Goodman Julie, Lynch Heather
Gradient, 20 University Road, Cambridge, MA 02138, United States.
Gradient, 20 University Road, Cambridge, MA 02138, United States.
Toxicol Appl Pharmacol. 2017 Mar 15;319:39-46. doi: 10.1016/j.taap.2017.01.020. Epub 2017 Feb 3.
The International Agency for Research on Cancer (IARC) recently developed a framework for evaluating mechanistic evidence that includes a list of 10 key characteristics of carcinogens. This framework is useful for identifying and organizing large bodies of literature on carcinogenic mechanisms, but it lacks sufficient guidance for conducting evaluations that fully integrate mechanistic evidence into hazard assessments.
We summarize the framework, and suggest approaches to strengthen the evaluation of mechanistic evidence using this framework.
While the framework is useful for organizing mechanistic evidence, its lack of guidance for implementation limits its utility for understanding human carcinogenic potential. Specifically, it does not include explicit guidance for evaluating the biological significance of mechanistic endpoints, inter- and intra-individual variability, or study quality and relevance. It also does not explicitly address how mechanistic evidence should be integrated with other realms of evidence. Because mechanistic evidence is critical to understanding human cancer hazards, we recommend that IARC develop transparent and systematic guidelines for the use of this framework so that mechanistic evidence will be evaluated and integrated in a robust manner, and concurrently with other realms of evidence, to reach a final human cancer hazard conclusion.
IARC does not currently provide a standardized approach to evaluating mechanistic evidence. Incorporating the recommendations discussed here will make IARC analyses of mechanistic evidence more transparent, and lead to assessments of cancer hazards that reflect the weight of the scientific evidence and allow for scientifically defensible decision-making.
国际癌症研究机构(IARC)最近制定了一个评估机制证据的框架,其中包括一份致癌物的10个关键特征清单。该框架有助于识别和整理大量关于致癌机制的文献,但在将机制证据充分纳入危害评估的评估过程中缺乏足够的指导。
我们总结该框架,并提出使用此框架加强机制证据评估的方法。
虽然该框架有助于整理机制证据,但其缺乏实施指导限制了其在理解人类致癌潜力方面的效用。具体而言,它没有包括评估机制终点的生物学意义、个体间和个体内变异性或研究质量和相关性的明确指导。它也没有明确说明机制证据应如何与其他证据领域相结合。由于机制证据对于理解人类癌症危害至关重要,我们建议IARC制定使用该框架的透明且系统的指南,以便以有力的方式评估和整合机制证据,并与其他证据领域同时进行,以得出最终的人类癌症危害结论。
IARC目前没有提供评估机制证据的标准化方法。纳入此处讨论的建议将使IARC对机制证据的分析更加透明,并导致对癌症危害的评估反映科学证据的权重,并允许进行具有科学依据的决策。