Evidence map›Paper›PMID 40897976›Full record

ArticleDiscover oncology2025

Vision transformer network discovers the prognostic value of pancreatic cancer pathology sections via interpretable risk scores.

Zhiyong Peng, Yue Zhang, Tianchi Zhou, Wenjie Shi, Ya Wang, Maciej Pech, Georg Rose, Maximilian Dölling, Katrin Hippe, Roland S Croner and 2 more

Abstract read
In one paragraph

Article in Discover 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

12 authors.

Zhiyong PengSchool of Optoelectronic Engineering, Guilin University of Electronic Technology, Guilin, China.
Yue ZhangSchool of Optoelectronic Engineering, Guilin University of Electronic Technology, Guilin, China.
Tianchi ZhouMolecular and Experimental Surgery, Clinic for General-, Visceral-, Vascular- and Transplantation Surgery, Medical Faculty and University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany.
Wenjie ShiMolecular and Experimental Surgery, Clinic for General-, Visceral-, Vascular- and Transplantation Surgery, Medical Faculty and University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany.
Ya WangMolecular and Experimental Surgery, Clinic for General-, Visceral-, Vascular- and Transplantation Surgery, Medical Faculty and University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany.
Maciej PechClinic for Radiology and Nuclear Medicine, University Hospital Magdeburg, Magdeburg, Germany.
Georg RoseResearch Campus Stimulate, Otto von Guericke University, Magdeburg, Germany.
Maximilian DöllingMolecular and Experimental Surgery, Clinic for General-, Visceral-, Vascular- and Transplantation Surgery, Medical Faculty and University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany.
Katrin HippeInstitute of Pathology, Medical Faculty and University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany.
Roland S CronerMolecular and Experimental Surgery, Clinic for General-, Visceral-, Vascular- and Transplantation Surgery, Medical Faculty and University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany.
Yi ZhuDepartment of Gastroenterological Surgery, The Affiliated Hospital of Jiaxing University, Jiaxing, Zhejiang, China.
Ulf D KahlertMolecular and Experimental Surgery, Clinic for General-, Visceral-, Vascular- and Transplantation Surgery, Medical Faculty and University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany. ulf.kahlert@med.ovgu.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathological sections hold rich diagnostic information, yet their prognostic potential is underutilized. This study leverages deep learning to predict outcomes, advancing precision oncology of pathological sections with focus on pancreatic cancer. We analyzed H&E-stained whole section images of 125 cases from public databases as well as 28 real-world patients with pancreatic cancer and precancerous lesions. After image preprocessing, we identified and selected representative patches for subsequent analysis. We develop a modified visual transformer (ViT) model with spatial attention and fine-tuned on ImageNet2012, which was subsequently used to predict the survival times of the corresponding patients and to calculate risk scores. The modified ViT model demonstrated strong predictive accuracy for patient prognosis, with C-indices of 0.79 and 0.82 for Overall Survival (OS) and Disease Free Survival (DFS) in the test set and 0.62 in the validation set. Risk scores correlated well with patient survival, showing clustering between 0.17 and 0.95, aligning with a median survival of 24 months. Higher risk scores were associated with worse clinical prognosis, including shorter survival times and increased tumor recurrence risk, validated across all datasets. The model's AUCs for OS and DFS prediction reached 0.847/0.849 in the training set and 0.813/0.834 in the test set, confirming its high accuracy and potential for clinical application in risk stratification and prognosis prediction. ViT network can discover the prognostic value of pancreatic cancer pathology sections via interpretable risk scores, providing a new insight for prognosis evaluation as well as opens new technology building on existing clinical diagnostics.

Indexed as

Machine learningPancreatic cancerPersonalized medicineRisk scoreVision transformer

Identifiers

PMID40897976
PMCPMC12405124

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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.