ArticleRadiology. Artificial intelligence2025
Prediction of Early Neoadjuvant Chemotherapy Response of Breast Cancer through Deep Learning-based Pharmacokinetic Quantification of DCE MRI.
Article in Radiology. Artificial intelligence, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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4 citing papers in PubMed.
- Beyond pCR Prediction: Subtype-Specific Artificial Intelligence for Treatment Tailoring in Breast Cancer Neoadjuvant Therapy.Cancers · 2026Review
- Lightweight Transformer-based knowledge distillation framework for high-dimensional spatiotemporal radiomics in breast cancer risk prediction.Visual computing for industry, biomedicine, and art · 2026Article
- The role of radiomics in predicting the response to neoadjuvant chemotherapy for breast cancer.Cancer biology & medicine · 2026Review
- From Voxel-wise Fitting to Generative Translation: A Path for Quantitative DCE MRI Analysis in Breast Cancer.Radiology. Imaging cancer · 2026Article
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Abstract
Purpose To improve the generalizability of pathologic complete response prediction following neoadjuvant chemotherapy using deep learning-based retrospective pharmacokinetic quantification of early treatment dynamic contrast-enhanced MRI. Materials and Methods This multicenter retrospective study included breast MRI data from four publicly available datasets of patients with breast cancer acquired from May 2002 to November 2016. Pharmacokinetic quantification was performed using a previously developed deep learning model for clinical multiphasic dynamic contrast-enhanced MRI datasets. Radiomic analysis was performed on pharmacokinetic quantification maps and conventional enhancement maps. These data, together with clinicopathologic variables and shape-based radiomic analysis, were subsequently applied for pathologic complete response prediction using logistic regression. Prediction performance was evaluated by area under the receiver operating characteristic curve (AUC). Results A total of 1073 female patients with breast cancer were included. The proposed method showed improved consistency and generalizability compared with the reference method, achieving higher AUC values across external datasets (0.82 [95% CI: 0.72, 0.91], 0.75 [95% CI: 0.71, 0.79], and 0.77 [95% CI: 0.66, 0.86] for datasets A2, B, and C, respectively). For dataset A2 (from the same study as the training dataset), there was no significant difference in performance between the proposed method and reference method (
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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.