harvard, Burlington, MA, USA.
Julian MartinVA Boston Healthcare System, Boston, MA, USA.
Lauren S PatelVA Boston Healthcare System, Boston, MA, USA.
Jason L VassyVA Boston Healthcare System, Boston, MA, USA. jvassy@bwh.harvard.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPolygenic risk scores (PRS) are increasingly being incorporated into clinical care, yet optimal strategies for communicating PRS results to patients and clinicians remain undefined. Effective report design is critical to ensure comprehension and appropriate use, particularly for complex conditions such as prostate cancer where screening decisions are nuanced. We developed and pilot tested patient-facing materials to communicate integrated polygenic and monogenic risk for prostate cancer in the context of a randomized clinical trial.

methodsWe designed a summary report and accompanying Frequently Asked Questions (FAQ) page to communicate prostate cancer genetic risk within the Prostate Cancer, Genetic Risk, and Equitable Screening Study (ProGRESS). Materials were developed through an iterative, multidisciplinary process informed by existing literature on genomic risk communication. We conducted semi-structured interviews with a national sample of eight men eligible for prostate cancer screening to evaluate comprehension, interpretation of visual elements, perceived usefulness, and preferences for improvement. Interviews were transcribed and analyzed using reflexive thematic analysis.

resultsParticipants generally found the summary report and FAQ page understandable and visually engaging. Graphical displays of absolute risk, particularly pictograph arrays, facilitated comprehension and helped contextualize risk. Visual cues such as color and bold formatting effectively directed attention to key information, with red coloring perceived as particularly salient for high-risk results. In contrast, more complex visualizations, including bell curves and incidence curves, were frequently misunderstood or not interpreted as intended. Participants expressed a desire for clearer guidance regarding next steps and additional accessible information, suggesting supplementary resources such as hyperlinks or QR codes. Concerns about readability included small font size and high text density.

conclusionsIn this qualitative pilot study, patient-facing materials for communicating prostate cancer PRS were generally well received, with specific design features such as simple visualizations and clear formatting enhancing understanding. Findings highlight the importance of intuitive risk displays and actionable guidance in PRS reporting. These results provide practical insights to inform the design of genomic risk reports as PRS-based prostate cancer screening approaches move toward clinical implementation.

trial registrationClinicalTrials.gov NCT05926102; date of registry: July 3, 2023.

Indexed as

Genetic Risk ScoreProstatic NeoplasmsAgedHumansMaleMiddle AgedPilot ProjectsGenomicsPolygenic risk scores (PRS)Prostate cancer screeningQualitative researchRisk communication

Identifiers

PMID42661205
PMCPMC13520487

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Registered trials

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.