conformity index

合格指数
  • DOI:
    文章类型: Journal Article
    目的:通过分析基于LINAC的动态适形弧(DCA)技术的立体定向放射外科(SRS)中的剂量分布和生物学效应,评估设置不确定性对最佳剂量范围的综合影响。
    方法:使用四个非共面DCA对Rando头部体模进行CT扫描,共480度弧度,生成SRS治疗计划。将4种不同直径的单个球形计划目标体积(PTV)放置在体模的中心以模拟脑部病变。对于每个PTV,使用相同的剂量计算参数创建5个治疗计划,每个都有5个不同的剂量测定裕度。为了模拟设置不确定性的影响,每个计划的等中心被转移到13个不同的位置。在具有6MV光子束的单个部分中,对49个不同百分比的等剂量表面(%IDS)规定了20Gy的边际剂量。使用符合性指数(CI)评估计划质量,梯度指数(GI),基于EUD的肿瘤控制概率(TCP)正常组织并发症概率(NTCP),和简单的生物目标函数(TCPx(1-NTCP)=p+)。
    结果:与0mm和1mm的剂量测定裕度相比,A+1mm的剂量测定裕度可能会导致更高的p+,而与+2mm和+3mm的剂量测定裕度相比,在一定的%IDS范围内实现等效的p+。具有2mm的设置误差和+1mm的剂量余量,每个PTV优化的%IDS范围为:约80%IDS(10mm直径);63~70%IDS(20mm直径);66~79%IDS(30mm直径)。
    结论:该模拟研究确定了给定设置误差和剂量测定范围的首选处方%IDS,以达到最佳剂量分布和良好的生物学效果。
    OBJECTIVE: To estimate the combined effect of setup uncertainty on optimal dosimetric margin by analyzing the dose distribution and biological effect in LINAC-based stereotactic radiosurgery (SRS) with dynamic conformal arc (DCA) technique.
    METHODS: SRS treatment plans were generated from CT scans of the Rando head phantom using four non-coplanar DCA\'s with total 480-degrees of arc. A single spherical planning target volume (PTV) of 4 different diameters was placed at the center of the phantom to simulate brain lesions. For each PTV, 5 treatment plans were created using identical dose calculation parameters, each with 5 different dosimetric margins. To simulate the effect of setup uncertainty, the isocenter for each plan was shifted to 13 different positions. A marginal dose of 20Gy in a single fraction with 6MV photon beam was prescribed to 49 different percentage isodose surfaces (%IDS). The plan quality was evaluated using Conformity Index (CI), Gradient Index (GI), EUD-based Tumor Control Probability (TCP), Normal Tissue Complication Probability (NTCP), and uncomplicated biological objective function (TCP x (1-NTCP) =p+).
    RESULTS: A +1mm dosimetric margin could result in a much higher p+ compared to 0mm and 1mm dosimetric margins and a smaller GI while achieving an equivalent p+ in a certain range of %IDS compared to +2mm and +3mm dosimetric margins. With 2mm setup error and +1mm dosimetric margin, the %IDS range optimized for each PTV is: around 80%IDS (10mm diameter); 63~70%IDS (20mm diameter); 66~79%IDS (30mm diameter).
    CONCLUSIONS: This simulation study identified the preferred prescription %IDS for a given setup error and dosimetric margin to achieve an optimal dose distribution and favorable biological effect.
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  • 文章类型: Comparative Study
    OBJECTIVE: Our purpose was to explore which immobilization is more suitable for clinical practice in postmastectomy intensity modulation radiotherapy, the single-pole position or the double-pole position?
    METHODS: Patients treated with postmastectomy intensity modulation radiotherapy were eligible. They were selected randomly for single-pole position or double-pole position. Dose-volume histogram (DVH) was used to evaluate plans. After their first radiotherapy, the physicians asked a question about the comfort level of their position. The dosimetric parameters, comfort levels, and reproducibility of the two immobilization techniques were collected and analyzed after all patients had finished the whole radiotherapy.
    RESULTS: Totally, 94 patients were enrolled. Of these, 54 patients were treated with the single-pole position, 28 (51.9%)had left-sided lesions. While 40 patients were treated with the double-pole position, 20 (50%) had left-sided lesions. Patients\' characteristics in two groups were comparable. The single-pole and double-pole immobilizations had similar conformity (0.60 ± 0.05 vs 0.60 ± 0.06, P = 0.887) and homogeneity index (0.14 ± 0.03 vs 0.13 ± 0.03, P = 0.407). Compared to single-pole position, double-pole position typically increased the mean dose, V20 , and V30 of heart (P < 0.05). Moreover, patients in the single-pole group felt more comfortable than another group (P < 0.05). There was no difference in reproducibility between the two groups (P > 0.05).
    CONCLUSIONS: Single-pole position seems to be more comfortable and can reduce dose coverage to heart. Both devices allow for reproducible setup and acceptable dosimetry.
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