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Ryan J. Sanford

Publications and source records attributed to Ryan J. Sanford.

2 recordsLinked to original sources

An Uncertainty-Guided Digital Twin Framework for Online Adaptive Proton Therapy in Head and Neck Cancer: A Feasibility Study

Objective: Head and neck (HN) proton therapy spans six to seven weeks of anatomical change, while offline replanning takes about a week. We present an uncertainty-guided digital twin (UGDT) framework that forecasts treatment-day anatomy before treatment and evaluate whether it generates online adaptive proton therapy (APT) plans of clinical quality. Approach: A library of 302 longitudinal deformations from 88 previously treated HN patients was transported onto each new patient's treatment planning CT (TPCT) using two-step multi-atlas deformable image registration (DIR) built on a pretrained CT foundation model, generating about 284 predicted CTs (pdCTs) with contours per patient. Dispersion of propagated clinical target volume (CTV) contours defined a patient-specific robust margin. In ten patients, the quality assurance CT (QACT) triggering a replan represented treatment-day anatomy, and the physician-approved replan was the baseline. The pdCT most similar to the QACT (pdCT-H) and one from the lowest quartile (pdCT-L) were planned to within about 5% of baseline plan quality, forward-calculated on the QACT, and reoptimized to generate online APT plans. Main results: pdCT plans scored within -0.7% (pdCT-H) and -1.0% (pdCT-L) of baseline. Forward calculation on QACT reduced high-dose CTV D98% to 88.3% and 85.5%. After online reoptimization, D98% recovered to 98.3 +/- 0.3% and 98.2 +/- 0.3%, versus 98.5 +/- 0.4% at baseline. Spinal cord and brainstem doses remained below tolerance, and plan quality scores were within -1.1% (p = 0.19) and -1.7% (p = 0.01) of baseline. Significance: UGDT generated online APT plans comparable in quality to physician-approved offline replans using anatomy forecast before treatment, enabling a transition from reactive offline replanning toward anticipatory online adaptation.

physics.med-ph↗

MRI super-resolution in ten sampling steps using a diffusion bridge model

Objective. MRI provides excellent soft-tissue contrast, but long acquisition times can cause patient discomfort and lead to motion artifacts, forcing a trade-off between spatial resolution and scan time. Diffusion-based super-resolution (SR) reconstructs high-resolution (HR) images from low-resolution (LR) inputs, but typically needs many sampling steps and initializes from a Gaussian prior ill-suited to image restoration. We developed an efficient diffusion framework that reconstructs HR MRI directly from LR data. Approach. We propose super-resolution diffusion bridge model (SR-DBM), a super-resolution diffusion bridge model that casts SR as a stochastic transport between the LR and HR image distributions. Through a Doob's h-transform of a mean-reverting stochastic differential equation, SR-DBM pins the process to the paired HR and LR images at its endpoints, initializing reconstruction from the measured anatomy rather than from Gaussian noise. The HR image is recovered by a deterministic reverse trajectory in which a network predicts the clean image at each of only ten sampling steps. We evaluated SR-DBM on ultra-high-field 7T brain T1 MP2RAGE maps and pelvic T2-weighted prostate images against nine comparison methods using PSNR, SSIM, GMSD, and LPIPS. Main results. SR-DBM attained the highest PSNR and SSIM and the lowest GMSD on both datasets (brain: 27.66+-1.52 dB, 0.96+-0.02, 7.96+-1.86$; prostate: 27.87+-2.29 dB, 0.80+-0.05, 8.38+- 1.44), with statistically significant gains over every comparison method (two-sided Wilcoxon signed-rank test with Holm correction, p<0.05). The strongest baseline, SR-EMamba, ranked second. Qualitatively, SR-DBM produced the smallest residual errors and best preserved fine structures and lesions.

cs.CV↗