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Verification and dosimetric impact of Acuros XB algorithm on intensity modulated stereotactic radiotherapy for locally persistent nasopharyngeal carcinoma

机译:Acuros XB算法对调强立体定向放射治疗局部持续性鼻咽癌的验证及剂量学影响

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Purpose: The main aim of the current study was to assess the dosimetric impact on intensity modulated stereotactic radiotherapy (IMSRT) for locally persistent nasopharyngeal carcinoma (NPC) due to the recalculation from the Anisotropic Analytical Algorithm (AAA) to the recently released Acuros XB (AXB) algorithm. The dosimetric accuracy of using AXB in predicting airtissue interface doses from an open single small field in a simple geometric phantom and intensity modulated small fields in an anthropomorphic phantom was also investigated. Methods: The central axis percentage depth doses (PDD) of a rectangular phantom containing an air cavity were calculated by both AAA and AXB from 6 MV beam with small field sizes (2 × 2 to 5 × 5 cm 2). These data were compared to PDD measured by thin thermoluminescent dosimeters (TLDs) and Monte Carlo simulations. The doses predicted by AAA and AXB near airtissue interfaces from five different IMSRT plans were compared to the TLD measured doses in an anthropomorphic phantom. The PTV coverage, conformity and doses to organs at risk (OARs) calculated by AAA and AXB were compared for 12 patients, using identical beam setup, leaves movement and monitor units. Results: Testing using the simple rectangular phantom demonstrated that AAA and AXB overestimated the PDD at the airtissue interfaces by up to 41 and 6, respectively, from a 2 × 2 cm 2 field. The secondary build-up curves predicted by AXB caught up well with the measured data at around 2 mm beyond the air cavity. Testing using the anthropomorphic phantom showed that AAA overestimated the doses by up to 10, while the measured doses matched those of the AXB to within 3. Using AAA, the planning target coverage represented by 100 of the reference dose was estimated to be 4 higher than using AXB. The averaged minimum dose to the PTV predicted by AAA was about 4 higher and OARs doses 3 to 6 higher compared to AXB. Conclusions: AXB should be used whenever possible as the standard reference for IMSRT boost of NPC cases. The more accurate AXB indicating lower target coverage and lower minimum target dose compared to AAA should be noted.
机译:目的:本研究的主要目的是评估由于各向异性分析算法(AAA)重新计算为最近发布的Acuros XB(局部重度鼻咽癌(NPC)而对剂量调制立体定向放射疗法(IMSRT)的剂量学影响) AXB)算法。还研究了使用AXB从简单的几何体模中的开放单个小视野和拟人体模中的强度调制小视野预测空气组织界面剂量的剂量学准确性。方法:采用AAA和AXB两种方法,从6 MV小视场束(2×2至5×5 cm 2)中计算出包含空气腔的矩形幻影的中心轴百分比深度剂量(PDD)。将这些数据与通过薄热发光剂量计(TLD)和蒙特卡洛模拟测量的PDD进行比较。将AAA和AXB预测的来自五个不同IMSRT计划的接近气管界面的剂量与拟人化体模中TLD测得的剂量进行了比较。使用相同的光束设置,叶片运动和监控单元,比较了AAA和AXB计算的PTV覆盖范围,符合性和由AAA和AXB计算的高危器官剂量(OAR)。结果:使用简单的矩形体模进行的测试表明,在2×2 cm 2的视野中,AAA和AXB高估了空气组织界面的PDD分别高达41和6。 AXB预测的二次堆积曲线在距气腔约2 mm处与测量数据相吻合。使用拟人化体模进行的测试表明,AAA高估了剂量达10倍,而测得的剂量与AXB的剂量相差不超过3倍。使用AAA,用100倍的参考剂量表示的计划目标覆盖率估计要高出4倍。使用AXB。由AAA预测,PTV的平均最小剂量比AXB高约4倍,OAR剂量高3至6倍。结论:应尽可能将AXB用作NPC病例的IMSRT增强的标准参考。应当指出,与AAA相比,更准确的AXB表示更低的目标覆盖率和更低的最小目标剂量。

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