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Statistical methods to evaluate the correlation between measured and calculated dose using quality assurance method in IMRT

机译:在IMRT中使用质量保证方法评估测量和计算剂量之间的相关性的统计学方法

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摘要

Purpose: the objective of this study is to validate a procedure based on a statistical method to assess the agreement and the correlation between measured and calculated dose in the process of quality assurance (QA) for Intensity-Modulated Radiation Therapy (IMRT).Patients and methods: 10 patients including 56 fields for head and neck cancer treatment were analyzed. For each patient, one treatment plan was generated using Eclipse TPS®. To compare the calculated dose with measured dose a CT-scan of solid water slabs (30 × 30 × 15 cm3) was used. The measurements were done for absolute dose by a pinpoint ionization chamber and 2D dose distributions using electronic portal imaging device dosimetry. Six criteria levels were applied for each case (3%, 3 mm), (4%, 3 mm), (5%, 3 mm), (4%, 4 mm), (5%, 4 mm) and (5%, 5 mm). The normality of the data and the variance homogeneity were tested using Shapiro-Wilks test and Levene’s test, respectively. Wilcoxon signed-rank paired test was used to calculate p-value. Bland-Altman method was used to calculate the limit of agreement between calculated and measured doses and to draw a scatter plot. The correlation between calculated and measured doses was assessed using Spearman’s rank test.Results: The statistical tests indicate that the data do not fulfill normal distribution, p < 0.001 and had a homogenous variance, p = 0.85. The upper and lower limit of agreements for absolute dose measurements were 6.44% and -6.40%, respectively. Wilcoxon test indicated a significance difference between calculated and measured dose with ionization chamber, p = 0.01. Spearman’s test indicated a strong correlation between calculated and absolute measured dose, ρ = 0.99. Therefore, there is a lack of correlation between dose difference for absolute dose measurements and gamma passing rates for 2D dose measurements.Conclusion: the statistical tests showed that the common acceptance criteria’s using gamma evaluation are not able to predict the dose difference for a global treatment plan or per beam. The current QA method is limited to protect the patient. The described method provides an overall analysis for dosimetric data issued from calculation and measurement and it can be quickly integrated in QA system for IMRT.
机译:目的:目的本研究的是验证基于统计的方法来评估中协议和质量保证(QA)的过程为调强放射疗法(IMRT)。患者和测量和计算剂量之间的相关性的程序方法:10名患者包括头部和颈部癌症治疗领域56进行分析。对于每位患者,使用EclipseTPS®产生一个治疗计划。以比较剂量CT扫描,使用固体水板坯(30×30×15厘米3)的测量的计算的剂量。测量通过针尖电离室对绝对剂量完成和2D使用电子射野成像装置剂量测定剂量分布。六个标准水平应用于每一种情况下(3%,3 mm)时,(4%,3 mm)时,(5%,3 mm)时,(4%,4 mm)时,(5%,4毫米),(5 %,5毫米)。所述数据和所述方差均匀性的正常使用所测试夏皮罗 - 威尔克斯测试和列文的测试,分别。 Wilcoxon符号秩配对检验用于计算p值。奥特曼使用的方法来计算计算的和测量的剂量之间的协议的限制和绘制的散点图。计算和测量的剂量之间的相关性使用Spearman秩检验。结果评定:统计测试表明,该数据不符合正态分布,P <0.001,有一个均匀的方差,p值= 0.85。绝对剂量测量协定的上限和下限分别是6.44%和-6.40%。 Wilcoxon检验表明与电离室,p值= 0.01计算的和测量的剂量之间的显着性差异。斯皮尔曼试验表明计算的和绝对的测量剂量之间的强相关性,ρ= 0.99。因此,一个缺乏绝对剂量测量和2D剂量measurements.Conclusion伽马合格率剂量差之间的相关性:显示了统计检验的普遍接受标准的使用伽玛评价不能预测剂量差异为全球治疗计划或每束。目前的QA方法仅限于保护患者。所描述的方法提供了用于从计算和测量发出剂量测定数据的全面分析,它可以迅速地集成在QA系统IMRT。

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