Evidence map›Paper›PMID 40366732›Full record

ArticleJMIR formative research2025

Developing the MyCancerGene Digital Health Portal to Improve Patients' Understanding of Germline Cancer Genetic Test Results: Development, User, and Usability Testing Study.

Phillip Trieu, Dominique Fetzer, Briana McLeod, Kathryn Schweickert, Lauren Gutstein, Brian Egleston, Susan Domchek, Linda Fleisher, Lynne Wagner, Kuang-Yi Wen and 9 more

Abstract read
In one paragraph

Article in JMIR formative research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Trial
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

19 authors.

Phillip TrieuDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0009-0006-2973-4288
Dominique FetzerDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0000-0001-6374-0151
Briana McLeodDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0000-0001-9103-9397
Kathryn SchweickertDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0009-0009-4571-1256
Lauren GutsteinDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0009-0008-3266-9979
Brian EglestonFox Chase Cancer Center, Temple University, Philadelphia, PA, United States.ORCID 0000-0002-1633-799X
Susan DomchekDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0000-0002-5914-7272
Linda FleisherFox Chase Cancer Center, Temple University, Philadelphia, PA, United States.ORCID 0000-0002-6911-0756
Lynne WagnerGrillings School of Global Public Health, University of North Carolina, Chapel Hill, NC, United States.ORCID 0000-0001-9685-4796
Kuang-Yi WenThomas Jefferson University, Philadelphia, PA, United States.ORCID 0000-0002-4133-1178
Cara CacioppoDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0000-0003-4761-7027
Jessica E EbrahimzadehDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0000-0002-1505-9625
Dana FalconeDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0009-0001-0112-2603
Claire LangerDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0009-0000-4064-2989
Elisabeth WoodDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0000-0002-4734-2214
Kelsey KarpinkDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0009-0005-2636-0973
Shelby PosenDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0009-0002-2433-3689
Enida SelmaniDivision of Hematology-Oncology, Abramson Cancer Center, The University of Pennsylvania, Philadelphia, PA, United States.ORCID 0009-0002-6784-7874
Angela R BradburyUniversity of Pennsylvania, Philadelphia, PA, United States.ORCID 0000-0001-9607-6402

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Eric Andrew Ross · 1985 to 2026
$138.8M
NCI NIH HHS P30 CA006927
6 · The paper itself

Abstract

backgroundThe use of multigene panels has significantly increased the likelihood that genetic testing will leave patients with uncertainties regarding test interpretation, implications, and recommendations, which will change over time. Effective longitudinal care models are needed to provide patients with updated information and to obtain patient and family history updates.

objectiveTo bridge this gap, we aimed to develop a patient- and genetic provider-informed digital genetic health portal (GHP), MyCancerGene, to improve longitudinal patient understanding of and responses to genetic testing.

methodsWe used a 5-step process to develop MyCancerGene. To better understand their interest in and willingness to use a digital GHP, we surveyed 307 patients who completed genetic testing (step 1). We completed qualitative interviews with 10 patients and a focus group with 17 genetic providers to inform the content and function of MyCancerGene (step 2). Next, we developed initial intervention content (step 3) and completed user testing of intervention content with 25 providers and 28 patients (step 4). After developing the prototype intervention, we completed usability testing with 8 patients for their feedback on the final content, functions, and ease of use (step 5).

resultsIn surveys conducted in step 1, 90% of patients with positive results reported interest in a digital GHP, and over 75% of participants with variants of uncertain significance or uninformative negative results reported similar interest. The most frequently reported advantages among patients were increasing accessibility, convenience, and efficiency (103/224, 46%); keeping genetic information organized (54/224, 24.1%); and increasing or maintaining patient understanding of the information (38/224, 17%). In qualitative interviews (step 2), both patients and genetic providers endorsed the benefit of the tool for updating personal and family history and for providers to share new risk information, test interpretation, or other medical changes. Patient and provider input informed eight key components of the tool: (1) Landing Page, (2) Summary of Care page, (3) My Genetic Test Results page, (4) My Family History page, (5) Provide an Update page, (6) Review an Update page, (7) Resources page, and (8) the Screenings Tracker. They also recommended key functions, including the ability to download and print materials and the inclusion of reminders and engagement functions. Potential challenges identified by patients included privacy and security concerns (67/206, 32.5%) and the potential for electronic information to generate distress (20/206, 9.7%). While patients were comfortable with updates (ie, even variant reclassification upgrades or clinically significant results), 44% (11/25) of genetic providers were uncomfortable sharing variant reclassification upgrades through MyCancerGene.

conclusionsMyCancerGene, a patient-centered digital GHP, was developed with extensive patient and genetic provider feedback and designed to enhance longitudinal patient understanding of and affective and behavioral responses to genetic testing, particularly in the era of evolving evidence and risk information.

Indexed as

Genetic TestingNeoplasmsPatient PortalsAdultAgedComprehensionDigital HealthFemaleFocus GroupsHumansMaleMiddle AgedQualitative ResearchSurveys and Questionnairesclinical practicedigital healthdigital intervention developmentdigital tooleffectivenesselectronic informationgenetic health portalgenetic medicinegermline cancerhealth portalinterventionlikelihoodlongitudinal caremedical historymultigene panelspatient-centered contentrisk informationusability

Identifiers

PMID40366732
PMCPMC12120370

What OpenQuestion holds

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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.