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EPA transparency proposal: testimony of Edward J. Calabrese Ph.D October 3 2018

机译:EPA透明度提案:Edward J.Calabrese博士的证词2018年10月3日

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摘要

The historical foundations of cancer risk assessment and its adoption by the US EPA in the mid 1970s were based on the discovery of X-ray-induced gene mutations by Hermann J. Muller, its transformation into the linear nonthreshold (LNT) single-hit theory and the recommendations of the model by the US National Academy of Sciences, Biological Effects of Atomic/Ionizing Radiation, Genetics Panels in 1956 and 1972. This testimony summarizes substantial recent revelations which profoundly challenge the use of LNT as a default in cancer risk assessment, showing multiple significant scientific errors and incorrect interpretations, mixed with deliberate misrepresentation of the scientific record by leading ideologically motivated radiation geneticists. These novel historical and scientific findings demonstrate that the scientific foundations of the LNT single-hit model were seriously flawed and should not have been adopted for cancer risk assessment. The testimony supports the recommendation by the EPA to move away from the use of the LNT as a default in cancer risk assessment and to the formal consideration of alternative dose response models such as the threshold, hormetic and other non-linear modeling approaches.
机译:癌症风险评估及其在1970年代中期被美国EPA采纳的历史基础是基于Hermann J. Muller对X射线诱导的基因突变的发现,并将其转化为线性非阈值(LNT)单击理论以及美国国家科学院,原子/电离辐射的生物效应,遗传学小组分别于1956年和1972年提出的模型建议。该证词总结了近期的大量启示,这些启示深刻挑战了将LNT作为癌症风险评估中的默认方法,表现出多种重大的科学错误和错误的解释,以及由意识形态驱动的辐射遗传学家对科学记录的故意歪曲。这些新颖的历史和科学发现表明,LNT单发攻击模型的科学基础存在严重缺陷,不应将其用于癌症风险评估。证词支持EPA的建议,不再使用LNT作为癌症风险评估的默认方法,而正式考虑替代剂量反应模型,例如阈值,钟表和其他非线性建模方法。

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