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Evaluating dosimetric differences in spine stereotactic body radiotherapy: An international multi-institutional treatment planning study

机译:评估脊柱立体定向放射治疗的剂量学差异:国际多机构治疗计划研究

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IntroductionStereotactic body radiotherapy (SBRT) planning for spinal metastases is a challenging task that involves complex target shapes and steep dose gradients proximal to the spinal cord. The aim of the present study is to investigate dosimetric variability among delivery systems and institutions doing spine SBRT.Materials and Methods: Three institutions (in Japan, Canada, and the USA) participated in this retrospective treatment planning study. Computed tomography (CT) datasets for three patients including fully delineated targets and organs-at-risk (OAR) were distributed to all three institutions for planning. Delivery systems included the Clinac 21EX, Vero4DRT, Synergy S, and CyberKnife. All treatment plans were generated using a prescribed dose of 24 Gy in 2 fractions and met the following objectives: the evaluated planning target volume (PTVevl, defined as the PTV minus spinal cord) should receive greater than 16.8 Gy in at least 95% of the volume (D95 > 16.8 Gy) and a maximum dose to the less than 140% of the prescribed dose (Dmax < 33.6 Gy). The maximum dose of planning risk volume (PRV) cord or thecal sac was limited to 0.035 cm3 receiving less than 17 Gy. Aside from minimum and maximum dose objectives for the PTVevl, there were no criteria regarding the shape of the PTVevl dose-volume histogram (DVH). For each completed treatment plan, the following DVH parameters were evaluated for the PTVevl: D95, D80, D50, D2 and sigma-index (S-index, standard deviation of the differential DVH).
机译:简介立体定向放射疗法(SBRT)规划脊柱转移是一项艰巨的任务,涉及复杂的目标形状和靠近脊髓的陡峭剂量梯度。本研究的目的是调查在进行脊柱SBRT的输送系统和机构之间的剂量学变异性。材料与方法:三个机构(日本,加拿大和美国)参加了这项回顾性治疗计划研究。将三位患者的计算机断层扫描(CT)数据集(包括完全划定的目标和危险器官(OAR))分发给所有三个机构进行规划。交付系统包括Clinac 21EX,Vero4DRT,Synergy S和Cyber​​Knife。所有治疗计划均使用24 Gy的规定剂量分两部分制定,并达到以下目标:评估的计划目标体积(PTVevl,定义为PTV减去脊髓)在至少95%的受试者中应接受大于16.8 Gy的治疗。最大剂量(D95> 16.8 Gy),最大剂量小于规定剂量的140%(Dmax <33.6 Gy)。计划性风险量(PRV)脐带或鞘囊的最大剂量限制为0.035 cm 3 ,且小于17 Gy。除了PTVevl的最小和最大剂量目标外,没有关于PTVevl剂量体积直方图(DVH)形状的标准。对于每个完整的治疗计划,对PTVevl评估以下DVH参数:D95,D80,D50,D2和sigma-index(S-index,差分DVH的标准偏差)。

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