Suppr超能文献

评估LY2963016甘精胰岛素与来得时®甘精胰岛素在1型或2型糖尿病患者中的免疫原性。

Evaluation of immunogenicity of LY2963016 insulin glargine compared with Lantus® insulin glargine in patients with type 1 or type 2 diabetes mellitus.

作者信息

Ilag L L, Deeg M A, Costigan T, Hollander P, Blevins T C, Edelman S V, Konrad R J, Ortmann R A, Pollom R K, Huster W J, Zielonka J S, Prince M J

机构信息

Eli Lilly and Company, Indianapolis, IN, USA.

Baylor Endocrine Center, Dallas, TX, USA.

出版信息

Diabetes Obes Metab. 2016 Feb;18(2):159-68. doi: 10.1111/dom.12584. Epub 2016 Jan 8.

Abstract

AIMS

To compare the immunogenicity profiles and the potential effects on clinical outcomes of LY2963016 insulin glargine (LY IGlar) and Lantus® insulin glargine (IGlar), products with identical primary amino acid sequences, in patients with type 1 or type 2 diabetes mellitus (T1DM or T2DM).

METHODS

To assess immunogenicity, anti-insulin glargine antibodies (measured as percent binding) were compared between treatments in 52-week (open-label) and 24-week (double-blind) randomized studies in total study populations of patients with T1DM (N = 535) and T2DM (N = 756), respectively, and two subgroups of patients with T2DM: insulin-naïve patients and those reporting prestudy IGlar treatment (prior IGlar). Relationships between insulin antibody levels and clinical outcomes were assessed using analysis of covariance and partial correlations. Insulin antibody levels were assessed using Wilcoxon rank sum. Treatment comparisons for treatment-emergent antibody response (TEAR) and incidence of detectable antibodies were analysed using Fisher's exact test.

RESULTS

No significant treatment differences were observed for insulin antibody levels, incidence of detectable anti-insulin glargine antibodies, or incidence of TEAR [overall and endpoint, by last-observation-carried-forward (LOCF)] in patients with T1DM or patients with T2DM, including the insulin-naïve subgroup. A statistically significant difference was noted in the overall incidence of detectable antibodies but not at endpoint (LOCF) nor in TEAR for the prior IGlar subgroup of patients with T2DM. Insulin antibody levels were low (<5%) in both treatment groups. Insulin antibody levels or developing TEAR was not associated with clinical outcomes.

CONCLUSIONS

LY IGlar and IGlar have similar immunogenicity profiles; anti-insulin glargine antibody levels were low for both treatments, with no observed effect on efficacy and safety outcomes.

摘要

目的

比较具有相同一级氨基酸序列的LY2963016甘精胰岛素(LY IGlar)和来得时®甘精胰岛素(IGlar)在1型或2型糖尿病(T1DM或T2DM)患者中的免疫原性特征以及对临床结局的潜在影响。

方法

为评估免疫原性,在分别针对T1DM患者(N = 535)和T2DM患者(N = 756)的52周(开放标签)和24周(双盲)随机研究的总研究人群中,以及T2DM患者的两个亚组:初治胰岛素患者和报告研究前使用IGlar治疗的患者(既往使用IGlar)中,比较各治疗组间的抗甘精胰岛素抗体(以结合百分比衡量)。使用协方差分析和偏相关分析评估胰岛素抗体水平与临床结局之间的关系。使用Wilcoxon秩和检验评估胰岛素抗体水平。使用Fisher精确检验分析治疗出现的抗体反应(TEAR)和可检测抗体发生率的治疗组间比较。

结果

在T1DM患者或T2DM患者(包括初治胰岛素亚组)中,胰岛素抗体水平、可检测的抗甘精胰岛素抗体发生率或TEAR发生率[总体和终点,采用末次观察结转(LOCF)法]均未观察到显著的治疗差异。对于T2DM既往使用IGlar亚组患者,可检测抗体总体发生率存在统计学显著差异,但终点(LOCF)时或TEAR方面无差异。两个治疗组的胰岛素抗体水平均较低(<5%)。胰岛素抗体水平或出现TEAR与临床结局无关。

结论

LY IGlar和IGlar具有相似的免疫原性特征;两种治疗的抗甘精胰岛素抗体水平均较低,未观察到对疗效和安全性结局的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dbd/4737399/bace79a6ff5e/DOM-18-159-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验