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Evaluation of a combined respiratory‐gating system comprising the TrueBeam linear accelerator and a new real‐time tumor‐tracking radiotherapy system: a preliminary study

机译:评估包括TrueBeam线性加速器和新型实时肿瘤跟踪放疗系统的组合呼吸门控系统:一项初步研究

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A combined system comprising the TrueBeam linear accelerator and a new real-time, tumor-tracking radiotherapy system, SyncTraX, was installed in our institution. The goals of this study were to assess the capability of SyncTraX in measuring the position of a fiducial marker using color fluoroscopic images, and to evaluate the dosimetric and geometric accuracy of respiratory-gated radiotherapy using this combined system for the simple geometry. For the fundamental evaluation of respiratory-gated radiotherapy using SyncTraX, the following were performed: 1) determination of dosimetric and positional characteristics of sinusoidal patterns using a motor-driven base for several gating windows; 2) measurement of time delay using an oscilloscope; 3) positional verification of sinusoidal patterns and the pattern in the case of a lung cancer patient; 4) measurement of the half-value layer (HVL in mm AL), effective kVp, and air kerma, using a solid-state detector for each fluoroscopic condition, to determine the patient dose. The dose profile in a moving phantom with gated radiotherapy having a gating window ≤ 4 mm was in good agreement with that under static conditions for each photon beam. The total time delay between TrueBeam and SyncTraX was 227 ms for each photon beam. The mean of the positional tracking error was 0.4 mm for sinusoidal patterns and for the pattern in the case of a lung cancer patient. The air-kerma rates from one fluoroscopy direction were 1.93 ± 0.01 , 2.86 ± 0.01 , 3.92 ± 0.04 , 5.28 ± 0.03 , and 6.60 ± 0.05 mGy / min for 70, 80, 90, 100, and 110 kV X-ray beams at 80 mA, respectively. The combined system comprising TrueBeam and SyncTraX could track the motion of the fiducial marker and control radiation delivery with reasonable accuracy; therefore, this system provides significant dosimetric improvement. However, patient exposure dose from fluoroscopy was not clinically negligible.PACS number(s): 87.53.Bn, 87.55.km, 87.55.Qr
机译:我们机构安装了由TrueBeam线性加速器和新的实时肿瘤跟踪放射治疗系统SyncTraX组成的组合系统。这项研究的目的是评估使用彩色荧光透视图像测量SyncTraX在基准标记位置中的功能,并使用此组合系统评估简单几何结构的呼吸门控放射疗法的剂量和几何精度。为了对使用SyncTraX进行的呼吸门放射治疗进行基本评估,进行了以下操作:1)使用几个门窗的电机驱动底座确定正弦波模式的剂量和位置特征; 2)使用示波器测量时间延迟; 3)正弦波模式的位置验证以及肺癌患者的模式; 4)使用每种荧光检查条件的固态检测器,测量半值层(HVL,单位为mm AL),有效kVp和空气比释动能,以确定患者剂量。门控窗≤4 mm的带门放射疗法的移动体模中的剂量分布与静态条件下每个光子束的剂量分布非常吻合。每个光子束在TrueBeam和SyncTraX之间的总时间延迟为227 ms。对于正弦波模式和对于肺癌患者,该模式的位置跟踪误差的平均值为0.4 mm。对于70 kV,80 kV,90 kV,100 kV和110 kV X射线束,在一个透视方向上的空气比释动能速率分别为1.93±0.01、2.86±0.01、3.92±0.04、5.28±0.03和6.60±0.05 mGy / min分别为80 mA。由TrueBeam和SyncTraX组成的组合系统可以跟踪基准标记的运动,并以合理的精度控制辐射的传输;因此,该系统显着改善了剂量学。然而,透视检查的患者暴露剂量在临床上不能忽略不计.PACS编号:87.53.Bn,87.55.km,87.55.Qr

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