Evidence map›Paper›PMID 41862918›Full record

ArticleBMC medical informatics and decision making2026

AI-assisted tumor board decision-making in pancreatic oncology.

Markus Mergen, Felix Busch, Benjamin Schwarberg, Pia Koldeweihe, David Jungwirth, Jonas Sydlik, H Carlo Maurer, Marcus R Makowski, Daniel Spitzl, Florian T Gassert

Abstract read
In one paragraph

Article in BMC medical informatics and decision making, 2026. 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

10 authors.

Markus MergenDepartment of Diagnostic and Interventional Radiology, School of Medicine, TUM University Hospital, Technical University of Munich, Munich, Germany. markus.mergen@tum.de.
Felix BuschDepartment of Diagnostic and Interventional Radiology, School of Medicine, TUM University Hospital, Technical University of Munich, Munich, Germany.
Benjamin SchwarbergDepartment of Diagnostic and Interventional Radiology, School of Medicine, TUM University Hospital, Technical University of Munich, Munich, Germany.
Pia KoldeweiheDepartment of Diagnostic and Interventional Radiology, School of Medicine, TUM University Hospital, Technical University of Munich, Munich, Germany.
David JungwirthDepartment of Surgery, TUM University Hospital, TUM School of Medicine and Health, Technical University of Munich, Munich, Bavaria, Germany.
Jonas SydlikDepartment of Surgery, TUM University Hospital, TUM School of Medicine and Health, Technical University of Munich, Munich, Bavaria, Germany.
H Carlo MaurerMedical Clinic and Polyclinic II, TUM School of Medicine and Health, TUM University Hospital, Technical University Munich (TUM), Ismaningerstr. 22, 81675, Munich, Germany.
Marcus R MakowskiDepartment of Diagnostic and Interventional Radiology, School of Medicine, TUM University Hospital, Technical University of Munich, Munich, Germany.
Daniel Spitzl *Department of Diagnostic and Interventional Radiology, School of Medicine, TUM University Hospital, Technical University of Munich, Munich, Germany.
Florian T Gassert *Department of Diagnostic and Interventional Radiology, School of Medicine, TUM University Hospital, Technical University of Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic cancer requires nuanced, multidisciplinary treatment planning typically conducted within tumor boards. While Large Language Models (LLMs) have shown capabilities in medical reasoning, their ability to approximate complex, integrative decision-making in oncology remains underexplored.

methodsThis study evaluated the performance of LLaMA 3.3 (70b) in predicting tumor board decisions for newly diagnosed pancreatic cancer patients. Clinical documentation (including free-text imaging reports, pathology findings, and patient history) from 42 first-diagnosis cases discussed in a real-world tumor board was collected. The model was tasked with predicting one of three treatment options: surgical resection (SURG), neoadjuvant chemotherapy (NEO), or palliative therapy (PALL). Four prompting strategies were evaluated: zero-shot, advanced (adv.) zero-shot, Chain-of-Thought (CoT), and few-shot prompting. Performance was assessed using accuracy, micro- and macro-averaged F1 scores, and category-specific recall.

resultsThe advanced zero-shot and CoT strategies achieved the highest overall accuracy of 78.6% and a micro-averaged F1 score of 0.786. However, this performance was driven primarily by the correct classification of majority classes (SURG and PALL). Crucially, both high-accuracy strategies failed to identify any of the neoadjuvant therapy candidates (Recall NEO = 0.00; 0/7 cases), systematically misclassifying them as palliative or surgical. While few-shot prompting improved the detection of neoadjuvant cases (Recall NEO = 1.00), it introduced substantial noise, reducing overall accuracy to 56.7%. LLaMA 3.3 (70b) demonstrates high concordance with tumor board decisions for clear-cut surgical or palliative cases but exhibits a critical systematic failure in identifying candidates for neoadjuvant therapy. The high global accuracy masks a significant safety limitation regarding the recognition of complex, intermediate-stage patients.

conclusionThese findings suggest that current LLMs may approximate majority-class decisions but risk overlooking curative treatment pathways in nuanced scenarios, necessitating rigorous oversight and specific adaptation before clinical consideration.

Indexed as

Carcinoma, Pancreatic DuctalClinical Decision-MakingLarge Language ModelsMedical OncologyPancreatic NeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedNeoadjuvant TherapyPalliative CareRetrospective StudiesArtificial IntelligenceClinical Decision-MakingLarge Language ModelsPancreatic CancerTumor Board

Identifiers

PMID41862918
PMCPMC13064241

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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.