Evidence map›Paper›PMID 41507565›Full record

ArticleBritish journal of cancer2026

Prognostic model for pancreatic cancer based on machine learning of routine slides and transcriptomic tumor analysis.

Manabu Takamatsu, Mariko Tanaka, Yohei Masugi, Yosuke Inoue, Hiroko Nagano, Tho Ngoc-Quynh Le, Kenji Nishida, Yui Sawa, Kota Sugiura, Yoshikuni Kawaguchi and 18 more

Abstract read
In one paragraph

Article in British journal of cancer, 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

28 authors.

Manabu Takamatsu *Division of Pathology, Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan. manabu.takamatsu@jfcr.or.jp.ORCID http://orcid.org/0000-0001-9601-5802
Mariko Tanaka *Department of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Yohei Masugi *Department of Pathology, Keio University School of Medicine, Tokyo, Japan.
Yosuke InoueDivision of Hepatobiliary and Pancreatic Surgery, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Hiroko NaganoDivision of Pathology, Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.
Tho Ngoc-Quynh LeDepartment of Pathology, University Medical Center Ho Chi Minh City, Ho Chi Minh City, Vietnam.
Kenji NishidaDivision of Pathology, Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.
Yui SawaDivision of Hepatobiliary and Pancreatic Surgery, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Kota SugiuraDivision of Hepatobiliary and Pancreatic Surgery, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Yoshikuni KawaguchiHepato-Biliary-Pancreatic Surgery Division, Department of Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0003-2986-3224
Yusuke KazamiHepato-Biliary-Pancreatic Surgery Division, Department of Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Yousuke NakaiDepartment of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Tsuyoshi HamadaDepartment of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan. hamada-tky@umin.ac.jp.ORCID http://orcid.org/0000-0002-3937-2755
Tatsunori SuzukiDepartment of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Kensuke HaraDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan.
Yutaka KurebayashiDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan.ORCID http://orcid.org/0000-0003-3773-0851
Tsuyoshi TakedaDepartment of Hepato-Biliary-Pancreatic Medicine, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Naoki SasahiraDepartment of Hepato-Biliary-Pancreatic Medicine, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Yosuke UematsuDepartment of Surgery, Keio University School of Medicine, Tokyo, Japan.
Sho UemuraDepartment of Surgery, Keio University School of Medicine, Tokyo, Japan.
Mitsuhiro FujishiroDepartment of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0002-4074-1140
Kiyoshi HasegawaHepato-Biliary-Pancreatic Surgery Division, Department of Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Minoru KitagoDepartment of Surgery, Keio University School of Medicine, Tokyo, Japan.
Yu TakahashiDivision of Hepatobiliary and Pancreatic Surgery, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID http://orcid.org/0000-0003-3066-023X
Shigeki SekineDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan.
Tetsuo UshikuDepartment of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0002-1763-8380
Kengo TakeuchiDivision of Pathology, Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID http://orcid.org/0000-0002-1599-5800
GTK Pancreatic Cancer Study Group in Japan

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) JP19K08362MEXT | Japan Society for the Promotion of Science (JSPS) JP20K07414MEXT | Japan Society for the Promotion of Science (JSPS) JP21K15368MEXT | Japan Society for the Promotion of Science (JSPS) JP21K15393MEXT | Japan Society for the Promotion of Science (JSPS) JP22H02841MEXT | Japan Society for the Promotion of Science (JSPS) JP23K15485
6 · The paper itself

Abstract

backgroundPrognostication for pancreatic ductal adenocarcinoma (PDAC) using histologic images is difficult due to tumor heterogeneity. We developed an artificial intelligence (AI) model to predict postoperative recurrence using histologic image patches.

methodsWe included 591 patients with resected PDAC to train an AI model for recurrence prediction at 12 or 24 months and validated it using external cohorts (n = 302 in total). Image patches from hematoxylin and eosin-stained slides were clustered via uniform manifold approximation and projection (UMAP) and used to train a random forest model. Predictive performance was evaluated using area under the receiver operating characteristic curve (AUC). Gene expression analysis was conducted to characterise survival-related clusters.

resultsSeventeen patch clusters were identified. Two were linked to high recurrence risk, and one to low risk. In external validation, the model achieved an AUC of up to 0.792. The random forest score independently predicted recurrence. Greater heterogeneity in patch composition correlated with shorter time to recurrence (P < 0.01). High-risk clusters showed elevated CSF3R expression; the low-risk cluster showed increased IGFBP3 expression.

conclusionsOur AI model, using only archival histologic slides, accurately predicted postoperative recurrence in PDAC and revealed image features linked to outcomes and gene expression.

Indexed as

Carcinoma, Pancreatic DuctalMachine LearningNeoplasm Recurrence, LocalPancreatic NeoplasmsAgedFemaleGene Expression ProfilingHumansInsulin-Like Growth Factor Binding Protein 3MalePrediction AlgorithmsPredictive Learning ModelsPrognosisRandom ForestTranscriptomeIGFBP3 protein, humanInsulin-Like Growth Factor Binding Protein 3

Identifiers

PMID41507565
PMCPMC12960721

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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.