Evidence map›Paper›PMID 36623239›Full record

ArticleJCO precision oncology2023

Internet-Based Germline Genetic Testing for Men With Metastatic Prostate Cancer.

Heather H Cheng, Alexandra O Sokolova, Roman Gulati, Deborah Bowen, Sarah A Knerr, Nola Klemfuss, Petros Grivas, Andrew Hsieh, John K Lee, Michael T Schweizer and 5 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in JCO precision oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
7.2field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 1 country.

Heather H ChengUniversity of Washington, Seattle, WA.ORCID 0000-0002-1365-0702
Alexandra O SokolovaOregon Health Science University, Portland, OR.
Roman GulatiFred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-7592-6567
Deborah BowenUniversity of Washington, Seattle, WA.
Sarah A KnerrUniversity of Washington, Seattle, WA.ORCID 0000-0001-5461-6298
Nola KlemfussUniversity of Washington, Seattle, WA.
Petros GrivasUniversity of Washington, Seattle, WA.ORCID 0000-0003-3965-3394
Andrew HsiehUniversity of Washington, Seattle, WA.ORCID 0000-0002-0897-1050
John K LeeUniversity of Washington, Seattle, WA.
Michael T SchweizerUniversity of Washington, Seattle, WA.ORCID 0000-0002-5510-0661
Todd YezefskiUniversity of Washington, Seattle, WA.ORCID 0000-0003-2518-1680
Alicia ZhouColor Health, Inc., Burlingame, CA.ORCID 0000-0003-0388-8909
Evan Y YuUniversity of Washington, Seattle, WA.ORCID 0000-0002-1510-8044
Peter S NelsonUniversity of Washington, Seattle, WA.ORCID 0000-0002-5451-5726
Bruce MontgomeryUniversity of Washington, Seattle, WA.ORCID 0000-0003-4459-0295
University of Washington · USFred Hutch Cancer Center · USOregon Health & Science University · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
TRAINING IN CANCER BIOLOGY &TRANSPLANTATIONT32CA009515 · NCI · UNIVERSITY OF WASHINGTON · PI NANCY ELLEN DAVIDSON, Effie W Petersdorf · 1985 to 2026
$16.2M
Statistical modeling to support population and translational cancer researchR50CA221836 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Roman Gulati · 2017 to 2026
$2.0M
NCATS NIH HHS UL1 TR002319NCI NIH HHS P30 CA015704NCI NIH HHS P50 CA097186NCI NIH HHS R50 CA221836NCI NIH HHS T32 CA009515
6 · The paper itself

Abstract

purposeGermline mutations in DNA repair genes are present in approximately 10% of men with metastatic prostate cancer (mPC), and guidelines recommend genetic germline testing. Notable barriers exist, including access to genetic counseling, insurance coverage, and out-of-pocket costs. The GENTleMEN study was designed to determine the feasibility of an Internet-based, patient-driven germline genetic testing approach for men with mPC. PATIENTS AND

methodsIn this prospective cohort study, men with mPC provided informed consent via an Internet-based platform and completed a questionnaire including demographics and family cancer history. Supporting medical data were also collected. Genetic testing was performed using the Color Genomics 30-gene targeted panel of cancer predisposition genes on a mailed saliva sample. Men whose test results identified a germline pathogenic or likely pathogenic variant received results by phone or telehealth genetic counseling; other participants received results by email with an option for phone-based or telehealth genetic counseling.

resultsAs of August 18, 2021, 816 eligible men were consented, of whom 68% (551) completed genetic testing, and 8.7% (48 of 551) were found to carry a pathogenic or likely pathogenic variant in a germline DNA repair gene:

conclusionHere, we show the feasibility of delivering germline (inherited) genetic testing by a voluntary, patient-driven, Internet-based platform to men with mPC. Preliminary results show rates of germline DNA repair mutations, consistent with other cohorts. Although feasible for some, reduced steps for participation, more dedicated diverse outreach and participant support, and identification and addressing of additional barriers is needed to ensure equitable access and optimization.

Indexed as

Genetic TestingProstatic NeoplasmsDNA RepairGerm CellsHumansMaleNeoplasm MetastasisProspective Studies

Identifiers

PMID36623239
PMCPMC9928882
OpenAlexW4313892761

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.