PETA Science Consortium International e.V., Stuttgart, Germany.
Health Canada, Pest Management Regulatory Agency, Ottawa, Ontario, Canada.
Regul Toxicol Pharmacol. 2022 Jun;131:105160. doi: 10.1016/j.yrtph.2022.105160. Epub 2022 Mar 17.
Rodent cancer bioassays have been long-required studies for regulatory assessment of human cancer hazard and risk. These studies use hundreds of animals, are resource intensive, and certain aspects of these studies have limited human relevance. The past 10 years have seen an exponential growth of new technologies with the potential to effectively evaluate human cancer hazard and risk while reducing, refining, or replacing animal use. To streamline and facilitate uptake of new technologies, a workgroup comprised of scientists from government, academia, non-governmental organizations, and industry stakeholders developed a framework for waiver rationales of rodent cancer bioassays for consideration in agrochemical safety assessment. The workgroup used an iterative approach, incorporating regulatory agency feedback, and identifying critical information to be considered in a risk assessment-based weight of evidence determination of the need for rodent cancer bioassays. The reporting framework described herein was developed to support a chronic toxicity and carcinogenicity study waiver rationale, which includes information on use pattern(s), exposure scenario(s), pesticidal mode-of-action, physicochemical properties, metabolism, toxicokinetics, toxicological data including mechanistic data, and chemical read-across from similar registered pesticides. The framework could also be applied to endpoints other than chronic toxicity and carcinogenicity, and for chemicals other than agrochemicals.
啮齿类动物癌症生物测定一直是对人类癌症危害和风险进行监管评估的必要研究。这些研究使用了数百只动物,资源密集,并且这些研究的某些方面与人类相关性有限。过去十年中,新技术呈指数级增长,这些技术具有在减少、优化或替代动物使用的同时有效评估人类癌症危害和风险的潜力。为了简化和促进新技术的采用,一个由来自政府、学术界、非政府组织和行业利益相关者的科学家组成的工作组为农业化学品安全评估中的啮齿类动物癌症生物测定的豁免理由制定了一个框架。工作组采用了迭代方法,结合监管机构的反馈,并确定了在基于风险评估的证据权重确定啮齿类动物癌症生物测定必要性时需要考虑的关键信息。本文所述的报告框架旨在支持慢性毒性和致癌性研究豁免理由,其中包括使用模式、暴露情况、农药作用模式、物理化学性质、代谢、毒代动力学、毒理学数据(包括机制数据)以及来自类似注册农药的化学类推信息。该框架还可应用于除慢性毒性和致癌性以外的终点,以及除农业化学品以外的化学品。