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用于致癌物筛查的一些实验设计的比较与评估。

Comparison and evaluation of some experimental designs for use in carcinogen screening.

作者信息

Elashoff R M, Preston D L, Fears T R

出版信息

J Natl Cancer Inst. 1979 May;62(5):1209-19.

PMID:286098
Abstract

The development and evaluation of experimental designs for routine in vivo screening of chemicals for potential carcinogenic activity were considered. Such designs have played an important role in the Carcinogenesis Bloassay Program of the National Cancer Institute (NCI). In particular, the current one-stage 50-animal/group screen used by the NCI was considered. A specific two-stage alternative was proposed in which 35 animals/group were used; this alternative allowed for retesting of equivocal compounds. The proposed designs were evaluated in terms of sensitivity, specificity, and throughout. Despite the large number of tests made for each compound, the false-positive rate was found to be less than 0.07 for the current screen and less than 0.05 for the proposed two-stage alternative. The power of the one-stage and two-stage screens was comparable. The two-stage screen was shown to make about 30% more decisions per test period with a savings of around 28% in the expected number of animals needed per compound tested.

摘要

对用于化学品潜在致癌活性常规体内筛选的实验设计的开发与评估进行了考量。此类设计在国立癌症研究所(NCI)的致癌性生物测定项目中发挥了重要作用。特别地,对NCI目前使用的每组50只动物的单阶段筛选进行了考量。提出了一种特定的两阶段替代方案,其中每组使用35只动物;该替代方案允许对可疑化合物进行重新测试。从敏感性、特异性和通量方面对所提出的设计进行了评估。尽管对每种化合物进行了大量测试,但发现当前筛选的假阳性率低于0.07,而所提出的两阶段替代方案的假阳性率低于0.05。单阶段和两阶段筛选的效能相当。结果表明,两阶段筛选在每个测试周期内做出的决策数量大约多30%,同时在每种测试化合物所需的预期动物数量方面节省约28%。

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