Medical physics · 2026
Towards quality control and harmonization of deep learning CT radiomics: An in-silico feasibility study with virtual colorectal liver metastases.
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Venugopal Mamatha, Ramani Sathish, Peoples Jacob J, Do Richard K G, Simpson Amber L, Wang Ge, De Man Bruno
Аннотация
BACKGROUND: Radiomic imaging biomarkers are increasingly studied in oncology as a means to support disease prognosis and personalized treatment planning. While deep learning (DL) offers scalable alternatives to handcrafted radiomic features, DL-derived biomarkers are sensitive to variations in image acquisition protocols and scanner hardware-even within a single imaging modality. To ensure reliable and reproducible biomarker estimation, it is essential to (1) provide clinicians with quantitative uncertainty estimates associated with biomarker predictions, and (2) address acquisition-induced variability through harmonization strategies that render consistent performance across diverse imaging conditions.
PURPOSE: To evaluate uncertainty estimation as a reliability metric for biomarker prediction and to assess the role of image harmonization in improving cross-scanner inference, we develop deep learning radiomics (DLR) models for joint estimation of biomarkers and associated uncertainties and apply linear harmonization filters to standardize imaging conditions.
METHODS: We constructed hybrid digital phantoms by embedding 20,000 virtual colorectal liver metastases into 20 clinical CT liver images to generate metastases-laden simulated scans. The proposed DLR models jointly estimated a selected set of biomarkers and their associated aleatoric uncertainties from simulated images. Models were trained, validated, and tested using a 70:20:10 data split. Variability in CT image acquisition was modelled using two scanner types, two reconstruction kernels, and three x-ray tube current settings. DLR performance was evaluated under direct inference (matched training and test scanners), cross-scanner inference, and harmonized inference using linear harmonization filters. Quantitative evaluation was based on correlation coefficients and root mean squared errors (RMSEs).
RESULTS: The estimated uncertainties were consistently higher for biomarker predictions with larger deviations from ground truth. Excluding high-uncertainty predictions improved concordance between predictions and ground truth biomarkers. The proportion of uncertain predictions increased under cross-scanner inference relative to direct inference, indicating reduced biomarker reliability under heterogeneous imaging conditions. Furthermore, application of harmonization filters reduced RMSEs by an average of 43% across biomarkers and experiments during cross-scanner inference, demonstrating improved cross-scanner consistency.
CONCLUSIONS: In this controlled in-silico study, uncertainty estimation provided a practical reliability metric for DL-based radiomic biomarker prediction, while image harmonization improved reproducibility across heterogeneous acquisition conditions. These findings demonstrate methodological feasibility within a simulation-based framework but have not yet been validated on clinical CT data, motivating future clinical validation and translation.
PURPOSE: To evaluate uncertainty estimation as a reliability metric for biomarker prediction and to assess the role of image harmonization in improving cross-scanner inference, we develop deep learning radiomics (DLR) models for joint estimation of biomarkers and associated uncertainties and apply linear harmonization filters to standardize imaging conditions.
METHODS: We constructed hybrid digital phantoms by embedding 20,000 virtual colorectal liver metastases into 20 clinical CT liver images to generate metastases-laden simulated scans. The proposed DLR models jointly estimated a selected set of biomarkers and their associated aleatoric uncertainties from simulated images. Models were trained, validated, and tested using a 70:20:10 data split. Variability in CT image acquisition was modelled using two scanner types, two reconstruction kernels, and three x-ray tube current settings. DLR performance was evaluated under direct inference (matched training and test scanners), cross-scanner inference, and harmonized inference using linear harmonization filters. Quantitative evaluation was based on correlation coefficients and root mean squared errors (RMSEs).
RESULTS: The estimated uncertainties were consistently higher for biomarker predictions with larger deviations from ground truth. Excluding high-uncertainty predictions improved concordance between predictions and ground truth biomarkers. The proportion of uncertain predictions increased under cross-scanner inference relative to direct inference, indicating reduced biomarker reliability under heterogeneous imaging conditions. Furthermore, application of harmonization filters reduced RMSEs by an average of 43% across biomarkers and experiments during cross-scanner inference, demonstrating improved cross-scanner consistency.
CONCLUSIONS: In this controlled in-silico study, uncertainty estimation provided a practical reliability metric for DL-based radiomic biomarker prediction, while image harmonization improved reproducibility across heterogeneous acquisition conditions. These findings demonstrate methodological feasibility within a simulation-based framework but have not yet been validated on clinical CT data, motivating future clinical validation and translation.