• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

连续给药动物癌症的多阶段预测及其在ED01研究中的应用

Multistage prediction of cancer in serially dosed animals with application to the ED01 study.

作者信息

Brown K G, Hoel D G

出版信息

Fundam Appl Toxicol. 1983 Sep-Oct;3(5):470-7. doi: 10.1016/s0272-0590(83)80022-0.

DOI:10.1016/s0272-0590(83)80022-0
PMID:6642104
Abstract

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)

摘要

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)

相似文献

1
Multistage prediction of cancer in serially dosed animals with application to the ED01 study.连续给药动物癌症的多阶段预测及其在ED01研究中的应用
Fundam Appl Toxicol. 1983 Sep-Oct;3(5):470-7. doi: 10.1016/s0272-0590(83)80022-0.
2
Modeling time-to-tumor data: analysis of the ED01 study.肿瘤发生时间数据建模:ED01研究分析
Fundam Appl Toxicol. 1983 Sep-Oct;3(5):458-69. doi: 10.1016/s0272-0590(83)80021-9.
3
Re-examination of the ED01 study--risk assessment using time.
Fundam Appl Toxicol. 1981 Jan-Feb;1(1):88-123.
4
Two-stage and Weibull models for carcinogenesis applied to the ED01 discontinued dosing data.应用于ED01停药数据的两阶段和威布尔致癌模型。
Environ Health Perspect. 1991 May;92:155-66. doi: 10.1289/ehp.9192155.
5
Re-examination of the ED01 study - adjusting for time on study.对ED01研究的重新审视——根据研究时长进行调整。
Fundam Appl Toxicol. 1981 Jan-Feb;1(1):67-80.
6
Re-examination of the ED01 study. Overview.对ED01研究的重新审视。概述。
Fundam Appl Toxicol. 1981 Jan-Feb;1(1):28-63.
7
Dose and time responses models for the incidence of bladder and liver neoplasms in mice fed 2-acetylaminofluorene continuously.持续喂食2-乙酰氨基芴的小鼠膀胱和肝脏肿瘤发生率的剂量和时间反应模型。
J Environ Pathol Toxicol. 1980;3(3 Spec No):55-68.
8
Re-examination of the ED01 study--technical discussion of the statistical analysis for adjusting for time on study.
Fundam Appl Toxicol. 1981 Jan-Feb;1(1):81-7.
9
Evidence of a "clear and consistent threshold" for bladder and liver cancer in the large ED01 carcinogenicity study.在大型ED01致癌性研究中,存在膀胱癌和肝癌“明确且一致的阈值”的证据。
Toxicol Sci. 2003 Aug;74(2):485; author reply 485-6. doi: 10.1093/toxsci/kfg117. Epub 2003 May 2.
10
Thresholds of carcinogenicity in the ED01 study.ED01研究中的致癌阈值。
Toxicol Sci. 2003 Aug;74(2):486-7; author reply 487-8. doi: 10.1093/toxsci/kfg134.

引用本文的文献

1
Dose-response relationships for carcinogens: a review.致癌物的剂量-反应关系:综述
Environ Health Perspect. 1987 Aug;73:259-306. doi: 10.1289/ehp.8773259.
2
Multistage models for carcinogenesis.癌症发生的多阶段模型。
Environ Health Perspect. 1989 May;81:169-88. doi: 10.1289/ehp.8981169.
3
Two-stage and Weibull models for carcinogenesis applied to the ED01 discontinued dosing data.应用于ED01停药数据的两阶段和威布尔致癌模型。
Environ Health Perspect. 1991 May;92:155-66. doi: 10.1289/ehp.9192155.