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Development of a Clinical Prototype for Range Verification in Proton Therapy based on Prompt Gamma-Ray Spectroscopy

机译:基于促进γ射线光谱法的质子疗法临床原型的开发

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Range uncertainties in proton therapy pose a limitation on its benefits for cancer treatment. Robust planning and conservative safety margins of up to 1 cm are necessary for guaranteeing full tumor coverage, at the price of a larger dose to normal tissue. At the Massachusetts General Hospital, a full-scale prototype system for in vivo proton range verification is under development, based on spectroscopy of prompt gamma-rays emitted from proton-nuclear reactions with tissue. The aim is to verify the proton range during patient treatments with 1 mm precision. The system consists of eight LaBr3 detectors and a tungsten collimator that are mounted on a rotating frame. The electronics and data processing algorithms are designed to cope with the highly variable count rates that occur during pencil-beam scanning. The prototype was tested by irradiating a water phantom with a clinical dose of 0.9 Gy, a beam current of 2 nA and a field size of 10 cm x 10 cm. Energy- and time-resolved gamma-ray spectra were acquired during the irradiation and further analyzed to subtract the neutron background and to determine the prompt gamma-ray line magnitudes. A GPU-accelerated Monte Carlo model of the gamma-ray emissions was developed, which relies on measured nuclear reaction cross sections and the treatment plan CT. We reconstruct both the absolute proton range and the elemental concentrations of the irradiated tissue by minimizing the deviation between the measurement and the parameterized model. Range shifters and changes in the elemental composition were introduced in different parts of the water phantom to verify the precision and robustness of the range verification method. A statistical precision of 1.1 mm at 95% confidence level and a mean systematic error of 0.5 mm were obtained, when merging protons delivered to the two distal pencil-beam layers within a 10 mm radius. In an upcoming clinical study, the prototype will be tested during the treatment of brain cancer patients.
机译:质子疗法中的范围不确定性对癌症治疗的益处提出了限制。在较大剂量到正常组织的价格下,稳健规划和保守的安全边缘最多可达1厘米。在马萨诸塞州综合医院,基于从质子核反应与组织的质子核反应排出的迅速伽马射线的光谱,正在开发中为体内质子范围验证的全面原型系统。目的是在患者治疗期间验证质子范围,精度为1毫米。该系统由八个Labr3探测器和安装在旋转框架上的钨准直器组成。电子和数据处理算法旨在应对铅笔束扫描期间发生的高度变计数。通过用0.9GY的临床剂量照射水体模,2NA的光束电流和10cm×10cm的场尺寸来测试原型。在照射期间获得能量和时间分辨的γ射线光谱,进一步分析以减去中子背景并确定提示伽马射线幅度。开发了一种GPU加速的伽马射线排放的蒙特卡罗模型,依赖于测量的核反应横截面和治疗计划CT。通过最小化测量和参数化模型之间的偏差,我们重建绝对质子范围和辐照组织的元素浓度。在水模型的不同部分引入了频率转换器和元素组合物的变化,以验证范围验证方法的精度和稳健性。当将递送到10mm半径内的两个远端铅笔束层的质子合并时,获得统计精度为95%的置信水平和0.5mm的平均系统误差。在即将到来的临床研究中,原型将在治疗脑癌患者期间进行测试。

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