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Chase Ruff

Publications and source records attributed to Chase Ruff.

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Modality-AGnostic Image Cascade (MAGIC) for Multi-Modality Cardiac Substructure Segmentation

Cardiac substructure delineation is emerging in treatment planning to minimize the risk of radiation-induced heart disease. Deep learning offers efficient methods to reduce contouring burden but currently lacks generalizability across different modalities and overlapping structures. This work introduces and validates a Modality-AGnostic Image Cascade (MAGIC) deep-learning pipeline for comprehensive and multi-modal cardiac substructure segmentation. MAGIC is implemented through replicated encoding and decoding branches of an nnU-Net backbone to handle multi-modality inputs and overlapping labels. First benchmarked on the multi-modality whole-heart segmentation (MMWHS) dataset including cardiac CT-angiography (CCTA) and MR modalities, twenty cardiac substructures (heart, chambers, great vessels (GVs), valves, coronary arteries (CAs), and conduction nodes) from clinical simulation CT (Sim-CT), low-field MR-Linac, and cardiac CT-angiography (CCTA) modalities were delineated to train semi-supervised (n=151), validate (n=15), and test (n=30) MAGIC. For comparison, fourteen single-modality comparison models (two MMWHS modalities and four subgroups across three clinical modalities) were trained. Methods were evaluated for efficiency and against reference contours through the Dice similarity coefficient (DSC) and two-tailed Wilcoxon Signed-Rank test (p<0.05). Average MMWHS DSC scores across CCTA and MR inputs were 0.88(0.08) and 0.87(0.04) respectively with significant improvement over unimodal baselines. Average 20-structure DSC scores were 0.75(0.16) for Sim-CT, 0.68(0.21) for MR-Linac, and 0.80(0.16) for CCTA. Furthermore, >80% and >70% reductions in training time and parameters were achieved, respectively. MAGIC offers an efficient, lightweight solution capable of segmenting multiple image modalities and overlapping structures in a single model without compromising segmentation accuracy.

physics.med-ph

Deducing Cardiorespiratory Motion of Cardiac Substructures Using a Novel 5D-MRI Workflow for Radiotherapy

Objective: Cardiotoxicity is a devastating complication of thoracic radiotherapy. Current radiotherapy imaging protocols are insufficient to decouple and quantify cardiac motion, limiting substructure-specific motion considerations in treatment planning. We propose a 5D-MRI workflow for substructure-specific motion analysis, with future extension to margin calculation. Approach: Our 5D-MRI workflow was implemented for 10 healthy volunteers, ranging from 23 to 65 years old, reconstructing images for end-exhale/inhale and active-exhale/inhale for end-systole/diastole. For motion assessment, proximal coronary arteries, chambers, great vessels, and cardiac valves/nodes were contoured across all images and verified. Centroid/bounding box excursion was calculated for cardiac, respiratory, and hysteresis motion. Distance metrics were tested for statistical independence across substructure pairings. Main Results: 5D-MRI images were successfully acquired and contoured for all volunteers. Cardiac motion was greatest for the coronary arteries (specifically the right coronary) and smallest for the great vessels. Respiratory motion was dominant in the S-I direction and largest for the inferior vena cava. Respiratory hysteresis was generally <5 mm but exceeded 5 mm for some volunteers. For cardiac motion, there were statistical differences between the coronary arteries, chambers, and great vessels, and between the right/left heart. Respiratory motion differed significantly between the base and apex of the heart. Significance: Our 5D-MRI workflow successfully decouples cardiorespiratory motion with one ~5-minute acquisition. Cardiac motion was >5mm for the coronary arteries and chambers, while respiratory motion was >5mm for all substructures. Statistical considerations and inter-patient variability indicate a substructure and patient-specific approach may be needed for PRV assessment.

physics.med-ph