Paranjpe Madhav G, Belich Jessica, Vidmar Tom J, Elbekai Reem H, McKeon Marie, Brown Caren
1 BioReliance By SAFC, Rockville, MD, USA.
2 BioSTAT Consultants, Inc., Portage, MI, USA.
Int J Toxicol. 2017 Jul/Aug;36(4):287-292. doi: 10.1177/1091581817707458. Epub 2017 May 28.
Our recent retrospective analysis of data, collected from 29 Tg.rasH2 mouse carcinogenicity studies, determined how successful the strategy of choosing the high dose for the 26-week studies was based on the estimated maximum tolerated dose (EMTD) derived from earlier 28-day dose range finding (DRF) studies conducted in CByB6F1 mice. Our analysis demonstrated that the high doses applied at EMTD in the 26-week Tg.rasH2 studies failed to detect carcinogenic effects. To investigate why the dose selection process failed in the 26-week carcinogenicity studies, the initial body weights, terminal body weights, body weight gains, food consumption, and mortality from the first 4 weeks of 26-week studies with Tg.rasH2 mice were compared with 28-day DRF studies conducted with CByB6F1 mice. Both the 26-week and the earlier respective 28-day studies were conducted with the exact same vehicle, test article, and similar dose levels. The analysis of our results further emphasizes that the EMTD and subsequent lower doses, determined on the basis of the 28-day studies in CByB6F1 mice, may not be an accurate strategy for selecting appropriate dose levels for the 26-week carcinogenicity studies in Tg.rasH2 mice. Based on the analysis presented in this article, we propose that the Tg.rasH2 mice and not the CByB6F1 mice should be used in future DRF studies. The Tg.rasH2 mice demonstrate more toxicity than the CByB6F1 mice, possibly because of their smaller size compared to CByB6F1 mice. Also, the Tg.rasH2 males appear to be more sensitive than the female Tg.rasH2 mice.
我们最近对从29项Tg.rasH2小鼠致癌性研究中收集的数据进行了回顾性分析,以确定在26周研究中基于在CByB6F1小鼠中进行的早期28天剂量范围查找(DRF)研究得出的估计最大耐受剂量(EMTD)来选择高剂量的策略有多成功。我们的分析表明,在26周Tg.rasH2研究中以EMTD应用的高剂量未能检测到致癌作用。为了调查为什么在26周致癌性研究中剂量选择过程失败,将Tg.rasH2小鼠26周研究前4周的初始体重、终末体重、体重增加、食物消耗和死亡率与用CByB6F1小鼠进行的28天DRF研究进行了比较。26周研究和早期各自的28天研究均使用完全相同的溶媒、受试物和相似的剂量水平。对我们结果的分析进一步强调,基于在CByB6F1小鼠中进行的28天研究确定的EMTD及随后的较低剂量,可能不是为Tg.rasH2小鼠的26周致癌性研究选择合适剂量水平的准确策略。基于本文中的分析,我们建议在未来的DRF研究中应使用Tg.rasH2小鼠而非CByB6F1小鼠。与CByB6F1小鼠相比,Tg.rasH2小鼠表现出更大的毒性,可能是因为其体型较小。此外,Tg.rasH2雄性小鼠似乎比雌性Tg.rasH2小鼠更敏感。