sanofi-aventis Deutschland GmbH, DSAR/Business Division Diabetes, D-65926 Frankfurt am Main, Frankfurt, Germany.
Int J Toxicol. 2012 Mar;31(2):137-42. doi: 10.1177/1091581811431111. Epub 2012 Jan 3.
The 1995 to 1997 lifetime carcinogenicity studies of insulin glargine in rats and mice were reanalyzed and reassessed for their validity according to current guidelines. In 2-year studies, 50 animals per sex and per group were used. Survival rates between weeks 80 and 90 in female mice and rats were greater than 20 animals in all groups, fulfilling current Food and Drug Administration requirements that enough animals lived long enough to provide adequate exposure to glargine and to be at risk of forming late-developing tumors. Exposure to 5 or 12.5 IU/kg glargine was similar to or 2 to 3 times greater than 5 IU/kg neutral protamine Hagedorn insulin, respectively. Using statistical methods recommended by current guidelines, no significant effect of glargine on mammary gland neoplastic lesions in female rodents was found, confirming earlier results. Thus, both studies can be considered valid according to contemporary standards. Insulin glargine does not present a carcinogenic risk.
根据当前指南,对胰岛素甘精在大鼠和小鼠中的 1995 年至 1997 年终生致癌性研究进行了重新分析和评估。在为期两年的研究中,每组使用 50 只雌雄动物。在雌性小鼠和大鼠中,第 80 至 90 周的存活率在所有组中均大于 20 只,这满足了当前食品和药物管理局的要求,即足够的动物存活时间足够长,以提供对甘精的充分暴露,并有可能形成晚期发展的肿瘤。接受 5 或 12.5IU/kg 甘精的暴露与接受 5IU/kg 中性鱼精蛋白 Hagedorn 胰岛素的暴露相似,或分别为 2 至 3 倍。使用当前指南推荐的统计方法,未发现甘精对雌性啮齿动物乳腺肿瘤病变有显著影响,这证实了早期的结果。因此,根据当代标准,这两项研究均可被认为是有效的。胰岛素甘精不存在致癌风险。