Evidence map›Paper›PMID 42404588›Full record

ArticleMedComm2026

Development and Validation of a Pathomics Model for Prognosis Prediction in Neoadjuvant Therapy-Treated Breast Cancer: A Retrospective, Multicenter Study.

Yani Wei, Wei Lou, Zongbo Han, Fan Yang, Fengling Li, Haofeng Li, Huijuan Shi, Bing Wei, Hongjun Li, Yuanyuan Zhao and 5 more

Abstract read
In one paragraph

Article in MedComm, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

15 authors.

Yani WeiDepartment of Pathology, West China Hospital Sichuan University Chengdu Sichuan China.
Wei LouCollege of Mathematical Medicine Zhejiang Normal University Jinhua Zhejiang China.
Zongbo HanState Key Laboratory of Networking and Switching Technology Beijing University of Posts and Telecommunications Beijing China.
Fan YangTencent AI Lab Shenzhen Guangdong China.
Fengling LiDepartment of Pathology, West China Hospital Sichuan University Chengdu Sichuan China.
Haofeng LiSchool of Systems Science and Engineering Sun Yat-sen University Guangzhou Guangdong China.
Huijuan ShiDepartment of Pathology, The First Affiliated Hospital Sun Yat-sen University Guangzhou Guangdong China.
Bing WeiDepartment of Pathology, West China Hospital Sichuan University Chengdu Sichuan China.
Hongjun LiDepartment of Pathology, The First Affiliated Hospital Sun Yat-sen University Guangzhou Guangdong China.
Yuanyuan ZhaoDepartment of Pathology, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University Taiyuan Shanxi China.
Xiuli XiaoDepartment of Pathology The Affiliated Hospital of Southwest Medical University Luzhou Sichuan China.
Yongquan YangInstitute of Clinical Pathology, West China Hospital Sichuan University Chengdu Sichuan China.
Anjia HanDepartment of Pathology, The First Affiliated Hospital Sun Yat-sen University Guangzhou Guangdong China.
Jianhua YaoTencent AI Lab Shenzhen Guangdong China.
Hong BuDepartment of Pathology, West China Hospital Sichuan University Chengdu Sichuan China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate outcome prediction is essential for personalized therapy in patients with breast cancer receiving neoadjuvant therapy (NAT). In this study, we developed and validated a multimodal artificial intelligence model, the ClinicHistomics Integrated Outcome Prediction Model (CIOPM), to predict prognosis in NAT-treated breast cancer patients by integrating clinicopathological data and hematoxylin and eosin (H&E)-stained surgical specimen whole-slide images (WSIs). A total of 847 WSIs from 835 patients across four multicenter cohorts collected between January 2008 and May 2020 were enrolled in model development and external validation. The CIOPM demonstrated robust predictive performance for overall survival (OS) and disease-free survival (DFS) in the two validation cohorts (VCs), yielding C-indices of 0.933 (95% CI: 0.878-0.977) and 0.915 (95% CI: 0.850-0.960) for OS in VC 1, and 0.947 (95% CI: 0.895-0.983) and 0.937 (95% CI: 0.905-0.965) for DFS in VC 2, respectively. The CIOPM enables accurate stratification of patients with NAT-treated breast cancer into high- and low-risk groups, achieving an AUC of 0.957 for both OS and DFS prediction. Moreover, it demonstrated superior performance in ablation studies, subgroup analyses, and clinical risk model comparisons. This model provides reliable risk stratification and personalized treatment decisions.

Indexed as

breast cancerdeep learningneoadjuvant therapyprognosiswhole‐slide image

Identifiers

PMID42404588
PMCPMC13329266

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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.