Evidence map›Paper›PMID 42318461›Full record

ArticleFrontiers in oncology2026

Multimodal feature fusion model for breast mass malignant risk stratification.

Shengxin Pei, Xiumei Tang, Hongxia Su, Jingyan Liu, Zihan Lan, Siyu Wang, Yulan Peng

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Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Shengxin Pei *Department of Ultrasound, West China Hospital/West China School of Medicine, Sichuan University, Chengdu, China.
Xiumei Tang *Institute of Hospital Management, West China Hospital of Sichuan University, Chengdu, China.
Hongxia Su *West China School of Nursing, Sichuan University, Chengdu, China.
Jingyan LiuDepartment of Ultrasound, West China Hospital/West China School of Medicine, Sichuan University, Chengdu, China.
Zihan LanDepartment of Ultrasound, West China Hospital/West China School of Medicine, Sichuan University, Chengdu, China.
Siyu WangDepartment of Ultrasound, West China Hospital/West China School of Medicine, Sichuan University, Chengdu, China.
Yulan PengDepartment of Ultrasound, West China Hospital/West China School of Medicine, Sichuan University, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: This study aims to develop and validate machine learning models that integrate multimodal features (BI-RADS terminology, ultrasound imaging, and radiomics) to improve breast mass malignancy risk stratification and compare their diagnostic performance across different BI-RADS categories. Methods: This retrospective cohort study analyzed data from 2, 685 patients with 3, 703 ultrasound images collected from July 2019 to March 2024 at a single medical center. Patients included women with complete ultrasound images and clear pathological diagnoses. The dataset comprised 2, 069 benign cases (2, 762 images) and 616 malignant cases (941 images), randomly divided into training (n=2, 979 images) and validation (n=724 images) sets. Primary outcomes were diagnostic accuracy and area under the receiver operating characteristic curve (AUC) for distinguishing malignant from benign breast masses. Three machine learning models (Logistic Regression, Support Vector Machine, and Random Forest) were trained using BI-RADS terminology features, ultrasound quantitative features, radiomics features, and combined multimodal features. Performance was evaluated both overall and within specific BI-RADS subcategories (2, 3, 4a, 4b, 4c, and 5). Results: Among 2, 685 patients, the Random Forest model using combined multimodal features achieved the highest overall performance with an AUC of 0.850 (95% CI 0.810- 0.875). For single-modality approaches, Logistic Regression performed best with BI-RADS terminology features, with an AUC of 0.820 (95% CI, 0.775-0.856), and radiomics features, with an AUC of 0.740 (95% CI, 0.706-0.780); while Random Forest was optimal for ultrasound imaging features, with an AUC of 0.800 (95% CI, 0.768-0.839). Subgroup analysis revealed excellent performance for BI-RADS categories 2 (AUC, 1.000-1.000) and 3 (AUC, 0.947-0.957), acceptable performance for 5 (AUC, 0.813-0.870) and 4a (AUC, 0.800-0.867), but poor performance for categories 4b (AUC, 0.649-0.709), 4c (AUC, 0.551-0.623). Discussion: This study demonstrates that machine learning models integrating multimodal ultrasound features can effectively stratify breast mass malignancy risk, with the Random Forest model using combined features showing superior performance. The approach shows particular strength in BI-RADS categories 2, 3, 5 and 4a, suggesting potential clinical utility for reducing unnecessary biopsies and improving diagnostic confidence. However, performance limitations in higher-risk categories (4b, 4c) indicate need for further model refinement and multicenter validation before clinical implementation.

Indexed as

artificial intelligencebreast cancermachine learningmultimodal datarisk stratification

Identifiers

PMID42318461
PMCPMC13272049

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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.