Predicting the response of I-SPY 2 breast cancer patients to treatment using a biology-based mathematical model calibrated with quantitative MRI

Motivation: Optimizing treatment to improve outcomes necessitates a robust tool to accurately predict breast cancer response on a patient-specific basis. Goal(s): We are applying our biology-based mathematical model to I-SPY 2 breast cancer patients to test if its predictive ability generalizes to multi-site data. Approach: Quantitative contrast-enhanced and diffusion-weighted MRI data collected early during treatment were used to calibrate a mathematical model describing tumor cell movement, proliferation, and response. After calibration, the model predicts tumor status after the treatment regimen. Results: The concordance correlation coefficient between the measured and predicted 9-week change was 0.91 for tumor cellularity and 0.88 for tumor volume. Impact: The high degree of agreement between measured and predicted changes in tumor cellularity and volume in the I-SPY 2 dataset indicates that our biology-based mathematical model can potentially make accurate predictions using MRI data from multiple clinical sites.

Authors

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
2024-11-26
DOI
https://doi.org/10.58530/2024/1168
Primary Topic
Mathematical Biology Tumor Growth
Type
article
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article

Predicting the response of I-SPY 2 breast cancer patients to treatment using a biology-based mathematical model calibrated with quantitative MRI

Gaiane M. Rauch, Chengyue Wu, Thomas E. Yankeelov, Rania M. Mohamed 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
Mathematical Biology Tumor Growth
article

Predicting the response of I-SPY 2 breast cancer patients to treatment using a biology-based mathematical model calibrated with quantitative MRI

Gaiane M. Rauch, Chengyue Wu, Thomas E. Yankeelov, Rania M. Mohamed, Reema Patel, Casey E. Stowers, Jingfei Ma
article en

Abstract

Motivation: Optimizing treatment to improve outcomes necessitates a robust tool to accurately predict breast cancer response on a patient-specific basis. Goal(s): We are applying our biology-based mathematical model to I-SPY 2 breast cancer patients to test if its predictive ability generalizes to multi-site data. Approach: Quantitative contrast-enhanced and diffusion-weighted MRI data collected early during treatment were used to calibrate a mathematical model describing tumor cell movement, proliferation, and response. After calibration, the model predicts tumor status after the treatment regimen. Results: The concordance correlation coefficient between the measured and predicted 9-week change was 0.91 for tumor cellularity and 0.88 for tumor volume. Impact: The high degree of agreement between measured and predicted changes in tumor cellularity and volume in the I-SPY 2 dataset indicates that our biology-based mathematical model can potentially make accurate predictions using MRI data from multiple clinical sites.

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
Good health and well-being
Openalex Percentile: Top 77%
Mathematical Biology Tumor Growth
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Predicting the response of I-SPY 2 breast cancer patients to treatment using a biology-based mathematical model calibrated with quantitative MRI — Gaiane M. Rauch, Chengyue Wu, 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 (2024) | TGRS Research Map | TGRS