Evidence map›Paper›PMID 42375536›Full record

ArticleiScience2026

Dual modal pathomics model for colorectal cancer early recurrence prediction and mutation landscape analysis.

Wenyu Luo, Runze Liu, Xiaomei Yang, Wendan Si, Jinglei Qu, Ling Xu, Ying Chen, Na Song, Jin Wang, Yu Cheng and 3 more

Abstract read
In one paragraph

Article in iScience, 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.

Wenyu LuoDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, Liaoning, China.
Runze LiuZhejiang University and the University of Illinois Urbana-Champaign Institute, Zhejiang University, Haining 314400, Zhejiang, China.
Xiaomei YangDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, Liaoning, China.
Wendan SiDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, Liaoning, China.
Jinglei QuDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, Liaoning, China.
Ling XuDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, Liaoning, China.
Ying ChenDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, Liaoning, China.
Na SongDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, Liaoning, China.
Jin WangDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, Liaoning, China.
Yu ChengDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, Liaoning, China.
Xiujuan QuDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, Liaoning, China.
Xiaojiao GuanDepartment of Pathology, Shengjing Hospital of China Medical University, Shenyang 110001, Liaoning, China.
Ruichuan ShiDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with stage II/III colorectal cancer remain at substantial risk of early postoperative recurrence, yet accurate risk stratification remains challenging. Here, we developed a dual-modal pathomics model integrating hematoxylin-eosin and Ki-67 whole-slide images to predict early recurrence in 362 patients from two medical centers. Among multiple pretrained feature encoders, the integrated hematoxylin-eosin plus Ki-67 model using the UNI encoder achieved the best performance, with an area under the curve of 0.902 in the external validation cohort. The model consistently stratified patients into distinct prognostic groups across clinical subgroups. Attention map visualization further suggested that high-risk predictions were associated with tumor invasive fronts, whereas low-risk predictions were linked to immune infiltration and fibrotic stromal regions. These findings highlight the potential of multimodal pathology artificial intelligence for clinically interpretable prognostic assessment and personalized postoperative management in colorectal cancer.

Indexed as

health sciences

Identifiers

PMID42375536
PMCPMC13312108

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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.