Evidence map›Paper›PMID 37733980›Full record

Trial reportJCO oncology practice2023

Pretest Video Education Versus Genetic Counseling for Patients With Prostate Cancer: ProGen, A Multisite Randomized Controlled Trial.

Huma Q Rana, Jill E Stopfer, Michelle Weitz, Lindsay Kipnis, Diane R Koeller, Samantha Culver, Joanna Mercado, Rebecca Sue Gelman, Meghan Underhill-Blazey, Bradley A McGregor and 24 more

Open access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JCO oncology practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.9field-weighted citation impact, top 3% of its field
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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Mainstreaming genetic testing in community oncology settings.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Article
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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

34 authors at 5 institutions in 1 country.

Huma Q RanaMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-1598-6752
Jill E StopferMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-7724-3471
Michelle WeitzMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Lindsay KipnisCancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA.
Diane R KoellerCancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0003-1217-9514
Samantha CulverCancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA.
Joanna MercadoCancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA.
Rebecca Sue GelmanMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Meghan Underhill-BlazeyMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-1433-5915
Bradley A McGregorMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-8298-0289
Christopher J SweeneyMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-0398-6018
Nancie PetrucelliKarmanos Cancer Institute, Wayne State University, Detroit, MI.ORCID 0000-0003-2867-2119
Courtney KokenakesKarmanos Cancer Institute, Wayne State University, Detroit, MI.
Sara Pirzadeh-MillerUniversity of Texas Southwestern Medical Center, Dallas, TX.
Brian ReysUniversity of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0003-2430-8846
Arthur FrazierKarmanos Cancer Institute at McLaren Clarkston, Clarkston, MI.
Andrew KnechtlKarmanos Cancer Institute at McLaren Clarkston, Clarkston, MI.
Salman FatehKarmanos Cancer Institute at McLaren Clarkston, Clarkston, MI.
Donna Rachel VatnickCancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-3161-537X
Rebecca SilverLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0003-3730-2144
Kerry E KilbridgeMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Mark M PomerantzMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0003-4914-1157
Xiao X WeiMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Atish D ChoudhuryMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Guru P SonpavdeMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-1010-9611
Olga KozyrevaMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-7202-7972
Christopher LathanMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Carrie HortonAmbry Genetics, Aliso Viejo, CA.ORCID 0000-0001-5186-6208
Jill S DolinskyAmbry Genetics, Aliso Viejo, CA.ORCID 0000-0002-3854-9539
Elisabeth I HeathKarmanos Cancer Institute, Wayne State University, Detroit, MI.ORCID 0000-0003-1381-2713
Theodora Suzanne RossUniversity of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0002-9166-1802
Kevin Dale CourtneyUniversity of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0001-6273-3144
Judy E GarberMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-9449-3982
Mary-Ellen TaplinMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Dana-Farber Cancer Institute · USThe University of Texas Southwestern Medical Center · USThe Barbara Ann Karmanos Cancer Institute · USWayne State University · USAmbry Genetics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeGermline genetic testing (GT) is recommended for men with prostate cancer (PC), but testing through traditional models is limited. The ProGen study examined a novel model aimed at providing access to GT while promoting education and informed consent.

methodsMen with potentially lethal PC (metastatic, localized with a Gleason score of ≥8, persistent prostate-specific antigen after local therapy), diagnosis age ≤55 years, previous malignancy, and family history suggestive of a pathogenic variant (PV) and/or at oncologist's discretion were randomly assigned 3:1 to video education (VE) or in-person genetic counseling (GC). Participants had 67 genes analyzed (Ambry), with results disclosed via telephone by a genetic counselor. Outcomes included GT consent, GT completion, PV prevalence, and survey measures of satisfaction, psychological impact, genetics knowledge, and family communication. Two-sided Fisher's exact tests were used for between-arm comparisons.

resultsOver a 2-year period, 662 participants at three sites were randomly assigned and pretest VE (n = 498) or GC (n = 164) was completed by 604 participants (VE, 93.1%; GC, 88.8%), of whom 596 participants (VE, 98.9%; GC, 97.9%) consented to GT and 591 participants completed GT (VE, 99.3%; GC, 98.6%). These differences were not statistically significant although subtle differences in satisfaction and psychological impact were. Notably, 84 PVs were identified in 78 participants (13.2%), with

conclusionBoth VE and traditional GC yielded high GT uptake without significant differences in outcome measures of completion, GT uptake, genetics knowledge, and family communication. The increased demand for GT with limited genetics resources supports consideration of pretest VE for patients with PC.

Indexed as

Genetic CounselingProstatic NeoplasmsBRCA1 ProteinBRCA2 ProteinEstrogens, Conjugated (USP)HumansMaleMiddle AgedBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanEstrogens, Conjugated (USP)

Identifiers

PMID37733980
PMCPMC10667014
OpenAlexW4386916043

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.