目的:分析射波刀Synchrony同步追踪系统的质量保证验证方法是否符合临床肿瘤三维运动的要求,以保证射波刀临床治疗的质量.方法:利用改进的Synchrony模体采集CT影像信息,制订同步呼吸追踪的E2E(end to end)治疗验证计划.执行治疗计划,将装有EBT胶片的球方模体放在治疗床上,球方在不同运动条件下执行模拟验证计划,利用E2E软件对照射后的胶片进行分析,得出同步追踪的治疗误差.结果:射波刀Synchrony同步追踪系统在一维、二维、三维方向的治疗误差分别为0.91、1.03、0.90 mm.结论:射波刀Synchrony同步追踪系统的质量保证验证方法满足临床肿瘤精确治疗的要求.%Objective To determine whether the quality insurance verification of Cyberknife Synchrony meet the clinical requirements of 3D tumor motion. Methods CT images were collected with modified Sunchrony phantom, and then a Synchrony E2E treatment plan was developed.A ball-cube with EBT film was loaded on the bed,and then placed in different movement directions to implement phantom verification plan.E2E film analysis software was used for film analysis to obtain the tracking error. Results The treatment accuracy of Synchrony in one-dimensional, two-dimensional and three-dimensional directions were 0.91, 1.03 and 0.90 mm respectively. Conclusion The present quality assurance validation method of Synchrony meets the demand of clinical three-dimensional tumor motion.
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