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Treatment planning comparison of volumetric modulated arc therapy employing a dual-layer stacked multi-leaf collimator and helical tomotherapy for cervix uteri

机译:体积调制电弧疗法的处理比较采用双层堆叠多叶准直器和颈椎螺旋疗法

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To ascertain the dosimetric performance of a new delivery system (the Halcyon system, H) equipped with dual-layer stacked multi-leaf collimator (MLC) for risk-adapted targets in cervix uteri cancer patients compared to another ring-based system in clinical operation (Helical Tomotherapy, HT). Twenty patients were retrospectively included in a treatment planning study (10 with positive lymph nodes and 10 without). The dose prescription (45Gy to the primary tumour volume and a simultaneously integrated boost up to 55Gy for the positive patients) and the clinical planning objectives were defined consistently as recommended by an ongoing multicentric clinical trial. Halcyon plans were optimised for the volumetric modulated arc therapy. The plan comparison was performed employing the quantitative analysis of the dose-volume histograms. The coverage of the primary and nodal target volumes was comparable for both techniques and both subsets of patients. The primary planning target volume (PTV) receiving at least 95% of the prescription isodose ranged from 97.2?±?1.1% (node-negative) to 99.1?±?1.2% (node-positive) for H and from 96.5?±?1.9% (node-negative) to 98.3?±?0.9% (node-positive) for HT. The uncertainty is expressed at one standard deviation from the cohort of patient per each group. For the nodal clinical target volumes, the dose received by 98% of the planning target volume ranged 55.5?±?0.1 to 56.0?±?0.8Gy for H and HT, respectively. The only significant and potentially relevant differences were observed for the bowels. In this case, V40Gy resulted 226.3?±?35.9 and 186.9?±?115.9?cm3 for the node-positive and node-negative patients respectively for Halcyon. The corresponding findings for HT were: 258.9?±?60.5 and 224.9?±?102.2?cm3. On the contrary, V15Gy resulted 1279.7?±?296.5 and 1557.2?±?359.9?cm3 for HT and H respectively for node-positive and 1010.8?±?320.9 versus 1203.8?±?332.8?cm3 for node-negative. This retrospective treatment planning study, based on the dose constraints derived from the Embrace II study protocol, suggested the essential equivalence between Halcyon based and Helical Tomotherapy based plans for the intensity-modulated rotational treatment of cervix uteri cancer. Different levels of sparing were observed for the bowels with H better protecting in the high-dose region and HT in the mid-low dose regions. The clinical impact of these differences should be further addressed.
机译:为了确定具有双层堆叠多叶准直器(MLC)的新递送系统(Halcyon System,H)的剂量性能,用于宫颈子宫癌症患者的风险适应的靶标,与临床操作中的另一个环形系统相比(螺旋疗法,HT)。批评了20名患者在治疗计划研究中(10个阳性淋巴结和10个没有)。剂量处方(45Gy到主要肿瘤体积和阳性患者的同时集成的增压)和临床规划目标是持续的多中心临床试验的推荐定义。为体积调制的电弧疗法进行了优化了Halcyon计划。进行计划比较采用剂量 - 体积直方图的定量分析。初级和节点靶体积的覆盖率对于患者的技术和既有亚群相当。接受至少95%的处方体体积(PTV)的主要规划目标体积(PTV)从97.2?±1.1%(节点阴性)到99.1?±1.2%(Node阳性)(Node-阳性),从96.5?±? 1.9%(节点阴性)至98.3?±0.9%(Node阳性)的HT。不确定性在每个组的患者队列的一个标准偏差中表达。对于节点临床目标体积,98%的规划目标体积接收的剂量范围为55.5?±0.1至56.0?±0.8gs,分别为H和HT。对肠道唯一的显着和潜在的相关差异。在这种情况下,V40Gy产生226.3?±35.9和186.9?±115.9℃,分别为卤代节点阳性和节点阴性患者。 HT的相应发现是:258.9?±60.5和224.9?±102.2?cm3。相反,v15gy导致1279.7?±296.5和1557.2?±359.9?cm 3分别用于节点阳性和1010.8±320.8与1203.8与1203.8?332.8?332.8?332.8?332.8?CM3用于节点负数。该回顾性治疗计划研究基于来自II族研究方案的剂量约束,表明了基于赤胞基和螺旋旋转治疗的基于卤代和螺旋疗法的基本性等效性。对于在高剂量区域和中低剂量区域中的高剂量区域更好地保护肠道,观察到不同水平的备注。应进一步解决这些差异的临床影响。

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