A Practical Machine Learning Model for Predicting Neoadjuvant Response in HER2-Positive Breast Cancer
María Azmat1, Lucía Graña-López2,3, Manuel Fernández-Delgado1
1Centro Singular de Investigación en Tecnoloxías Intelixentes da USC (CiTIUS), Universidade de Santiago de Compostela, 15705 Santiago de Compostela, Spain.
Diagnostics (Basel, Switzerland)
|August 13, 2026
Summary
Machine learning models can predict pathological complete response in HER2-positive breast cancer using routine clinical and MRI data. This approach aids in pre-treatment risk assessment for better patient management.
Area of Science:
- Oncology
- Radiology
- Machine Learning
Background:
- Pathological complete response (pCR) is a key prognostic marker for HER2-positive breast cancer (BC) after neoadjuvant chemotherapy (NAC).
- Predicting NAC response using pre-treatment data is challenging due to limited reliable predictors.
- This study explores machine learning (ML) for predicting NAC response based on routinely available clinical and MRI data.
Purpose of the Study:
- To evaluate the efficacy of clinicopathologic and baseline MRI variables in predicting NAC response in HER2-positive BC.
- To compare seventy classical ML classifiers for their ability to predict pCR.
Main Methods:
- Retrospective analysis of 112 HER2-positive BC patients treated with NAC.
- Evaluation of 14 pre-treatment variables including hormone receptor status, tumor grade, Ki67, nodal status, and baseline MRI features.
- Comparison of 70 ML classifiers using leave-one-out cross-validation (LOOCV) and performance metrics like accuracy and AUROC.
Main Results:
- A support vector machine (SVM) with a radial basis function (RBF) kernel achieved the highest accuracy (82.1%) and AUROC (83.3%).
- Key predictors included hormone receptor (PR, ER) status, Ki67, and baseline MRI characteristics.
- The ML model demonstrated meaningful predictive performance using routinely available pre-treatment data.
Conclusions:
- Machine learning shows promise in predicting pCR for HER2-positive BC before treatment initiation.
- The approach can potentially enhance pre-treatment clinical risk assessment using existing data.
- Further validation through prospective multicentre studies is necessary for clinical implementation.
