Predicting doxorubicin-induced cardiotoxicity in breast cancer: leveraging machine learning with synthetic data
- 1Huna, São Paulo, SP, Brazil. dani@huna-ai.com.
- 2Departamento de Ciência da Computação, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil. dani@huna-ai.com.
- 3Faculdade de Farmàcia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
- 4Faculdade Ciências Médicas de Minas Gerais, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
- 5Instituto de Hipertensão, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
- 6Division of Sleep Surgery, Stanford University School of Medicine, Stanford, CA, USA.
- 7Departamento de Ciência da Computação, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
- 0Huna, São Paulo, SP, Brazil. dani@huna-ai.com.
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View abstract on PubMed
Summary
This summary is machine-generated.A new model predicts Doxorubicin (DOXO) cardiotoxicity in breast cancer patients using routine blood tests and clinical data. This approach aids early identification of at-risk individuals, enabling timely interventions.
Area Of Science
- Oncology
- Cardiology
- Biostatistics
Background
- Doxorubicin (DOXO) chemotherapy is vital for breast cancer treatment.
- DOXO-induced cardiotoxicity affects over 25% of patients, necessitating risk prediction.
- Early identification of susceptible patients allows for alternative treatments or cardioprotective strategies.
Purpose Of The Study
- To develop and validate a predictive model for DOXO-induced cardiotoxicity.
- To assess the efficacy of the Data Augmentation and Smoothing (DAS) method for enhancing small medical datasets.
- To identify key clinical and biomarker predictors of cardiotoxicity.
Main Methods
- Analysis of data from 78 Brazilian breast cancer patients.
- Application of the Data Augmentation and Smoothing (DAS) method to generate 4892 synthetic samples.
- Integration of routine blood biomarkers (CRP, cholesterol profile, hematocrit, hemoglobin) and clinical data (BMI, smoking status).
- Comparison of DAS with ADASYN, SMOTE, and SDV for synthetic data generation.
Main Results
- The predictive model achieved an AUROC of 0.85±0.10, sensitivity of 0.89, and specificity of 0.69.
- The DAS method demonstrated superior performance in synthetic data generation compared to ADASYN, SMOTE, and SDV.
- The model effectively integrated routine blood biomarkers and clinical measures for risk assessment.
Conclusions
- The developed model shows potential as a screening tool for DOXO-induced cardiotoxicity in breast cancer patients.
- The DAS method is a promising technique for generating high-fidelity synthetic medical data, particularly for small sample sizes.
- This study pioneers a specific cardiotoxicity prediction model for DOXO, improving patient management and outcomes.
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