Evidence map›Paper›PMID 40410330›Full record

ArticleEuropean radiology2025

End-to-end prognostication in pancreatic cancer by multimodal deep learning: a retrospective, multicenter study.

Megan Schuurmans, Anindo Saha, Natália Alves, Pierpaolo Vendittelli, Derya Yakar, Sergio Sabroso-Lasa, Nannan Xue, Núria Malats, Henkjan Huisman, John Hermans and 1 more

Abstract readMulticenter Study
In one paragraph

Article in European radiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. From Routine Imaging to Risk Stratification: Multimodal Vision-Language Survival Modeling for Pancreatic Cancer.Proceedings. IEEE International Conference on Healthcare Informatics · 2026
    Article
  4. Article
  5. Review
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

11 authors.

Megan SchuurmansDiagnostic Image Analysis Group, Radboud University Medical Center, Nijmegen, The Netherlands. megan.schuurmans@radboudumc.nl.ORCID http://orcid.org/0000-0002-4939-6187
Anindo SahaDiagnostic Image Analysis Group, Radboud University Medical Center, Nijmegen, The Netherlands.
Natália AlvesDiagnostic Image Analysis Group, Radboud University Medical Center, Nijmegen, The Netherlands.
Pierpaolo VendittelliDiagnostic Image Analysis Group, Radboud University Medical Center, Nijmegen, The Netherlands.
Derya YakarDepartment of Medical Imaging, University Medical Center Groningen, Groningen, The Netherlands.
Sergio Sabroso-LasaGenetic and Molecular Epidemiology Group, Spanish National Cancer Research Center, Madrid, Spain.
Nannan XueGenetic and Molecular Epidemiology Group, Spanish National Cancer Research Center, Madrid, Spain.
Núria MalatsGenetic and Molecular Epidemiology Group, Spanish National Cancer Research Center, Madrid, Spain.
Henkjan HuismanDiagnostic Image Analysis Group, Radboud University Medical Center, Nijmegen, The Netherlands.
John HermansDepartment of Medical Imaging, Radboud University Medical Center, Nijmegen, The Netherlands.
Geert LitjensDiagnostic Image Analysis Group, Radboud University Medical Center, Nijmegen, The Netherlands.

Funding

Horizon 2020 101016851
6 · The paper itself

Abstract

objectivesPancreatic cancer treatment plans involving surgery and/or chemotherapy are highly dependent on disease stage. However, current staging systems are ineffective and poorly correlated with survival outcomes. We investigate how artificial intelligence (AI) can enhance prognostic accuracy in pancreatic cancer by integrating multiple data sources. MATERIALS AND

methodsPatients with histopathology and/or radiology/follow-up confirmed pancreatic ductal adenocarcinoma (PDAC) from a Dutch center (2004-2023) were included in the development cohort. Two additional PDAC cohorts from a Dutch and Spanish center were used for external validation. Prognostic models including clinical variables, contrast-enhanced CT images, and a combination of both were developed to predict high-risk short-term survival. All models were trained using five-fold cross-validation and assessed by the area under the time-dependent receiver operating characteristic curve (AUC).

resultsThe models were developed on 401 patients (203 females, 198 males, median survival (OS) = 347 days, IQR: 171-585), with 98 (24.4%) short-term survivors (OS < 230 days) and 303 (75.6%) long-term survivors. The external validation cohorts included 361 patients (165 females, 138 males, median OS = 404 days, IQR: 173-736), with 110 (30.5%) short-term survivors and 251 (69.5%) longer survivors. The best AUC for predicting short vs. long-term survival was achieved with the multi-modal model (AUC = 0.637 (95% CI: 0.500-0.774)) in the internal validation set. External validation showed AUCs of 0.571 (95% CI: 0.453-0.689) and 0.675 (95% CI: 0.593-0.757).

conclusionMultimodal AI can predict long vs. short-term survival in PDAC patients, showing potential as a prognostic tool in clinical decision-making. KEY POINTS: Question Prognostic tools for pancreatic ductal adenocarcinoma (PDAC) remain limited, with TNM staging offering suboptimal accuracy in predicting patient survival outcomes. Findings The multimodal AI model demonstrated improved prognostic performance over TNM and unimodal models for predicting short- and long-term survival in PDAC patients. Clinical relevance Multimodal AI provides enhanced prognostic accuracy compared to current staging systems, potentially improving clinical decision-making and personalized management strategies for PDAC patients.

Indexed as

Carcinoma, Pancreatic DuctalDeep LearningPancreatic NeoplasmsTomography, X-Ray ComputedAgedFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesArtificial intelligencePancreasPancreatic ductal carcinomaPrognosisRadiology

Identifiers

PMID40410330
PMCPMC12634761

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.