Cluster analysis of quantitative ultrafast DCE-MRI for prediction of breast cancer response to neoadjuvant chemotherapy

Motivation: Early prediction of pathologic complete response (pCR) enhances personalized breast cancer treatment. Goal(s): This study aims to measure kinetic parameters from pre-neoadjuvant chemotherapy (NAC) ultrafast dynamic contrast-enhanced (DCE)-MRI using k-means clustering (KMC) to predict pCR. Approach: Fifty-six patients undergoing NAC were enrolled. Tumor and normal parenchymal voxels were divided into five clusters based on maximum enhancement rate. Ipsilateral/contralateral (I/C) background parenchymal enhancement kinetics (kBPE) parameters were compared between pCR and non-pCR patients. A logistic regression model incorporating clinical features. Results: MRI tumor kinetics, and kBPE I/Cs achieved an AUC of 0.94, with 0.91 sensitivity and specificity, for predicting breast cancer response to NAC. Impact: K-means clustering analysis of ultrafast DCE-MRI is a stable technique to effectively predict treatment response in breast cancer patients prior to neoadjuvant chemotherapy, which facilitates personalized therapy adjustments and can improve clinical outcomes through individualized treatments.

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Publication Details

Journal
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Published
2025-09-16
DOI
https://doi.org/10.58530/2025/1987
Primary Topic
MRI in cancer diagnosis
Type
article
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article

Cluster analysis of quantitative ultrafast DCE-MRI for prediction of breast cancer response to neoadjuvant chemotherapy

Rita Nanda, Hiroyuki Abé, Frederick M. Howard, Kirti Kulkarni et al.
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
MRI in cancer diagnosis
article

Cluster analysis of quantitative ultrafast DCE-MRI for prediction of breast cancer response to neoadjuvant chemotherapy

Rita Nanda, Hiroyuki Abé, Frederick M. Howard, Kirti Kulkarni, Gregory S. Karczmar, Xiaobing Fan, Zhen Ren, Nan Chen, Anna Biernacka
article en

Abstract

Motivation: Early prediction of pathologic complete response (pCR) enhances personalized breast cancer treatment. Goal(s): This study aims to measure kinetic parameters from pre-neoadjuvant chemotherapy (NAC) ultrafast dynamic contrast-enhanced (DCE)-MRI using k-means clustering (KMC) to predict pCR. Approach: Fifty-six patients undergoing NAC were enrolled. Tumor and normal parenchymal voxels were divided into five clusters based on maximum enhancement rate. Ipsilateral/contralateral (I/C) background parenchymal enhancement kinetics (kBPE) parameters were compared between pCR and non-pCR patients. A logistic regression model incorporating clinical features. Results: MRI tumor kinetics, and kBPE I/Cs achieved an AUC of 0.94, with 0.91 sensitivity and specificity, for predicting breast cancer response to NAC. Impact: K-means clustering analysis of ultrafast DCE-MRI is a stable technique to effectively predict treatment response in breast cancer patients prior to neoadjuvant chemotherapy, which facilitates personalized therapy adjustments and can improve clinical outcomes through individualized treatments.

Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Openalex Percentile: Top 65%
MRI in cancer diagnosis
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Cluster analysis of quantitative ultrafast DCE-MRI for prediction of breast cancer response to neoadjuvant chemotherapy — Rita Nanda, Hiroyuki Abé, et al. · Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition (2025) | TGRS Research Map | TGRS