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立体定向同步加速器放射治疗临床试验中剂量递增的生物等效剂量研究。

Biological equivalent dose studies for dose escalation in the stereotactic synchrotron radiation therapy clinical trials.

作者信息

Prezado Y, Fois G, Edouard M, Nemoz C, Renier M, Requardt H, Estève F, Adam J F, Elleaume H, Bravin A

机构信息

ID17 Biomedical Beamline, European Synchrotron Radiation Facility (ESRF), 6 rue Jules Horowitz, BP 220, 38043 Grenoble Cedex, France.

出版信息

Med Phys. 2009 Mar;36(3):725-33. doi: 10.1118/1.3070538.

Abstract

Synchrotron radiation is an innovative tool for the treatment of brain tumors. In the stereotactic synchrotron radiation therapy (SSRT) technique a radiation dose enhancement specific to the tumor is obtained. The tumor is loaded with a high atomic number (Z) element and it is irradiated in stereotactic conditions from several entrance angles. The aim of this work was to assess dosimetric properties of the SSRT for preparing clinical trials at the European Synchrotron Radiation Facility (ESRF). To estimate the possible risks, the doses received by the tumor and healthy tissues in the future clinical conditions have been calculated by using Monte Carlo simulations (PENELOPE code). The dose enhancement factors have been determined for different iodine concentrations in the tumor, several tumor positions, tumor sizes, and different beam sizes. A scheme for the dose escalation in the various phases of the clinical trials has been proposed. The biological equivalent doses and the normalized total doses received by the skull have been calculated in order to assure that the tolerance values are not reached.

摘要

同步辐射是一种用于治疗脑肿瘤的创新工具。在立体定向同步辐射治疗(SSRT)技术中,可实现针对肿瘤的辐射剂量增强。肿瘤被注入高原子序数(Z)元素,并在立体定向条件下从多个入射角进行照射。这项工作的目的是评估SSRT的剂量学特性,以便在欧洲同步辐射装置(ESRF)开展临床试验。为了估计可能的风险,通过蒙特卡罗模拟(PENELOPE代码)计算了未来临床条件下肿瘤和健康组织所接受的剂量。已针对肿瘤中不同的碘浓度、多种肿瘤位置、肿瘤大小以及不同的射束尺寸确定了剂量增强因子。已提出了临床试验各阶段的剂量递增方案。计算了颅骨所接受的生物等效剂量和归一化总剂量,以确保不超过耐受值。

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