[实验性致癌性评价研究]。

R Maximilien, M Morin
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引用次数: 0

摘要

在许多情况下,流行病学研究证明了职业接触和工业过程的致癌风险,但不允许评估接触中涉及的各种物质的致癌潜力(物种形成)。纯物质的分类和标签需要结合人类和动物数据的专家判断。为了辅助决策,建立了一种批判性的实验性癌变评价方法:1。根据纯物质、种类、菌株和给药途径建立标准化毒理学档案。2. 方法学评估采用基于3个关键参数的方案进行:研究时间应延长至研究物种的预期寿命;样本量,根据样本量确定阴性实验的统计显著性;群体的存活率,因为足够数量的动物在其生命的大部分时间里应该处于危险之中。3.对风险评估结果进行分类,考虑到给药途径的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Evaluation studies of experimental carcinogenesis].

In many cases, epidemiological studies demonstrate carcinogenic risk of occupational exposures and industrial processes, but do not allow to assess carcinogenic potential of the various substances involved in exposures (speciation). Expert judgment combining human and animal data is needed for classifying and labelling of the pure substances. For decision aiding purpose, a method was established for reviewing critically experimental carcinogenesis: 1. Standardized toxicological profiles are established according to pure substances, species, strains and administration routes. 2. Methodological evaluation is made using a scheme based on 3 critical parameters: study duration which should extend to the life expectancy of the species under study; sample size, the statistical significance of negative experiments being ascertained depending on size of samples; survival rates of groups, since sufficient numbers of animals should be at risk during most of their life span. 3. Classification of the results for risk assessment, taking into account the relevance of the administration routes.

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