使用商用合成CT发生器开发用于脑和头颈部肿瘤患者的仅磁共振放射治疗计划工作流程。

Martin Buschmann, Harald Herrmann, Manuela Gober, Aleksandra Winkler, Nicole Eder-Nesvacil, Franziska Eckert, Joachim Widder, Dietmar Georg, Petra Trnková
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引用次数: 0

摘要

背景:在仅磁共振(MR)放射治疗(RT)工作流程中,需要合成计算机断层扫描图像(sCT)作为剂量计算的替代。商业和认证的sCT算法最近可用,但许多尚未在临床环境中进行评估,特别是在头颈部肿瘤(HN)区域。在这项研究中,使用商用sCT发生器在脑和HN体部位进行光子束治疗的mri工作流程在剂量计算精度、固定装置建模以及自动分割的可用性方面进行了评估。方法:回顾性收集13例脑癌和10例HN癌患者的T1W mDIXON序列mri扫描结果。4例和所有HN患者在RT治疗体位用固定装置进行脑部扫描。使用MRCAT算法(Philips, Eindhoven, Netherlands)将所有mri转换为sCT。所有患者均行标准计划CT (pCT)进行临床分割和VMAT治疗计划。将sCT严格注册到pCT,并将临床轮廓转移到sCT。对于基于剂量计算的sCT剂量学评估,在sCT上重新计算所有VMAT计划。pCT和sCT之间所有结构的D1%和Dmean比较,但仅靶的D95%和D98%比较。对于磁共振不可见RT固定装置建模,将磁共振可见标记物置于sCT中,并基于相同的靶剂量-体积参数进行几何稳健性分析。对于危险器官(OARs)的自动分割,pCT和sCT都使用临床建立的基于ct的自动轮廓软件进行自动分割。通过相似剂量-体积参数、骰子相似度(DSC)和Hausforff距离(HD)分析pCT和sCT轮廓的一致性。结果:sCT和pCT包括固定模型的剂量学参数的总体中位偏差(±四分位数范围)为:脑靶体积1.1 ± 0.4%,脑OAR 1.3 ± 1.2%,HN靶体积0.4 ± 0.7%,HN OAR 0.4 ± 0.9%。与pCT自动轮廓相比,所有sCT自动轮廓的中位几何一致性导致脑OAR的DSC = 0.82,HN OAR的DSC = 0.79。结论:采用MRCAT软件包进行脑及HN肿瘤的MR-only RT规划是可行的,临床准确性可接受。磁共振不可见固定装置可以在规划系统中建模,利用基于ct的自动分割工具对sct进行自动分割是可行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of an MR-only radiotherapy treatment planning workflow using a commercial synthetic CT generator for brain and head & neck tumor patients.

Background: In magnetic resonance (MR)-only radiotherapy (RT) workflows, synthetic computed tomography images (sCT) are needed as a surrogate for a dose calculation. Commercial and certified sCT algorithms became recently available, but many have not been evaluated in a clinical setting, especially in the head and neck tumor (HN) region. In this study, an MRI-only workflow using a commercial sCT generator for photon beam therapy in brain and HN body sites was evaluated in terms of dose calculation accuracy, modelling of immobilization devices, as well as usability for autosegmentation.

Methods: For 13 brain and 10 HN cancer patients, MR scans using T1W mDIXON sequences were retrospectively collected. Four brain and all HN patients were scanned in RT treatment position with immobilization devices. All MRIs were converted to a sCT using the MRCAT algorithm (Philips, Eindhoven, The Netherlands). All patients underwent standard planning CT (pCT) for clinical segmentation and VMAT treatment planning. The sCT was rigidly registered to the pCT and clinical contours were transferred to the sCT. For dosimetric evaluation of sCT based dose calculation, all VMAT plans were recalculated on the sCT. D1% and Dmean were compared for all structures between pCT and sCT, but D95%, D98% for targets only. For MR-invisible RT immobilization device modelling, MR-visible markers were placed into sCT and a geometric robustness analysis was performed based on the same target dose-volume parameters. For organs-at-risk (OARs) autosegmentation, both pCT and sCT were autosegmented with a clinically established CT-based autocontouring software. The agreement of contours on pCT and sCT was analyzed by similar dose-volume parameters and dice similarity (DSC) and Hausforff distance (HD).

Results: The overall median deviation (± interquartile range) of dosimetric parameters between sCT and pCT including the immobilization model was 1.1 ± 0.4% for brain target volumes, 1.3 ± 1.2% for brain OAR, 0.4 ± 0.7% for HN target volumes and 0.4 ± 0.9% for HN OAR. The median geometric agreement over all sCT autocontours compared to pCT autocontours resulted in DSC = 0.82 for brain OAR and DSC = 0.79 for HN OAR.

Conclusion: MR-only RT planning using MRCAT software package was feasible for brain and HN tumors, with acceptable clinical accuracy. The MR-invisible immobilization devices could be modelled in the planning system and the autosegmentation on sCTs using a CT-based autosegmentation tool was feasible.

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