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首页> 外文期刊>Biometrical Journal >Critical Assessment of the C-Optimality Design Criteria for Estimating the Median Effective Dose in Quantal Dose-Response Curves
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Critical Assessment of the C-Optimality Design Criteria for Estimating the Median Effective Dose in Quantal Dose-Response Curves

机译:C-最优设计标准的关键评估,用于估计量子剂量-响应曲线的中值有效剂量

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In this paper the properties of C-optimal designs constructed for estimating the median effective dose within the framework of two-parametric linear logistic models are critically assessed. It is well known that this design criterion which is based on the first-order variance approximation of the exact variance of the maximum likelihood estimate of the ED50 leads to a one-point design where the maximum likelihood theory breaks down. The single dose used in this design is identical with the true but unknown value of the ED50. It will be shown, that at this one-point design the asymptotic variance does not exist. A two-point design in the neighbourhood of the one-point design which is symmetrical about the ED50 and associated with a small dose-distance would be nearly optimal, but extremely nonrobust if the best guess of the ED50 differs from the true value. In this situation the asymptotic variance of the two-point design converging towards the one-point design tends to infinity. Moreover, taking in consideration, that for searching an optimal design the exact variance is of primary interest and the asymptotic variance serves only as an approximation of the exact variance, we calculate the exact variance of the estimator from balanced, symmetric 2-point designs in the neighbourhood of the limiting 1-point design for various dose distances and initial best guesses of the ED50. We compare the true variance of the estimate of the ED50 with the asymptotic variance and show that the approximations generally do not represent suitable substitutes for the exact variance even in case of unrealistically large sample sizes. KALISH (1990) proposed a criterion based on the second-order asymptotic variance of the maximum likelihood estimate of the ED50 to overcome the degenerated 1-point design as the solution of the optimization procedure. In fact, we are able to show that this variance approximation does not perform substantially better than the first-order variance. From these considerations it follows, that the C-optimality criterion is not useful in this estimation problem. Other criteria like the F-optimality should be used.
机译:在本文中,对在两参数线性逻辑模型的框架内估算中位数有效剂量的C最优设计的性能进行了严格评估。众所周知,基于ED50的最大似然估计的精确方差的一阶方差近似的这种设计准则导致单点设计,其中最大似然理论失败了。此设计中使用的单剂量与ED50的真实值相同,但未知。将显示,在这种单点设计中,不存在渐近方差。单点设计附近的两点设计相对于ED50对称并且与小剂量距离相关联,这将是最佳选择,但如果ED50的最佳猜测与真实值不同,则该设计将非常不可靠。在这种情况下,两点设计向一点设计收敛的渐近方差趋于无穷大。此外,考虑到为了搜索最优设计,精确方差是主要关注点,而渐近方差仅用作精确方差的近似值,我们根据平衡,对称两点设计计算估计量的精确方差。各种剂量距离和ED50的初始最佳猜测的极限1点设计的邻域。我们将ED50估计值的真实方差与渐近方差进行了比较,结果表明,即使在样本量不切实际的情况下,近似值通常也不能代表精确方差的合适替代品。 KALISH(1990)提出了一个基于ED50最大似然估计的二阶渐近方差的准则,以克服退化的1点设计作为优化程序的解决方案。实际上,我们能够证明这种方差逼近并不能比一阶方差好得多。根据这些考虑,可以得出结论,C最优准则在此估计问题中没有用。应该使用其他标准,例如F最优性。

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