Evidence map›Paper›PMID 42372208›Full record

ArticleJCO precision oncology2026

Implementing Timely Germline Genetic Testing for Patients With Pancreatic Cancer Using a Genetics Copilot for Point-of-Care Education and Health Assessment.

Sophie Moravec, Laura V Barton, Revathy Suresh, Laura Hayward, Tara Schmidlen, Jessica N Rivera Rivera, Toni Basinski, Solomon Alhassan, Nicole Nardella, Adrianna Oraiqat and 19 more

Abstract read
In one paragraph

Article in JCO precision oncology, 2026. 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

29 authors.

Sophie MoravecDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.
Laura V BartonDepartment of Pathology, Moffitt Cancer Center, Tampa, FL.
Revathy SureshDepartment of Pathology, Moffitt Cancer Center, Tampa, FL.
Laura HaywardNest Genomics, New York, NY.
Tara SchmidlenNest Genomics, New York, NY.
Jessica N Rivera RiveraHealthcare Delivery Research Network, MedStar Health Research Institute, Washington, DC.ORCID 0000-0002-6675-0037
Toni BasinskiDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.ORCID 0009-0002-9537-578X
Solomon AlhassanDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.
Nicole NardellaDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.ORCID 0009-0001-7392-6336
Adrianna OraiqatDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.
Leticia CraigDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.
Laura CooperDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.
Carmelo J BlanquicettDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0003-1041-2490
Satish S MaharajDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0002-2872-3011
Kirsten BlueDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.
Melissa AdamsDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.
Richard KimDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0002-8448-844X
Tiago Biachi De CastriaDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0001-6832-2485
Mokenge MalafaDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.
Andrew J SinnamonDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0001-6031-6451
Allan Lima PereiraDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0002-8573-7364
Dae Won KimDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.
Sarah HoffeDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.
Pamela J HodulDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.
Susan T VadaparampilDepartment of Health Outcomes and Behavior, Moffitt Cancer Center, Tampa, FL.
Teresa T HoDepartment of Pathology, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0002-2489-3099
J Kevin HicksDepartment of Pathology, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0003-2314-0164
Moran SnirNest Genomics, New York, NY.
Jennifer B PermuthDepartment of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0002-4726-9264

Funding

Using Radiogenomics to Noninvasively Predict the Malignant Potential of Intraductal Papillary Mucinous Neoplasms of the Pancreas and Uncover Hidden BiologyR37CA229810 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI JEONG, DANIEL, PERMUTH, JENNIFER B · 2019 to 2025
$5.0M
NCI NIH HHS R37 CA229810
6 · The paper itself

Abstract

purposePancreatic ductal adenocarcinoma (PDAC) ranks third in cancer-related deaths. Although national guidelines recommend germline multigene panel testing (MGPT) for all patients with PDAC, only 6%-19% undergo testing, mostly due to under-referral and genetic counselor shortages. We evaluated a coordinator-led and digitally supported workflow designed to increase access to pretest education, improve MGPT uptake, and reduce turnaround time (TAT) for patients newly diagnosed with PDAC at our center.

methodsThrough the Genetic Information for Treatment Decisions (GIFTD) Initiative, a Genetic Risk Education Coordinator (GREC) served as a liaison between providers, genetic counselors, and patients. Subsequently, we partnered with Nest Genomics to develop the GIFTD Partially Automated Nest Copilot (G-PANC), a digital tool that collects cancer history, delivers genetic education, and assesses MGPT interest before coordinator follow-up. Outcomes included genetic education completion, MGPT uptake, and TAT across sequential phases (baseline, GREC-only, and G-PANC [GREC+ Nest Copilot]).

resultsOver 1 year, 354 patients with PDAC were invited to access G-PANC; 73% activated accounts, 80% completed education, and 63% expressed MGPT interest. Among those completing education, 86% engaged with the GREC, and 81% consented to testing, including 15 initially uninterested patients. Of the 127 patients tested, 13% had pathogenic variants. Compared with a baseline/traditional workflow, the GREC-only phase was associated with increased MGPT uptake (43% to 80%) and reduced TAT (54 to 30 days). During the subsequent G-PANC phase, testing uptake remained high (77%) and TAT further decreased to 22 days.

conclusionA coordinator-led workflow substantially increased MGPT uptake and reduced TAT. Digital education integration was feasible, maintained high testing rates, and reduced TAT. Prospective evaluation will clarify the independent contributions of digital automation.

Indexed as

Carcinoma, Pancreatic DuctalGenetic TestingPancreatic NeoplasmsPoint-of-Care TestingAgedFemaleGerm-Line MutationHumansMaleMiddle Aged

Identifiers

PMID42372208
PMCPMC13366501

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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.