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首页> 外文期刊>Technology in cancer research & treatment. >Converting Treatment Plans From Helical Tomotherapy to L-Shape Linac: Clinical Workflow and Dosimetric Evaluation
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Converting Treatment Plans From Helical Tomotherapy to L-Shape Linac: Clinical Workflow and Dosimetric Evaluation

机译:将治疗计划从螺旋断层疗法转变为L型直线加速器:临床工作流程和剂量学评估

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This work evaluated a commercial fallback planning workflow designed to provide cross-platform treatment planning and delivery. A total of 27 helical tomotherapy intensity-modulated radiotherapy plans covering 4 anatomical sites were selected, including 7 brain, 5 unilateral head and neck, 5 bilateral head and neck, 5 pelvis, and 5 prostate cases. All helical tomotherapy plans were converted to 7-field/9-field intensity-modulated radiotherapy and volumetric-modulated radiotherapy plans through fallback dose-mimicking algorithm using a 6-MV beam model. The planning target volume (PTV) coverage (D1, D99, and homogeneity index) and organs at risk dose constraints were evaluated and compared. Overall, all 3 techniques resulted in relatively inferior target dose coverage compared to helical tomotherapy plans, with higher homogeneity index and maximum dose. The organs at risk dose ratio of fallback to helical tomotherapy plans covered a wide spectrum, from 0.87 to 1.11 on average for all sites, with fallback plans being superior for brain, pelvis, and prostate sites. The quality of fallback plans depends on the delivery technique, field numbers, and angles, as well as user selection of structures for organs at risk. In actual clinical scenario, fallback plans would typically be needed for 1 to 5 fractions of a treatment course in the event of machine breakdown. Our results suggested that <1% dose variance can be introduced in target coverage and/or organs at risk from fallback plans. The presented clinical workflow showed that the fallback plan generation typically takes 10 to 20 minutes per case. Fallback planning provides an expeditious and effective strategy for transferring patients cross platforms, and minimizing the untold risk of a patient missing treatment(s).
机译:这项工作评估了商业后备计划工作流,该工作流旨在提供跨平台的治疗计划和交付。总共选择了27个螺旋层析疗法强度调制放射疗法,覆盖了4个解剖部位,包括7个脑,5个单侧头和颈,5个双侧头和颈,5个骨盆和5个前列腺病例。通过使用6-MV射线模型的后备剂量模拟算法,将所有螺旋断层扫描计划转换为7场/ 9场强度调制放射治疗和体积调制放射治疗计划。评估并比较了计划目标体积(PTV)覆盖范围(D 1 ,D 99 和同质性指标)和受风险剂量约束的器官。总体而言,与螺旋层析疗法相比,所有这三种技术均导致目标剂量覆盖率相对较低,且均一性指数和最大剂量更高。后备与螺旋断层放疗计划的风险剂量比范围广泛,所有部位平均在0.87至1.11之间,而后备计划在脑部,骨盆和前列腺部位的表现更好。后备计划的质量取决于投放技术,场数和角度,以及用户对有风险器官的结构选择。在实际的临床情况中,如果机器发生故障,通常需要针对一到五分之一疗程的后备计划。我们的结果表明,可以将<1%的剂量差异引入目标覆盖范围和/或具有后备计划风险的器官。所呈现的临床工作流程表明,生成后备计划通常每个案例需要10到20分钟。后备计划提供了一种快速有效的策略,可以跨平台转移患者,并最大程度地降低患者错过治疗的巨大风险。

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