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快速患者特异性乳腺CT剂量测定:蒙特卡罗MGD估计的22倍加速

Fast Patient-Specific Breast CT Dosimetry: 22-Fold Acceleration of Monte Carlo MGD Estimation

Amir Entezam, Ashkan Pakzad, Christopher J. Hall, Anton Maksimenko, Matthew J. Cameron, Adam Round, Seyedamir T. Taba, Keith A. Nugent, Daniel Häusermann, Patrick C. Brennan, Timur E. Gureyev, Harry M. Quiney

arXiv 2609.03263首次发表:更新:

发表机构

The University of Melbourne; Australian Synchrotron, ANSTO; The University of Sydney(墨尔本大学; 澳大利亚同步辐射中心,澳斯特原子能组织; 悉尼大学)

机构由 AI 辅助整理,请以论文原文为准。

AI 中文总结

该研究优化乳腺CT剂量测定的体模分辨率与蒙特卡罗效率,通过各向异性下采样及减少光子历史,实现MGD估计22倍加速,为实时患者特异性乳腺CT剂量测定提供基础。

AI 中文摘要

在乳腺计算机断层扫描(BCT)中,准确的患者特异性平均腺体剂量(MGD)估计需要解剖学真实模型,但高分辨率患者衍生体模对蒙特卡罗(MC)剂量测定带来了高计算需求。我们此前开发并验证了基于EGSnrc的同步加速器传播型相位对比BCT(PB-PCT)框架,用于澳大利亚同步加速器的首个人体研究。随着参与者成像开始,本研究旨在优化体模空间分辨率和MC效率,同时保持MGD准确性,以实现快速患者特异性剂量测定。从在35 keV下获取的乳房切除术标本的PB-PCT图像生成四个具有不同体积和腺体度的患者特异性异质乳腺体模,每个标本的最高分辨率体模作为参考。通过增加平面内体素尺寸和层厚对体模进行下采样,并使用EGSnrc/DOSXYZnrc重新计算MGD,采用与参考MGD相差4.5%作为准确性标准。随后减少初级光子历史以确定可接受MC精度所需的最小值。0.30×0.30×3.00 mm³的公共体素尺寸使所有四个体模的MGD与参考值的偏差保持在4.5%以内,同时减少了约20-31倍的体素数量。MGD对平面内体素尺寸的敏感性高于层厚,支持各向异性下采样。降低分辨率的体模使光子历史减少15倍至2×10⁸,同时保持可接受的统计不确定性。综合优化将计算时间从约1600分钟减少到72分钟,实现22倍加速。患者特异性体模可在保持MGD准确性的同时大幅下采样,显著降低计算负担,该优化为未来实时患者特异性BCT剂量测定奠定了基础。

英文摘要

Accurate patient-specific mean glandular dose (MGD) estimation in breast computed tomography (BCT) requires anatomically realistic models, but high-resolution patient-derived phantoms impose high computational demands on Monte Carlo (MC) dosimetry. We previously developed and validated an EGSnrc-based framework for synchrotron propagation-based phase-contrast BCT (PB-PCT) for the first-in-human study at the Australian Synchrotron. With participant imaging commencing, this study aimed to optimize phantom spatial resolution and MC efficiency while maintaining MGD accuracy, for a rapid patient-specific dosimetry. Four patient-specific heterogeneous breast phantoms with varying volume and glandularity were generated from PB-PCT images of mastectomy specimens acquired at 35 keV. The highest-resolution phantom for each specimen served as the reference. Phantoms were downsampled by increasing in-plane voxel size and slice thickness, and MGD was recalculated using EGSnrc/DOSXYZnrc. A 4.5% difference from reference MGD was adopted as the accuracy criterion. Primary photon histories were then reduced to determine the minimum required for acceptable MC precision. A common voxel size of 0.30 x 0.30 x 3.00 mm3 maintained MGD within 4.5% of reference for all four phantoms while reducing voxel number by approximately 20-31-fold. MGD was more sensitive to in-plane voxel size than slice thickness, supporting anisotropic downsampling. Reduced-resolution phantoms enabled a 15-fold reduction in photon histories to 2 x 10^8 while maintaining acceptable statistical uncertainty. Combined optimization reduced computation time from approximately 1600 to 72 min, a 22-fold acceleration. Patient-specific phantoms can be substantially downsampled while maintaining MGD accuracy and markedly reducing computational burden. This optimization provides a foundation for future real-time patient-specific BCT dosimetry.

论文原文

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