Evidence map›Paper›PMID 42244816›Full record

ArticleArXiv2026

Digitally enriching a screening population for pancreatic cancer using routine blood-based measures and clinical histories.

Chris Varghese, Leo Y Li-Han, Richa Bisht, Ellen Larson, Frank Lee, Ryan M Carr, Tanios S Bekaii-Saab, Shounak Majumder, John D Halamka, Mark Truty and 3 more

Abstract readPreprint
In one paragraph

Article in ArXiv, 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

13 authors.

Chris VargheseDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
Leo Y Li-HanDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
Richa BishtDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
Ellen LarsonDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
Frank LeeDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
Ryan M CarrDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
Tanios S Bekaii-SaabDepartment of Hematology and Oncology, Mayo Clinic, Phoenix, AZ, USA.
Shounak MajumderDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
John D HalamkaMayo Clinic Platform, Mayo Clinic, Rochester, Minnesota.
Mark TrutyDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
Ajit H GoenkaDepartment of Radiology, Mayo Clinic, Rochester, Minnesota.
Hojjat SalehinejadDivision of Health Care Delivery Research, Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, MN, USA.
Cornelius A ThielsDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.

Funding

Optimizing Pancreatic Cancer Management with Next Generation Imaging and Liquid BiopsyR01CA256969 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Eric Collisson, Ajit Harishkumar Goenka · 2021 to 2026
$3.1M
Quantitative In Vivo 68Ga-Fibroblast-Activation-Protein-Inhibitors (FAPI)-46 PET Imaging of Cancer-Associated Fibroblasts (CAFs) in Pancreatic Ductal Adenocarcinoma (PDA)R01CA272628 · NCI · MAYO CLINIC ROCHESTER · PI GOENKA, AJIT HARISHKUMAR · 2022 to 2025
$2.5M
NCI NIH HHS R01 CA256969NCI NIH HHS R01 CA272628
6 · The paper itself

Abstract

Earlier detection of pancreatic cancer is key to enabling wider access to curative treatment and reducing cancer deaths; however, screening is presently not viable. Latent indicators of pathology are evident in an individual's disease and blood test trajectories and may predict the development of pancreatic cancer. Longitudinal sequences of coded diagnoses and blood test values accrued by patients throughout their clinical interactions were used to train a custom Transformer-based neural network with a multi-head attention mechanism to predict risk of pancreatic cancer with a multi-year lead time and risk-stratify populations for targeted screening. The cohort comprised 6,017 adults with pancreatic cancer and 177,081 controls (overall median age 75, 45% female) with median 12 years (interquartile range 6.9-16.2) of medical history prior to pancreatic cancer diagnosis. External validation via leave-one-site-out, out-of-sample testing predicting pancreatic cancer 1-, 2-, and 3-years prior to diagnosis demonstrated mean area under the receiver operating characteristic of 0.837 (95% confidence interval 0.827-0.848), 0.797 (95% confidence interval 0.782-0.813), and 0.760 (95% confidence interval 0.745-0.776), respectively. Estimated pancreatic cancer risks were well-calibrated (calibration plot slope 1.08, intercept of -0.077; Brier score 0.025), and a Bayesian population pancreatic cancer prevalence update allows estimated cancer risk outputs to be transportable across settings. At testing, a screening threshold of >3.3% risk of pancreatic cancer in 1-year offered a diagnostic odds ratio of 18.2. Our work therefore lays the foundation for a first population-level digital enrichment tool to widen access to curative-intent management of pancreatic cancer.

Indexed as

cancer screeningearly detectionpancreatic cancerpredictiontransformer model

Identifiers

PMID42244816
PMCPMC13232437

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.