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Inter‐ and intrafractional dose uncertainty in hypofractionated Gamma Knife radiosurgery

机译:低分割伽玛刀放射外科手术中的分数间和分数内剂量不确定性

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摘要

The purpose of this study is to evaluate inter‐ and intrafractional dose variations resulting from head position deviations for patients treated with the Extend relocatable frame system utilized in hypofractionated Gamma Knife radiosurgery (GKRS). While previous reports characterized the residual setup and intrafraction uncertainties of the system, the dosimetric consequences have not been investigated. A digital gauge was used to measure the head position of 16 consecutive Extend patients (62 fractions) at the time of simulation, before each fraction, and immediately following each fraction. Vector interfraction (difference between simulation and prefraction positions) and intrafraction (difference between postfraction and prefraction positions) shifts in patient position were calculated. Planned dose distributions were shifted by the offset to determine the time‐of‐treatment dose. Variations in mean and maximum target and organ at risk (OAR) doses as a function of positional shift were evaluated. The mean vector interfraction shift was 0.64 mm (Standard Deviation (SD): 0.25 mm, maximum: 1.17 mm). The mean intrafraction shift was 0.39 mm (SD: 0.25 mm, maximum: 1.44 mm). The mean variation in mean target dose was 0.66% (SD: 1.15%, maximum: 5.77%) for interfraction shifts and 0.26% (SD: 0.34%, maximum: 1.85%) for intrafraction shifts. The mean variation in maximum dose to OARs was 7.15% (SD: 5.73%, maximum: 30.59%) for interfraction shifts and 4.07% (SD: 4.22%, maximum: 17.04%) for intrafraction shifts. Linear fitting of the mean variation in maximum dose to OARs as a function of position yielded dose deviations of 10.58%/mm for interfractional shifts and 7.69%/mm for intrafractional shifts. Positional uncertainties when performing hypofractionated Gamma Knife radiosurgery with the Extend system are small and comparable to frame‐based uncertainties (  1 mm). However, the steep dose gradient characteristics of GKRS mean that the dosimetric consequences of positional uncertainties should be considered as part of treatment planning. These dose uncertainties should be evaluated in the context of tumor response and OAR tolerance for hypofractionated treatment scenarios where any increase in dose may be tempered by the increased protection hypofractionation provides to normal tissue.PACS number(s): 87.52.‐g
机译:这项研究的目的是评估在超分割伽玛刀放射外科(GKRS)中使用可扩展可重定位框架系统治疗的患者因头部位置偏差而引起的分数间和分数内剂量变化。尽管先前的报告对系统的残留设置和内部分数不确定性进行了描述,但剂量学后果尚未得到调查。在模拟时,每个分数之前以及每个分数之后立即使用数字量规测量16位连续Extend患者(62个分数)的头部位置。计算了患者位置的向量分数(模拟和预分数位置之间的差异)和分数内分数(分数和后分数之间的差异)的变化。计划的剂量分布偏移偏移量以确定治疗时间剂量。评估了平均和最大靶标和风险器官(OAR)剂量随位置变化的变化。平均矢量屈光度偏移为0.64 mm(标准偏差(SD):0.25 mm,最大值:1.17 mm)。平均分数内偏移为0.39毫米(标准差:0.25毫米,最大值:1.44毫米)。对于分数移位,平均目标剂量的平均变化为0.66%(标准差:1.15%,最大值:5.77%),对于分数内移位,平均目标剂量的平均偏差为0.26%(标准差:0.34%,最大值:1.85%)。 OARs的最大剂量的平均偏差为fraction shifts的7.15%(SD:5.73%,最大值:30.59%)和fractional intra shifts的平均值为4.07%(SD:4.22%,最大值:17.04%)。线性拟合最大剂量对OARs的平均变化作为位置的函数,对于分数移位,剂量偏差为10.58%/ mm,对于分数移位,剂量偏差为7.69%/ mm。使用Extend系统进行超小尺寸伽马刀放射外科手术时的位置不确定性很小,可以与基于框架的不确定性(<1mm)相媲美。然而,GKRS陡峭的剂量梯度特征意味着位置不确定性的剂量学后果应被视为治疗计划的一部分。这些剂量不确定性应在低分数治疗情况下的肿瘤反应和OAR耐受性的背景下进行评估,在这种情况下剂量的任何增加都可以通过增加对正常组织的保护作用来抑制,低分数对正常组织的作用.PACS数量:87.52.-g

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