Evidence map›Paper›PMID 42690533›Full record

ArticleVisual computing for industry, biomedicine, and art2026

Lightweight Transformer-based knowledge distillation framework for high-dimensional spatiotemporal radiomics in breast cancer risk prediction.

Haofan Huang, Han Zhou, Kaibin Huang, Jie Yang, Peixi Ying, Puxiang Lai, Yan Lin, Yi Gao

Abstract read
In one paragraph

Article in Visual computing for industry, biomedicine, and art, 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
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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

8 authors.

Haofan Huang *School of Biomedical Engineering, Shenzhen University Medical School, Shenzhen University, Shenzhen, 518060, China.ORCID http://orcid.org/0000-0002-8341-1774
Han Zhou *Radiology Department, Second Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong Province, 515041, China.
Kaibin Huang *School of Biomedical Engineering, Shenzhen University Medical School, Shenzhen University, Shenzhen, 518060, China.
Jie YangDepartment of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong, SAR, China.
Peixi YingDepartment of Ophthalmology, Zhujiang Hospital of Southern Medical University, (The Second Clinical Medical College), Guangzhou, Guangdong Province, 510282, China.
Puxiang LaiDepartment of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong, SAR, China. puxiang.lai@polyu.edu.hk.ORCID http://orcid.org/0000-0003-4811-2012
Yan LinRadiology Department, Second Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong Province, 515041, China. 994809889@qq.com.
Yi GaoSchool of Biomedical Engineering, Shenzhen University Medical School, Shenzhen University, Shenzhen, 518060, China. gaoyi@szu.edu.cn.

Funding

Guangdong Provincial Key Laboratory of Mathematical and Neural Dynamical Systems 2024B1212010004Guangzhou Science and Technology Projects 2025B01J3013, 2025B03J0097Hong Kong Research Grant Council 15125724Innovation and Technology Commission - Hong Kong MHP/206/24National Natural Science Foundation of China 82330061Shenzhen Natural Science Fund 20220810144949003Shenzhen Science and Technology Innovation Commission JCYJ20220818100202005Shenzhen Science and Technology Program grant JCYJ20250604182556073
6 · The paper itself

Abstract

Breast cancer exhibits significant spatiotemporal heterogeneity. Traditional radiomics approaches usually rely on low-temporal-resolution imaging and discrete image phases, failing to capture the rapid and continuous kinetic evolution within the tumor microenvironment. Although ultrafast dynamic contrast-enhanced magnetic resonance imaging captures precise contrast agent permeation, current methodologies lack systematic, dedicated computational frameworks to extract these high-dimensional dynamic features. To bridge this gap, this study developed and validated a robust two-stage spatiotemporal radiomics framework for high-dimensional feature selection and predictive modeling. First, a novel gradient-dynamics-based feature selection algorithm was designed to robustly identify highly discriminative kinetic trajectory patterns and overcome the dimensionality curse of time-series data. Second, a lightweight Transformer-based predictive network incorporating a self-attention knowledge distillation mechanism was deployed to capture deep representational knowledge and enhance the differentiation between benign and malignant lesions. Experimental results demonstrated that the proposed framework outperformed traditional baseline models using delta features or pharmacokinetic parameters, achieving an area under the curve of 0.959 ± 0.022 and an accuracy of 92%, an 8% improvement over conventional temporal radiomics models (P < 0.05). Furthermore, through the visualization of attention heat maps, the model provides highly interpretable evidence of the critical enhancement phases and spatiotemporal evolutionary patterns that drive model decisions. This framework introduces a viable, visually interpretable, and quantitative tool for characterizing tumor heterogeneity, demonstrating its potential to assist in personalized clinical decision-making for breast cancer.

Indexed as

Breast cancerDeep learningKnowledge distillationPrecision medicineSpatiotemporal radiomicsTumor heterogeneity

Identifiers

PMID42690533
PMCPMC13542040

What OpenQuestion holds

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Registered trials

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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.