Radiomic Characterization of Breast Tissue from Breast CT Images Obtained with Synchrotron Beams.

Background/Objective: Radiomics offers a powerful, non-invasive approach for extracting quantitative features to predict lesion phenotypes. This study performs a radiomic characterization of breast tissue using synchrotron radiation breast computed tomography (SR-bCT). Method: Four mastectomy samples were imaged at the Australian Synchrotron (ANSTO) using five energies (25, 32, 35, 40, and 60 keV). From 10 slices per energy for each sample, 1546 regions of interest (ROIs) were extracted across four tissue subtypes: fatty, glandular, fibrous, and microcalcified. Using Pyradiomics, 93 features were initially calculated and then reduced to 34, eliminating highly correlated variables to reduce redundancies. Seven linear regression models and a discriminant analysis evaluated subtype tissue separation and radiomic characterization across individuals and combined samples and energies with a good fit (0.81 ≤ R ≤ 0.98). Results: The study identified six possible robust exploratory candidate features independent of sample variability and energy levels, whose mean values are significantly different among the four tissue subtypes (clusters, p < 0.001). The selected candidate features were 90th Percentile, Kurtosis, Skewness, GLCM IDM, GLDM LDE, and NGTDM Coarseness. These metrics successfully differentiated all tissue pairs (microcalcifications/fat, microcalcifications/gland, microcalcifications/fiber, fat/gland, fat/fiber and gland/fiber), with p < 0.05 inside the most general regression model and p < 0.0001 with the linear discriminant separation in clusters. Conclusions: Findings indicate that some first-order and second-order texture metrics reflecting global dependencies remain stable across experimental conditions. Conversely, fine-texture metrics are highly sensitive to sample energy changes, limiting their generalizability. These results align with successful biomarkers in mammography and validate the potential of radiomics in SR-bCT characterization.