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Dosimetric comparison of IMRT rectal and anal canal plans generated using an anterior dose avoidance structure

机译:使用前剂量避免结构生成的IMRT直肠和肛管计划的剂量学比较

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To describe a dosimetric method using an anterior dose avoidance structure (ADAS) during the treatment planning process for intensity-modulated radiation therapy (IMRT) for patients with anal canal and rectal carcinomas. A total of 20 patients were planned on the Elekta/CMS XiO treatment planning system, version 4.5.1 (Maryland Heights MO) with a superposition algorithm. For each patient, 2 plans were created: one employing an ADAS (ADAS plan) and the other replanned without an ADAS (non-ADAS plan). The ADAS was defined to occupy the volume between the inguinal nodes and primary target providing a single organ at risk that is completely outside of the target volume. Each plan used the same beam parameters and was analyzed by comparing target coverage, overall plan dose conformity using a conformity number (CN) equation, bowel dose-volume histograms, and the number of segments, daily treatment duration, and global maximum dose. The ADAS and non-ADAS plans were equivalent in target coverage, mean global maximum dose, and sparing of small bowel in low-dose regions (5, 10, 15, and 20. Gy). The mean difference between the CN value for the non-ADAS plans and ADAS plans was 0.04 ± 0.03 (p < 0.001). The mean difference in the number of segments was 15.7 ± 12.7 (p < 0.001) in favor of ADAS plans. The ADAS plan delivery time was shorter by 2.0 ± 1.5 minutes (p < 0.001) than the non-ADAS one. The ADAS has proven to be a powerful tool when planning rectal and anal canal IMRT cases with critical structures partially contained inside the target volume.
机译:描述用于肛门管和直肠癌患者的强度调制放射治疗(IMRT)的治疗计划过程中使用前剂量避免结构(ADAS)的剂量学方法。使用叠加算法,在Elekta / CMS XiO治疗计划系统4.5.1版(Maryland Heights MO)上计划了20位患者。为每位患者创建了2个计划:一个计划采用ADAS(ADAS计划),另一个计划不使用ADAS(非ADAS计划)。 ADAS被定义为占据腹股沟淋巴结和主要目标之间的体积,从而提供一个完全处于目标体积之外的具有风险的单个器官。每个计划都使用相同的波束参数,并通过比较目标覆盖率,使用合格性数(CN)方程式计算的总体计划剂量合格性,肠道剂量-体积直方图以及分段数,每日治疗时间和总体最大剂量进行了分析。 ADAS和非ADAS计划在靶标覆盖范围,平均全球最大剂量以及在低剂量区域(5、10、15和20 Gy)保留小肠的计划相当。非ADAS计划和ADAS计划的CN值之间的平均差为0.04±0.03(p <0.001)。细分数量的平均差异为15.7±12.7(p <0.001),以支持ADAS计划。 ADAS计划的交付时间比非ADAS计划的交付时间缩短了2.0±1.5分钟(p <0.001)。实践证明,ADAS是规划直肠和肛管IMRT病例的关键结构部分包含在目标体积内的强大工具。

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