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分次立体定向放射治疗中的质量保证

Quality assurance in fractionated stereotactic radiotherapy.

作者信息

Warrington A P, Laing R W, Brada M

机构信息

Physics Department, Royal Marsden Hospital, London, UK.

出版信息

Radiother Oncol. 1994 Mar;30(3):239-46. doi: 10.1016/0167-8140(94)90464-2.

DOI:10.1016/0167-8140(94)90464-2
PMID:8209008
Abstract

The recent development of fractionated stereotactic radiotherapy (SRT), which utilises the relocatable Gill-Thomas-Cosman frame (GTC 'repeat localiser'), requires comprehensive quality assurance (QA). This paper focuses on those QA procedures particularly relevant to fractionated SRT treatments, and which have been derived from the technique used at the Royal Marsden Hospital. They primarily relate to the following: (i) GTC frame fitting, initially in the mould room, and then at each imaging session and treatment fraction; (ii) checking of the linear accelerator beam geometry and alignment lasers; and (iii) setting up of the patient for each fraction of treatment. The precision of the fractionated technique therefore depends on monitoring the GTC frame relocation at each fitting, checking the accuracy of the radiation isocentre of the treatment unit, its coincidence with the patient alignment lasers and the adjustments required to set the patient up accurately. The results of our quality control checks show that setting up to a mean radiation isocentre using precisely set-up alignment lasers can be achievable to within 1 mm accuracy. When this is combined with a mean GTC frame relocatability of 1 mm on the patient, a 2-mm allowance between the prescribed isodose surface and the defined target volume is a realistic safety margin for this technique.

摘要

利用可重新定位的吉尔 - 托马斯 - 科斯曼框架(GTC“重复定位器”)的分次立体定向放射治疗(SRT)的最新发展需要全面的质量保证(QA)。本文重点关注那些与分次SRT治疗特别相关的QA程序,这些程序源自皇家马斯登医院所使用的技术。它们主要涉及以下方面:(i)GTC框架的安装,最初在模具室,然后在每次成像环节和治疗分次时进行;(ii)直线加速器射束几何形状和对准激光的检查;以及(iii)每次治疗分次时患者的摆位。因此,分次技术的精度取决于在每次安装时监测GTC框架的重新定位、检查治疗单元辐射等中心的准确性、其与患者对准激光的重合度以及准确摆位患者所需的调整。我们质量控制检查的结果表明,使用精确设置的对准激光将摆位至平均辐射等中心可实现精度在1毫米以内。当这与患者身上GTC框架平均1毫米的可重新定位性相结合时,规定的等剂量表面与定义的靶体积之间2毫米的余量对于该技术而言是一个现实的安全边际。

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