EPA修订的癌症评估指南的实施:结合机制和药代动力学数据

N.P. Page , D.V. Singh , W. Farland , J.I. Goodman , R.B. Conolly , M.E. Andersen , H.J. Clewell , C.B. Frederick , H. Yamasaki , G. Lucier
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引用次数: 20

摘要

1996年在加利福尼亚州阿纳海姆举行的第35届毒理学学会年会上,举行了题为“实施EPA修订的癌症评估指南:结合机制和药代动力学数据”的讲习班。本次研讨会由SOT的致癌、风险评估和兽医专业部门联合主办。讲习班的主旨是讨论修订环境保护署癌症评估准则的科学依据以及环境保护署实施这些准则的计划。这是对EPA自1986年以来一直使用的原始EPA指南的第一次修订。主要修订的目的是提供一个框架,以便提高将生物数据纳入风险评估过程的能力。提出了关于氯仿和三氯乙烯的两个案例,证明了将修订后的准则用于特定癌症风险评估。使用这些新指南,对这些化学物质提出了非线性暴露裕度分析,而不是EPA先前使用的线性多阶段模型作为默认方法。研讨会的与会者普遍对EPA指导方针的修订计划表示欢迎。在大多数情况下,他们认为修订后的准则是一个积极的步骤,应该允许和鼓励在进行癌症风险评估时使用生物资料。然而,一些与会者告诫说,癌症风险评估的主要问题仍然是现有数据不足,无法进行更科学的风险评估。
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Implementation of EPA Revised Cancer Assessment Guidelines: Incorporation of Mechanistic and Pharmacokinetic Data

A workshop entitled “Implementation of EPA Revised Cancer Assessment Guidelines: Incorporation of Mechanistic and Pharmacokinetic Data” was held in Anaheim, California, in 1996 at the 35th Annual Meeting of the Society of Toxicology (SOT). This workshop was jointly sponsored by the Carcinogenesis, Risk Assessment, and Veterinary Specialty Sections of the SOT. The thrust of the workshop was to discuss the scientific basis for the revisions to the EPA Guidelines for cancer assessment and EPA's plans for their implementation. This is the first revision to the original EPA guidelines which have been in use by EPA since 1986. The principal revisions are intended to provide a framework for an increased ability to incorporate biological data into the risk assessment process. Two cases were presented, for chloroform and trichloroethylene, that demonstrated the use of the revised guidelines for specific cancer risk assessments. Using these new guidelines, nonlinearmargin of exposureanalyses were proposed for these chemicals instead of thelinearized multistage modelpreviously used by the EPA as the default method. The workshop participants generally applauded the planned revisions to the EPA guidelines. For the most part, they considered that the revised guidelines represented a positive step which should allow for and encourage the use of biological information in the conduct of cancer risk assessments. Several participants cautioned however that the major problem with cancer risk assessments would continue to be the inadequacy of available data on which to conduct more scientific risk assessments.

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