Key result
ChemoCardioNet predicts chemotherapy-induced cardiotoxicity with an AUC of 0.92, beating traditional machine learning models.
Why the study?
Chemotherapy-induced cardiotoxicity remains a major cause of morbidity and mortality among cancer survivors, and conventional monitoring often fails to detect early subclinical cardiac injury.
Does the ChemoCardioNet multimodal deep learning framework improve the early prediction of chemotherapy-induced cardiotoxicity compared to traditional machine learning approaches in patients undergoing chemotherapy?
Cohort (n=1,200)
Does the ChemoCardioNet multimodal deep learning framework improve the early prediction of chemotherapy-induced cardiotoxicity compared to traditional machine learning approaches in patients undergoing chemotherapy?
Effect estimate: AUC 0.92
A novel multimodal deep learning framework, ChemoCardioNet, accurately predicts chemotherapy-induced cardiotoxicity earlier than conventional echocardiographic monitoring, potentially improving cardio-oncology care.
May support earlier cardiotoxicity stratification in chemotherapy; extends prior ML models but leaves open prospective outcome impact.
Chemotherapy-induced cardiotoxicity (CIC) remains a major cause of morbidity and mortality among cancer survivors, and conventional monitoring often fails to detect early subclinical cardiac injury. We propose ChemoCardioNet, an explainable multimodal deep learning framework that predicts cardiotoxicity risk before clinical manifestation by integrating electrocardiograms (ECG), echocardiography, clinical variables, and serum biomarkers. The architecture combines modality-specific encoders, including 1D convolutional transformers for ECG sequences, CNN-ViT hybrid blocks for echocardiographic frames, and multilayer perceptrons for clinical and biomarker features. A cross-attention fusion transformer aligns latent representations across modalities and captures temporal evolution across chemotherapy cycles. The model outputs a probabilistic cardiotoxicity risk score with feature-level explainability using SHAP analysis. In a cohort of 1,200 patients, ChemoCardioNet achieved an AUC of 0.92, outperforming single-modality and traditional machine learning approaches by 8-12%. The model predicted cardiotoxicity approximately two cycles before detectable echocardiographic dysfunction, supporting earlier risk identification and improved cardio-oncology monitoring.
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Sarada Prasad Dakua (2026) conducted a cohort in Chemotherapy-induced cardiotoxicity (n=1,200). ChemoCardioNet vs. Single-modality and traditional machine learning approaches was evaluated on Cardiotoxicity risk prediction (AUC 0.92). ChemoCardioNet predicted chemotherapy-induced cardiotoxicity with an AUC of 0.92, outperforming single-modality and traditional machine learning approaches by 8-12%.
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