18F-FDG PET/CT-based deep radiomic models for enhancing chemotherapy response prediction in breast cancer
- Zirui Jiang 1, Joshua Low 1, Colin Huang 2, Yong Yue 2, Christopher Njeh 2, Oluwaseyi Oderinde 3,4
- Zirui Jiang 1, Joshua Low 1, Colin Huang 2
- 1Advanced Molecular Imaging in Radiotherapy (AdMIRe) Research Lab, School of Health Sciences, College of Health and Human Sciences, Purdue University, West Lafayette, IN, 47907, USA.
- 2Department of Radiation Oncology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
- 3Advanced Molecular Imaging in Radiotherapy (AdMIRe) Research Lab, School of Health Sciences, College of Health and Human Sciences, Purdue University, West Lafayette, IN, 47907, USA. ooderind@purdue.edu.
- 4Department of Radiation Oncology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA. ooderind@purdue.edu.
- 0Advanced Molecular Imaging in Radiotherapy (AdMIRe) Research Lab, School of Health Sciences, College of Health and Human Sciences, Purdue University, West Lafayette, IN, 47907, USA.
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View abstract on PubMed
Summary
This summary is machine-generated.Deep radiomic models accurately predict breast cancer chemotherapy response after the first cycle. Integrating deep learning features with XGBoost improves early treatment assessment and personalized therapy strategies.
Area Of Science
- Oncology
- Medical Imaging
- Artificial Intelligence
Background
- Accurate prediction of breast cancer chemotherapy response is crucial for personalized treatment.
- Early identification of non-responders can guide therapeutic strategy adjustments.
- Radiomics and deep learning offer potential for enhanced predictive accuracy.
Purpose Of The Study
- To develop and evaluate deep radiomic models for predicting chemotherapy response in breast cancer patients after the first treatment cycle.
- To compare the performance of XGBoost, random forest, logistic regression, and support vector machine models.
- To assess the impact of integrating deep learning-derived features on predictive accuracy.
Main Methods
- Retrospective analysis of 18F-Fludeoxyglucose PET/CT imaging and clinical data from 60 breast cancer patients.
- Extraction of radiomic features from the gross tumor volume (GTV) delineated on PET images.
- Application of a Squeeze-and-Excitation Network (SENet) deep learning model to generate additional features.
- Development and comparison of XGBoost, random forest, logistic regression, and support vector machine models using radiomic and deep learning features.
- Performance evaluation using receiver operating characteristic area under the curve (ROC AUC) and fivefold cross-validation.
Main Results
- The XGBoost model achieved the highest AUC (0.85) using only radiomic features.
- Incorporating deep learning-derived features from SENet significantly improved AUC values for all models (XGBoost: 0.92, RF: 0.88, LR: 0.90, SVM: 0.61).
- The enhanced models enabled early prediction of chemotherapy response based on pre-treatment (T1) and post-first-cycle (T2) imaging data.
Conclusions
- Integrating deep learning-derived features substantially enhances the predictive performance of radiomic models for breast cancer chemotherapy response.
- The XGBoost model, augmented with deep learning features, demonstrates superior capability for early and accurate prediction of treatment outcomes.
- These findings support the potential of advanced radiomic models in optimizing personalized therapeutic strategies for breast cancer patients.
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