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一种用于将 TrueBeam 放射治疗系统的治疗计划参数化到 TOPAS 参数控制文件中,以便进行蒙特卡罗模拟的接口工具。

An interface tool to parametrize treatment plans for the TrueBeam radiotherapy system into TOPAS parameter control files for Monte Carlo simulation.

机构信息

University of California San Francisco, Department of Radiation Oncology 1600 Divisadero Street, San Francisco, CA 94143, United States.

Varian, A Siemens Healthineers Company, 3100 Hansen Way, Palo Alto CA 94034, United States.

出版信息

Phys Med. 2024 Aug;124:104485. doi: 10.1016/j.ejmp.2024.104485. Epub 2024 Jul 25.

DOI:10.1016/j.ejmp.2024.104485
PMID:39059251
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11323898/
Abstract

PURPOSE

The Monte Carlo (MC) method, the gold standard method for radiotherapy dose calculations, is underused in clinical research applications mainly due to computational speed limitations. Another reason is the time-consuming and error prone conversion of treatment plan specifications into MC parameters. To address this issue, we developed an interface tool that creates a set of TOPAS parameter control files (PCF) from information exported from a clinical treatment planning system (TPS) for plans delivered by the TrueBeam radiotherapy system.

METHODS

The interface allows the user to input DICOM-RT files, exported from a TPS and containing the plan parameters, and choose different multileaf-collimator models, variance reduction technique parameters, scoring quantities and simulation output formats. Radiation sources are precomputed phase space files obtained from Varian. Based on this information, ready-to-run TOPAS PCF that incorporate the position and angular rotation of the TrueBeam dynamic collimation devices, gantry, couch, and patient according to treatment plan specifications are created.

RESULTS

Dose distributions computed using these PCF were compared against predictions from commercial TPS for different clinical treatment plans and techniques (3D-CRT, IMRT step-and-shoot and VMAT) to evaluate the performance of the interface. The agreement between dose distributions from TOPAS and TPS (>98 % pass ratio in the gamma test) confirmed the correct parametrization of treatment plan specifications into MC PCF.

CONCLUSIONS

This interface tool is expected to widen the use of MC methods in the clinical medical physics field by facilitating the straightforward transfer of treatment plan parameters from commercial TPS into MC PCF.

摘要

目的

蒙特卡罗(MC)方法是放射治疗剂量计算的金标准方法,但在临床研究应用中并未得到广泛应用,主要原因是计算速度受限。另一个原因是将治疗计划规范转换为 MC 参数既耗时又容易出错。为了解决这个问题,我们开发了一个接口工具,该工具可根据从临床治疗计划系统(TPS)导出的信息,为 TrueBeam 放射治疗系统交付的计划创建一组 TOPAS 参数控制文件(PCF)。

方法

该接口允许用户输入从 TPS 导出的包含计划参数的 DICOM-RT 文件,并选择不同的多叶准直器模型、变分减少技术参数、评分量和模拟输出格式。射线源是从瓦里安预先计算的相位空间文件。基于这些信息,根据治疗计划规范,创建包含 TrueBeam 动态准直设备、龙门架、治疗床和患者位置和角度旋转的可运行 TOPAS PCF。

结果

使用这些 PCF 计算的剂量分布与来自商业 TPS 的预测值进行了比较,涉及不同的临床治疗计划和技术(3D-CRT、IMRT 分步和 VMAT),以评估接口的性能。TOPAS 和 TPS 的剂量分布之间的一致性(伽马测试中超过 98%的通过率)证实了将治疗计划规范正确参数化为 MC PCF。

结论

该接口工具有望通过方便地将商业 TPS 的治疗计划参数直接传输到 MC PCF,从而在临床医学物理领域扩大 MC 方法的应用。

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