Evidence map›Paper›PMID 40971753›Full record

ArticleJCO precision oncology2025

Patient-Reported Outcomes From Males Regarding Germline Testing for Prostate Cancer: Results From the PROGRESS Registry.

Stacy Loeb, Scott W Keith, Laura Gross, Rebecca L Hartman, Tomasz M Beer, Karina L Brierley, Heather H Cheng, Anna Couvillon, Adam P Dicker, Sue Friedman and 14 more

Abstract read
In one paragraph

Article in JCO precision oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

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

24 authors.

Stacy LoebDepartment of Urology and Population Health, New York University Langone Health and Manhattan Veterans Affairs, New York, NY.ORCID 0000-0003-3933-9207
Scott W KeithDivision of Biostatistics and Bioinformatics, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA.ORCID 0000-0002-9428-1151
Laura GrossSection of Medical Oncology, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.
Rebecca L HartmanDivision of Biostatistics and Bioinformatics, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA.ORCID 0009-0007-2952-3533
Tomasz M BeerOHSU Knight Cancer Institute, Oregon Health & Science University, Portland, OR.ORCID 0000-0001-5600-9993
Karina L BrierleySmilow Cancer Genetics and Prevention Program, Yale New Haven Hospital, New Haven, CT.ORCID 0009-0001-9545-8158
Heather H ChengDivision of Hematology and Oncology, Department of Medicine, University of Washington and Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-1365-0702
Anna CouvillonGenitourinary Malignancies Branch, National Cancer Institute, Bethesda, MD.
Adam P DickerSidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University, Philadelphia, PA.ORCID 0000-0003-0733-3337
Sue FriedmanFacing Our Risk of Cancer Empowered (FORCE), Tampa, FL.
Leonard G GomellaDepartment of Urology, Sidney Kimmel Comprehensive Cancer Center, Thomas Jefferson University, Philadelphia, PA.
Lawrence KarshAdventHealth Urology, Denver, CO.ORCID 0000-0002-3095-8303
William K KellyDepartment of Medical Oncology, Sidney Kimmel Comprehensive Cancer Center, Thomas Jefferson University, Philadelphia, PA.ORCID 0000-0003-2629-672X
Costas D LallasDepartment of Urology, Sidney Kimmel Comprehensive Cancer Center, Thomas Jefferson University, Philadelphia, PA.
Amy E LeaderSidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University, Philadelphia, PA.ORCID 0000-0002-9514-3631
Mark J MannDepartment of Urology, Sidney Kimmel Comprehensive Cancer Center, Thomas Jefferson University, Philadelphia, PA.
James Ryan MarkDepartment of Urology, Fox Chase Cancer Center, Philadelphia, PA.
Patrick MilleDepartment of Medical Oncology, Sidney Kimmel Comprehensive Cancer Center, Thomas Jefferson University, Philadelphia, PA.ORCID 0009-0002-6712-7180
Channing J PallerSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0003-3658-1858
Huma Q RanaDivision of Cancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-1598-6752
Alexandra O SokolovaHematology Oncology, Oregon Health and Science University, Portland, OR.ORCID 0000-0003-0821-6503
Edouard J TrabulsiDepartment of Urology, Jefferson Einstein Medical Center Philadelphia, Philadelphia, PA.ORCID 0000-0002-1058-6493
Young E WhangDivision of Oncology, Department of Medicine, University of North Carolina, Chapel Hill, NC.ORCID 0000-0002-1621-6661
Veda N GiriDepartment of Internal Medicine, Section of Medical Oncology, Yale Cancer Center and Yale School of Medicine, New Haven, CT.ORCID 0000-0002-7268-5913

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI Claudio Guillermo Giraudo · 1995 to 2026
$94.8M
TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
NCI NIH HHS P30 CA015704NCI NIH HHS P30 CA056036NCI NIH HHS P50 CA097186
6 · The paper itself

Abstract

purposeProstate cancer (PCA) germline testing (GT) informs precision therapy, cancer screening, and hereditary cancer risk for patients and families. To support patient-centered PCA GT, studying patient-reported outcomes (PROs) is essential.

methodsPROGRESS was a national patient-driven registry (January 2021-April 2022) for English-speaking males older than 18 years with previous/current PCA GT and Internet access. Surveys collected demographics, PCA history, family cancer history, mode of genetics care delivery, satisfaction with genetic counseling, decisional conflict, cancer genetics knowledge, and attitudes toward GT. Multiple linear regression modeling was used to estimate and draw inferences (α = .05) on strength of relationships between participant characteristics and PROs.

resultsAnalyses focused on 414 participants: White (88%), Black (3%), Asian (6%), and mixed/other (3%). Most participants were non-Hispanic (95.2%) and 46.9% had PCA. Genetic results were positive (pathogenic/likely pathogenic variants; mutations) in 27.9%. The three most common modes of genetics care were meeting with genetics professional (in-person or remotely; 30.9%), discussing with doctor (21.1%), and using website (20.8%). In covariate-adjusted models, satisfaction scores were highest with pretest counseling by phone (β = 1.31; 95% CI, 0.26 to 2.36) or discussion with doctor (β = 1.25; 95% CI, 0.38 to 2.12). Lower decisional conflict scores were reported for pretest counseling by phone (β = -3.76; 95% CI, -7.28 to -0.24). Males with mutations reported higher GT benefit scores (β = .30; 95% CI, 0.02 to 0.59) and importance of GT (β = .34; 95% CI, 0.08 to 0.61). Asian Americans reported lower GT satisfaction (β = -2.91; 95% CI, -4.34 to -1.48) and higher decisional conflict (β = 8.93; 95% CI, 4.36 to 13.51).

conclusionPROGRESS Registry informs the first comprehensive report of PROs among males undergoing PCA GT, providing insights into opportunities to improve patient experience and leverage the benefit of GT.

Indexed as

Genetic TestingPatient Reported Outcome MeasuresProstatic NeoplasmsAdultAgedGerm-Line MutationHumansMaleMiddle AgedRegistries

Identifiers

PMID40971753
PMCPMC12462908

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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.