Hill Thomas, Nelms Mark D, Edwards Stephen W, Martin Matthew, Judson Richard, Corton J Christopher, Wood Charles E
Oak Ridge Institute for Science and Education participant at the National Health and Environmental Effects Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina.
National Health and Environmental Effects Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina.
Toxicol Sci. 2017 Jan;155(1):157-169. doi: 10.1093/toxsci/kfw195. Epub 2016 Sep 27.
Recent international efforts have led to proposals for modified carcinogenicity testing paradigms based on data from shorter-term studies. The main goal of the current study was to evaluate the negative predictive value (NPV) of short-term toxicity indicators on carcinogenicity study outcomes and cancer classifications for chemicals previously reviewed by the U.S. Environmental Protection Agency (EPA). Pathology data were analyzed from over 900 acceptable 2-sex guideline subchronic (3-month) and carcinogenicity studies in the U.S. EPA Toxicity Reference Database. Chemical cancer classifications were obtained from annual reports of the U.S. EPA Office of Pesticide Programs. Histopathologic risk signals and evidence of hormonal perturbation in subchronic rat studies provided 56% NPV for any tumor outcome in the rat or mouse and 75% NPV for cancer classifications not requiring quantitative risk assessment (qRA). In comparison, lack of activity in a battery of 35 in vitro cytotoxicity assays from the U.S. EPA ToxCast library provided 49% NPV for any tumor outcome and 80% NPV for cancer classifications not requiring qRA. These findings support the idea that the absence of short-term bioactivity may provide useful information for prioritizing chemicals based on potential carcinogenic risk. Additional data streams are needed to further refine these models.
近期的国际努力促使人们基于短期研究的数据,提出了修改后的致癌性测试范式建议。本研究的主要目标是评估短期毒性指标对致癌性研究结果和癌症分类的阴性预测值(NPV),这些研究对象是美国环境保护局(EPA)之前审查过的化学物质。从美国EPA毒性参考数据库中分析了900多项可接受的两性指南亚慢性(3个月)和致癌性研究的病理学数据。化学物质的癌症分类来自美国EPA农药项目办公室的年度报告。亚慢性大鼠研究中的组织病理学风险信号和激素干扰证据,对于大鼠或小鼠的任何肿瘤结果,阴性预测值为56%;对于不需要定量风险评估(qRA)的癌症分类,阴性预测值为75%。相比之下,美国EPA ToxCast库中35种体外细胞毒性试验均无活性,对于任何肿瘤结果,阴性预测值为49%;对于不需要qRA的癌症分类,阴性预测值为80%。这些发现支持了这样一种观点,即缺乏短期生物活性可能为基于潜在致癌风险对化学物质进行优先级排序提供有用信息。需要更多的数据流来进一步完善这些模型。