An indirect treatment comparison of the efficacy of insulin degludec/liraglutide (IDegLira) and insulin glargine/lixisenatide (iGlarLixi) in patients with type 2 diabetes uncontrolled on basal insulin

被引:25
|
作者
Evans, Marc [1 ]
Billings, Liana K. [2 ,3 ]
Hakan-Bloch, Jonas [4 ]
Slothuus, Ulla [4 ]
Abrahamsen, Trine J. [4 ]
Andersen, Andreas [4 ]
Jansen, Jeroen P. [5 ]
机构
[1] Univ Hosp Llandough, Cardiff, S Glam, Wales
[2] NorthShore Univ HealthSyst, Evanston, IL USA
[3] Univ Chicago, Pritzker Sch Med, Chicago, IL 60637 USA
[4] Novo Nordisk AS, Copenhagen, Denmark
[5] Precis Hlth Econ, Oakland, CA USA
关键词
GLP-1; basal insulin; glycemic control network meta-analysis; liraglutide; insulin analogs; FIXED-RATIO COMBINATION; GLARGINE PLUS LIXISENATIDE; GLP-1 RECEPTOR AGONISTS; TO-TARGET TRIAL; OPEN-LABEL; LIRAGLUTIDE IDEGLIRA; DEGLUDEC; METAANALYSIS; HYPOGLYCEMIA; MELLITUS;
D O I
10.1080/13696998.2017.1409228
中图分类号
F [经济];
学科分类号
02 ;
摘要
Aims: To obtain estimates of the relative treatment effects between insulin degludec/liraglutide (IDegLira) and insulin glargine U100/lixisenatide (iGlarLixi) in patients with type 2 diabetes mellitus (T2DM) uncontrolled on basal insulin therapy.Materials and methods: Data from phase 3 trials providing evidence for estimating the relative efficacy and safety of IDegLira vs iGlarLixi in patients uncontrolled on basal insulin-only regimens were used in this analysis. Outcomes of interest were changes in HbA(1c), body weight and insulin dose, and rate ratio of hypoglycemia. The indirect comparison of the reported trial findings followed the principles of Bucher etal.Results: IDegLira was estimated to provide a 0.44 [95% CI=0.17-0.71] %-point reduction in HbA(1c) compared with iGlarLixi. Body weight was reduced by 1.42 [95% CI=0.35-2.50] kg with IDegLira compared with iGlarLixi. Insulin dose was comparable between the two interventions. The rate of severe or blood glucose-confirmed (self-measured plasma glucose [SMPG]3.1mmol/L) hypoglycemia with IDegLira was approximately half that of iGlarLixi (rate ratio=0.51 [95% CI=0.29-0.90]). However, using the American Diabetes Association definition of documented symptomatic hypoglycemia (SMPG 3.9mmol/L) the rate was comparable between the two treatments (rate ratio=1.07 [95% CI=0.90-1.28]).Limitations: The assumptions made in the indirect comparison and differences between the included trials in baseline HbA(1c) levels, previous use of sulfonylureas, definitions of hypoglycemia, presence or absence of run-in period, the different duration of the trials, and the cross-over design of one of the trials.Conclusions: The results of this indirect treatment comparison demonstrate that, among patients with T2DM uncontrolled on basal insulin, treatment with IDegLira results in a greater reduction of HbA(1c) and a greater reduction in body weight compared with iGlarLixi at similar insulin doses.
引用
收藏
页码:340 / 347
页数:8
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