Faculty, Staff and Student Publications

Language

English

Publication Date

11-26-2025

Journal

Scientific Reports

DOI

10.1038/s41598-025-25989-z

PMID

41298623

PMCID

PMC12657976

PubMedCentral® Posted Date

11-26-2025

PubMedCentral® Full Text Version

Post-print

Abstract

Despite being the standard-of-care treatment, neoadjuvant therapy (NAT) attains a complete response only in approximately half of the patients with triple negative breast cancer. Thus, methods to predict and optimize patient response to NAT are needed. Previously, we employed patient-specific MRI data to calibrate a biology-based mathematical model that describes cell movement, proliferation, and death due to drug at the tumor level and cell proliferation at an image voxel level. We now extend our approach by using MRI data to group voxels into "habitats" whereby tumor cells of a habitat share the same proliferation. With this approach, we now calibrate habitat-informed proliferation rates for each habitat rather than local proliferation rates. When comparing error in tumor cell number and volume at the time of calibration, the local calibration has significantly (p <  0.05) lower error than the habitat-informed calibration. However, the habitat-informed predictions of a future timepoint have significantly lower error than the local predictions. Compared to the local calibration, the habitat-informed calibration also requires fewer parameters, reducing the calibration time by a factor of 17. These results suggest that a habitat-informed calibration can provide both accurate and efficient predictions of breast cancer response to NAT.

Keywords

Triple Negative Breast Neoplasms, Humans, Neoadjuvant Therapy, Female, Magnetic Resonance Imaging, Cell Proliferation, Models, Biological, Treatment Outcome, Breast cancer, Computational science, Computational models, Chemotherapy, Magnetic resonance imaging, Cancer

Published Open-Access

yes

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