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Estimation of parameters of dose-volume models and their confidence limits

机译:剂量-体积模型的参数估计及其置信度

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Predictions of the normal-tissue complication probability (NTCP) for the ranking of treatment plans are based on fits of dose-volume models to clinical and/or experimental data. In the literature several different fit methods are used. In this work frequently used methods and techniques to fit NTCP models to dose response data for establishing dose-volume effects, are discussed. The techniques are tested for their usability with dose-volume data and NTCP models. Different methods to estimate the confidence intervals of the model parameters are part of this study. From a critical-volume (CV) model with biologically realistic parameters a primary dataset was generated, serving as the reference for this study and describable by the NTCP model. The CV model was fitted to this dataset. From the resulting parameters and the CV model, 1000 secondary datasets were generated by Monte Carlo simulation. All secondary datasets were fitted to obtain 1000 parameter sets of the CV model. Thus the 'real' spread in fit results due to statistical spreading in the data is obtained and has been compared with estimates of the confidence intervals obtained by different methods applied to the primary dataset. The confidence limits of the parameters of one dataset were estimated using the methods, employing the covariance matrix, the jackknife method and directly from the likelihood landscape. These results were compared with the spread of the parameters, obtained from the secondary parameter sets. For the estimation of confidence intervals on NTCP predictions, three methods were tested. Firstly, propagation of errors using the covariance matrix was used. Secondary, the meaning of the width of a bundle of curves that resulted from parameters that were within the one standard deviation region in the likelihood space was investigated. Thirdly, many parameter sets and their likelihood were used to create a likelihood-weighted probability distribution of the NTCP. It is concluded that for the type of dose response data used here, only a full likelihood analysis will produce reliable results. The often-used approximations, such as the usage of the covariance matrix, produce inconsistent confidence limits on both the parameter sets and the resulting NTCP values.
机译:对治疗计划进行排名的正常组织并发症概率(NTCP)的预测是基于剂量-体积模型对临床和/或实验数据的拟合。在文献中使用了几种不同的拟合方法。在这项工作中,讨论了将NTCP模型拟合到剂量响应数据以建立剂量-体积效应的常用方法和技术。使用剂量数据和NTCP模型测试了这些技术的可用性。估计模型参数置信区间的不同方法是本研究的一部分。从具有生物学实际参数的临界体积(CV)模型中,生成了一个主要数据集,可作为本研究的参考并由NTCP模型描述。 CV模型适合此数据集。根据所得参数和CV模型,通过蒙特卡洛模拟生成了1000个辅助数据集。拟合所有次要数据集以获得1000个CV模型参数集。因此,获得了由于数据中的统计分布而导致的拟合结果的“真实”分布,并将其与通过应用于主要数据集的不同方法获得的置信区间的估计值进行了比较。使用协方差矩阵,折刀法和直接从似然态势中估算出一个数据集参数的置信极限。将这些结果与从次级参数集获得的参数分布进行了比较。为了估计NTCP预测的置信区间,测试了三种方法。首先,使用协方差矩阵传播误差。其次,研究了由似然空间中一个标准偏差区域内的参数导致的曲线束宽度的含义。第三,许多参数集及其似然性用于创建NTCP的似然加权概率分布。结论是,对于此处使用的剂量响应数据类型,只有完全似然分析才能产生可​​靠的结果。经常使用的近似值(例如协方差矩阵的使用)会在参数集和所得的NTCP值上产生不一致的置信度限制。

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