Brown K G, Hoel D G
Fundam Appl Toxicol. 1983 Sep-Oct;3(5):470-7. doi: 10.1016/s0272-0590(83)80022-0.
The ED01 study is a large-scale experiment in which mice were exposed to the known carcinogen 2-acetylaminofluorene (2-AAF). The dosing was continuous until time of death for most of the mice. However, for some mice, dosing was terminated at specified intervals prior to sacrifice time. Exploratory model fitting of the continuous dosing data of sacrificed mice using liver neoplasms as the endpoint was conducted by Brown and Hoel (1982). They report that the multistage model of Armitage and Doll (1954) fits the data moderately well, however a much improved fit with fewer parameters is attainable by a modified multistage model. These two models, with parameter estimates obtained from the data on continuous dosing, are referred to in this paper as Model 1 and Model 2, respectively. Models 1 and 2 are extended to provide for termination of dosing prior to time of sacrifice. The resultant equations are used to predict cancer responses in the serial dosing part of the ED01 study, and then are compared to the actual observed tumor frequencies. The objective is to evaluate the change in cancer risk over time after dosing is terminated, and to establish which stages in the multistage process are affected by dose. The predictive capabilities of the two models are compared and contrasted. Model 1, which presumes four stages of which two are affected by dose, predicts only moderately well and is inconclusive as to which two of the stages are the ones affected. Model 2, which differs from the multistage model by using a "J-shaped" curve instead of a polynomial for the dose metameter, provides an improvement over Model 1.(ABSTRACT TRUNCATED AT 250 WORDS)
ED01研究是一项大规模实验,其中小鼠被暴露于已知致癌物2-乙酰氨基芴(2-AAF)。对于大多数小鼠,给药持续至死亡。然而,对于一些小鼠,在处死前的特定间隔终止给药。Brown和Hoel(1982年)使用肝肿瘤作为终点对处死小鼠的连续给药数据进行了探索性模型拟合。他们报告说,Armitage和Doll(1954年)的多阶段模型对数据拟合得还算不错,然而,通过改进的多阶段模型可以用更少的参数获得更好的拟合。从连续给药数据中获得参数估计值的这两个模型,在本文中分别称为模型1和模型2。模型1和模型2进行了扩展,以考虑在处死前终止给药的情况。所得方程用于预测ED01研究连续给药部分的癌症反应,然后与实际观察到的肿瘤频率进行比较。目的是评估给药终止后癌症风险随时间的变化,并确定多阶段过程中的哪些阶段受剂量影响。对这两个模型的预测能力进行了比较和对比。模型1假定有四个阶段,其中两个受剂量影响,其预测效果一般,并且关于受影响的是哪两个阶段尚无定论。模型2与多阶段模型的不同之处在于,它使用“J形”曲线而不是多项式来表示剂量参数,比模型1有所改进。(摘要截取自250个单词)