Felter Susan P, Bhat Virunya S, Botham Philip A, Bussard David A, Casey Warren, Hayes A Wallace, Hilton Gina M, Magurany Kelly A, Sauer Ursula G, Ohanian Edward V
Procter & Gamble, Mason, OH, USA.
ToxStrategies, Inc., Boston, MA, USA.
Crit Rev Toxicol. 2021 Sep;51(8):653-694. doi: 10.1080/10408444.2021.2003295. Epub 2022 Jan 4.
The Toxicology Forum convened an international state-of-the-science workshop in December 2020. Challenges related to assessing chemical carcinogenicity were organized under the topics of (1) problem formulation; (2) modes-of-action; (3) dose-response assessment; and (4) the use of new approach methodologies (NAMs). Key topics included the mechanisms of genotoxic and non-genotoxic carcinogenicity and how these in conjunction with consideration of exposure conditions might inform dose-response assessments and an overall risk assessment; approaches to evaluate the human relevance of modes-of-action observed in rodent studies; and the characterization of uncertainties. While the scientific limitations of the traditional rodent chronic bioassay were widely acknowledged, knowledge gaps that need to be overcome to facilitate the further development and uptake of NAMs were also identified. Since one single NAM is unlikely to replace the bioassay, activities to combine NAMs into integrated approaches for testing and assessment, or preferably into defined approaches for testing and assessment that include data interpretation procedures, were identified as urgent research needs. In addition, adverse outcome pathway networks can provide a framework for organizing the available evidence/data for assessing chemical carcinogenicity. Since a formally accepted decision tree to guide use of the best and most current science to advance carcinogenicity risk assessment is currently unavailable, a Decision Matrix for carcinogenicity assessment could be useful. The workshop organizers developed and presented a decision matrix to be considered within a carcinogenicity hazard and risk assessment that is offered in tabular form.
毒理学论坛于2020年12月召开了一次国际科学现状研讨会。与评估化学致癌性相关的挑战按照以下主题进行组织:(1) 问题设定;(2) 作用模式;(3) 剂量反应评估;以及(4) 新方法学(NAMs)的应用。关键主题包括遗传毒性和非遗传毒性致癌性的机制,以及这些机制如何与暴露条件的考虑相结合,从而为剂量反应评估和整体风险评估提供信息;评估在啮齿动物研究中观察到的作用模式与人类相关性的方法;以及不确定性的特征描述。虽然传统啮齿动物慢性生物测定的科学局限性得到了广泛认可,但也确定了为促进NAMs的进一步发展和应用而需要克服的知识空白。由于单一的NAM不太可能取代生物测定,将NAMs整合为综合测试和评估方法,或者更理想的是整合为包括数据解释程序的确定测试和评估方法的活动,被确定为迫切的研究需求。此外,不良结局途径网络可为组织评估化学致癌性的现有证据/数据提供框架。由于目前没有一个正式认可的决策树来指导使用最佳和最新科学进展进行致癌性风险评估,一个致癌性评估决策矩阵可能会有所帮助。研讨会组织者制定并展示了一个以表格形式呈现的、用于致癌性危害和风险评估时考虑的决策矩阵。