初始化
人工智能
图像配准
计算机科学
校准
相似性(几何)
模式识别(心理学)
磁共振成像
核医学
匹配(统计)
贝叶斯概率
辍学(神经网络)
概率逻辑
蒙特卡罗方法
放射治疗
深度学习
Sørensen–骰子系数
肺癌
计算机视觉
贝叶斯定理
差异(会计)
医学
医学影像学
数学
放射科
平均绝对误差
放射治疗计划
作者
Chengtao Wei,Domagoj Radonic,Rabea Klaar,Natascha Hohmann,Sebastian Norbert Marschner,Chukwuka Eze,Sina Mansoorian,Stefanie Corradini,Claus Belka,Guillaume Landry,Moritz Rabe,Christopher Kurz
标识
DOI:10.1088/1361-6560/aebc09
摘要
Abstract Objective . To develop a deep learning (DL) based probabilistic 3D deformable image registration framework for uncertainty-aware dose accumulation in magnetic resonance imaging-guided radiotherapy of lung cancer. Approach . We propose TransMorph-prob (TM-prob), a variational Bayesian model that predicts the voxel-wise mean and variance of dense displacement fields (DDFs). Two TM-prob models were trained on an internal computed tomography dataset (725 patients) and a low-field MR-linac dataset (102 patients), and benchmarked against Monte Carlo dropout TransMorph (TM-MCD) and DIRUncertainty with B-spline initialization (ASDIR) on the deformable image registration laboratory (DIRLAB) 4DCT dataset (10 patients, 3000 landmarks), and an annotated MR-linac dataset (16 patients, 107 image pairs, 227 landmarks) with target and seven organ-at-risk contours. Both datasets contained an additional 1239/13 289 algorithm-generated landmarks. Performance was evaluated using target registration error (TRE), Dice similarity coefficient (DSC), landmark- and voxel-wise expected calibration errors (LECE/ECE), and dose distributions derived from 2000 DDF samples per patient. Main results . On the DIRLAB dataset, TM-prob achieved a median TRE of 1.8 mm/2.8 mm on manual/algorithm-generated landmarks, versus 1.3 mm/2.4 mm for ASDIR and 2.1 mm/3.0 mm for TM-MCD. On the MRI dataset, TM-prob achieved the median TRE of 3.9 mm/2.6 mm and a mean DSC of 0.87, matching ASDIR (3.3 mm/2.7 mm, and DSC of 0.87) while outperforming TM-MCD (4.4 mm/2.9 mm, and 0.84). In uncertainty calibration, TM-prob achieved a LECE of 1.74 mm/0.30 mm on MRI manual/algorithm-generated landmarks versus 2.41 mm/0.56 mm for ASDIR and 6.65 mm/3.92 mm for TM-MCD, and an average contour ECE of 5.8% versus 7.0% and 21.2%. Two patients with indistinct gross tumor volume boundaries exhibited substantially wider target D95 distributions, demonstrating that calibrated DDF uncertainty translates into clinically relevant dose-coverage uncertainty. Significance . TM-prob is an end-to-end DL model, achieving fast, well-calibrated, uncertainty-aware registration for lung cancer patients, enabling reliable DDF uncertainty propagation into dose accumulation for clinical decision-making in online adaptive radiotherapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI