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Breast cancers are classified according to the expression of estrogen, progesterone, and HER2 receptors. In the absence of these biomarkers, the cancer is characterized as triple-negative breast cancer (TNBC), which does not respond to targeted therapies. Therefore, strategies to enhance immunotherapy are required, particularly given that radiotherapy can modulate the tumor microenvironment by increasing immune cell levels.
We utilized tumor volume data to develop a calibration and model selection framework for mathematical models based on ordinary differential equations (ODEs), employing a Bayesian approach. The investigations used 4T1 cells as a model for TNBC, which exhibited distinct radiation response profiles (sensitivity and resistance). The experimental design involved 56 mice distributed into six groups: control (sensitive and resistant cells without treatment), radiotherapy (sensitive and resistant cells), immunotherapy (sensitive cells), and a combination of radiotherapy and immunotherapy (sensitive cells).
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