Gaylor D W, Chen J J, Kodell R L
Risk Anal. 1985 Mar;5(1):9-16. doi: 10.1111/j.1539-6924.1985.tb00147.x.
Relatively high doses of chemicals generally are employed in animal bioassays to detect potential carcinogens with relatively small numbers of animals. The problem investigated here is the development of experimental designs which are effective for high to low dose extrapolation for tumor incidence as well as for screening (detecting) carcinogens. Several experimental designs are compared over a wide range of different dose response curves. Linear extrapolation is used below the experimental data range to establish an upper bound on carcinogenic risk at low doses. The goal is to find experimental designs which minimize the upper bound on low dose risk estimates (i.e., maximize the allowable dose for a given level of risk). The maximum tolerated dose (MTD) is employed for screening purposes. Among the designs investigated, experiments with doses at the MTD, 1/2 MTD, 1/4 MTD, and controls generally provide relatively good data for low dose extrapolation with relatively good power for detecting carcinogens. For this design, equal numbers of animals per dose level perform as well as unequal allocations.
在动物生物测定中,通常使用相对高剂量的化学物质,以便用相对较少数量的动物检测潜在致癌物。这里所研究的问题是开发有效的实验设计,这些设计对于从高剂量到低剂量外推肿瘤发生率以及筛查(检测)致癌物都有效。在广泛的不同剂量反应曲线范围内比较了几种实验设计。在实验数据范围以下使用线性外推法来确定低剂量下致癌风险的上限。目标是找到能使低剂量风险估计上限最小化的实验设计(即,对于给定风险水平最大化允许剂量)。最大耐受剂量(MTD)用于筛查目的。在所研究的设计中,使用MTD、1/2 MTD、1/4 MTD剂量以及对照组进行的实验,通常能为低剂量外推提供相对良好的数据,并且具有相对较好的检测致癌物的能力。对于这种设计,每个剂量水平使用相等数量的动物与不相等的分配方式效果相当。