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基于蒙特卡罗的动态 jaws 调强放疗模拟。

Monte Carlo-based simulation of dynamic jaws tomotherapy.

机构信息

Department of Molecular Imaging, Université Catholique de Louvain, Brussels, Belgium.

出版信息

Med Phys. 2011 Sep;38(9):5230-8. doi: 10.1118/1.3626486.

Abstract

PURPOSE

Original TomoTherapy systems may involve a trade-off between conformity and treatment speed, the user being limited to three slice widths (1.0, 2.5, and 5.0 cm). This could be overcome by allowing the jaws to define arbitrary fields, including very small slice widths (<1 cm), which are challenging for a beam model. The aim of this work was to incorporate the dynamic jaws feature into a Monte Carlo (MC) model called TomoPen, based on the MC code PENELOPE, previously validated for the original TomoTherapy system.

METHODS

To keep the general structure of TomoPen and its efficiency, the simulation strategy introduces several techniques: (1) weight modifiers to account for any jaw settings using only the 5 cm phase-space file; (2) a simplified MC based model called FastStatic to compute the modifiers faster than pure MC; (3) actual simulation of dynamic jaws. Weight modifiers computed with both FastStatic and pure MC were compared. Dynamic jaws simulations were compared with the convolution∕superposition (C∕S) of TomoTherapy in the "cheese" phantom for a plan with two targets longitudinally separated by a gap of 3 cm. Optimization was performed in two modes: asymmetric jaws-constant couch speed ("running start stop," RSS) and symmetric jaws-variable couch speed ("symmetric running start stop," SRSS). Measurements with EDR2 films were also performed for RSS for the formal validation of TomoPen with dynamic jaws.

RESULTS

Weight modifiers computed with FastStatic were equivalent to pure MC within statistical uncertainties (0.5% for three standard deviations). Excellent agreement was achieved between TomoPen and C∕S for both asymmetric jaw opening∕constant couch speed and symmetric jaw opening∕variable couch speed, with deviations well within 2%∕2 mm. For RSS procedure, agreement between C∕S and measurements was within 2%∕2 mm for 95% of the points and 3%∕3 mm for 98% of the points, where dose is greater than 30% of the prescription dose (gamma analysis). Dose profiles acquired in transverse and longitudinal directions through the center of the phantom were also compared with excellent agreement (2%∕2 mm) between all modalities.

CONCLUSIONS

The combination of weights modifiers and interpolation allowed implementing efficiently dynamic jaws and dynamic couch features into TomoPen at a minimal cost in terms of efficiency (simulation around 8 h on a single CPU).

摘要

目的

原始的 TomoTherapy 系统在适形性和治疗速度之间可能存在权衡,用户只能选择三种叶片宽度(1.0、2.5 和 5.0cm)。通过允许机架定义任意野,包括对束流模型具有挑战性的非常小的叶片宽度(<1cm),可以克服这一问题。本研究的目的是将动态机架功能整合到基于 MC 代码 PENELOPE 的 MC 模型 TomoPen 中,该模型之前已针对原始 TomoTherapy 系统进行了验证。

方法

为了保持 TomoPen 的整体结构及其效率,该模拟策略采用了以下几种技术:(1)使用仅 5cm 相空间文件来计算权重修正值,以适应任何机架设置;(2)基于 MC 的简化模型 FastStatic 用于比纯 MC 更快地计算修正值;(3)实际模拟动态机架。比较了使用 FastStatic 和纯 MC 计算的权重修正值。在奶酪体模中,对于两个目标沿纵向间隔 3cm 的计划,比较了动态机架模拟与 TomoTherapy 的卷积/叠加(C∕S)。在两种模式下进行了优化:不对称机架-恒速机架(“运行开始停止”,RSS)和对称机架-变速机架(“对称运行开始停止”,SRSS)。对于 RSS 程序,还使用 EDR2 胶片进行了 RSS 的测量,以对具有动态机架的 TomoPen 进行正式验证。

结果

FastStatic 计算的权重修正值在统计不确定度内(三个标准差内为 0.5%)与纯 MC 相当。对于不对称机架开口/恒速机架和对称机架开口/变速机架,TomoPen 与 C∕S 之间的吻合度非常好,偏差均在 2%∕2mm 以内。对于 RSS 程序,C∕S 与测量值之间的吻合度在 95%的点上为 2%∕2mm,在 98%的点上为 3%∕3mm,其中剂量大于处方剂量的 30%(伽玛分析)。通过体模中心的横向和纵向方向获得的剂量分布也与所有模态之间的良好吻合度(2%∕2mm)进行了比较。

结论

通过权重修正值和插值的组合,可以在效率方面以最小的成本(单个 CPU 上大约 8 小时的模拟)有效地将动态机架和动态机架功能整合到 TomoPen 中。

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