Evidence map›Paper›PMID 40020207›Full record

ArticleJCO precision oncology2025

Implementation of Cancer Genomics in the United States: Views of Payers and Other Stakeholders on Challenges and the Role of Payers in Solutions.

Julia R Trosman, Christine B Weldon, Allison W Kurian, Emily Mrig, Kathryn A Phillips

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. 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. Article
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

5 authors.

Julia R TrosmanUCSF Center for Translational and Policy Research on Precision Medicine (TRANSPERS), San Francisco, CA.ORCID 0000-0002-5583-2301
Christine B WeldonUCSF Center for Translational and Policy Research on Precision Medicine (TRANSPERS), San Francisco, CA.ORCID 0000-0003-3918-0048
Allison W KurianDepartments of Medicine and of Epidemiology and Population Health, Stanford University, Stanford, CA.ORCID 0000-0002-6175-9470
Emily MrigUCSF Center for Translational and Policy Research on Precision Medicine (TRANSPERS), San Francisco, CA.ORCID 0000-0003-4338-633X
Kathryn A PhillipsUCSF Center for Translational and Policy Research on Precision Medicine (TRANSPERS), San Francisco, CA.ORCID 0000-0003-0822-4968

Funding

BUILDING THE EVIDENCE BASE FOR APPROPRIATE AND EFFICIENT IMPLEMENTATION OF EMERGING GENOMIC TESTS FOR DISEASE MANAGEMENT AND SCREENINGR01HG011792 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PHILLIPS, KATHRYN A · 2021 to 2025
$4.6M
Promoting Access to Payment Pathways for Emerging Molecular DiagnosticsK01HG013687 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Emily A Hammad Mrig · 2024 to 2026
$618k
NHGRI NIH HHS K01 HG013687NHGRI NIH HHS R01 HG011792
6 · The paper itself

Abstract

purposeGenomic testing is crucial in cancer risk identification, diagnosis, and treatment. However, health care implementation is challenging, even for tests covered by insurance. US payers are important health care participants and may contribute to addressing implementation challenges. We explored whether and how payers consider their role in genomic test implementation, and the perspectives of nonpayer stakeholders on payers' participation.

methodsWe conducted a group interview with private payers (N = 12) to elucidate views on their role in genomic test implementation, implementation challenges, and potential solutions. Subsequently, we conducted individual interviews (N = 10) with nonpayer stakeholders-five cancer advocacy groups and five medical societies working in cancer, examining their reactions to payer input and capturing additional ideas. Qualitative research methods were used to frame the study and analyze results.

resultsPayers considered cancer genomics implementation important and expressed willingness and ability to be involved. They articulated specific challenges relevant to them, including underutilization of covered tests in clinical practice, inequitable test use, and inconsistencies across guidelines, and suggested specific solutions to collaborate on with other stakeholders. Stakeholders viewed payers' participation in implementation as appropriate and feasible, expressed willingness to work with payers where relevant, and concurred with the key challenges noted by payers. Stakeholders' agreement with payers' solutions varied, but they offered additional ideas for addressing challenges.

conclusionBoth payers and other stakeholders considered payers' role in addressing genomics implementation challenges appropriate and feasible, and offered specific avenues for payer participation. Our findings inform efforts by payers and other stakeholders to address broad health care implementation. They may also help precision oncology professionals, cancer centers, and health systems to frame their own implementation efforts and influence a broader policy and implementation agenda.

Indexed as

Genetic TestingGenomicsNeoplasmsHumansQualitative ResearchStakeholder ParticipationUnited States

Identifiers

PMID40020207
PMCPMC11875457

What OpenQuestion holds

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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.