Scripps Whittier Diabetes Institute, La Jolla, California.
Sanofi, Bridgewater, New Jersey.
J Diabetes. 2019 Dec;11(12):971-981. doi: 10.1111/1753-0407.12952. Epub 2019 Jun 26.
This study compared the efficacy and safety of lixisenatide with placebo as add-on therapy to basal insulin (BI) in adults aged ≥70 years with type 2 diabetes (T2D), with or without moderate renal insufficiency.
This post hoc analysis evaluated data from non-frail patients with T2D inadequately controlled on BI with or without oral antidiabetic drugs (n = 108), randomized to once-daily lixisenatide 20 μg or placebo for 24 weeks (GetGoal-O Study). The primary endpoint was the change in HbA1c from baseline to Week 24. Secondary endpoints included changes from baseline in fasting plasma glucose, 2-hour postprandial plasma glucose (PPG), average seven-point self-monitored plasma glucose (SMPG), area under the curve for SMPG, daily BI dose, body weight, proportion of patients achieving HbA1c > 0.5%, and composite endpoints. Safety outcomes included the incidence of documented symptomatic hypoglycemia (plasma glucose <60 mg/dL) and gastrointestinal treatment-emergent adverse events (TEAEs). Outcomes were also analyzed by the occurrence of moderate renal insufficiency.
Compared with placebo, lixisenatide-treated patients had significantly greater reductions in HbA1c, 2-hour PPG, average seven-point SMPG, and body weight. Documented symptomatic hypoglycemia was approximately two-fold higher in patients treated with placebo than lixisenatide (12.7% vs 5.7%). GI TEAEs occurred more frequently in the lixisenatide- than placebo-treated group (34% vs 9.1%). Moderate renal insufficiency (estimated glomerular filtration rate between ≥30 and <60 mL/min/1.73 m ) did not negatively affect lixisenatide efficacy or safety. A greater proportion of patients treated with lixisenatide than placebo achieved composite endpoints.
Add-on therapy with lixisenatide in non-frail patients aged ≥70 years with T2D uncontrolled with BI is effective, safe, and well tolerated and should be considered in this population.
本研究比较了利西拉肽与安慰剂作为基础胰岛素(BI)添加治疗药物,在年龄≥70 岁、有或无中度肾功能不全的 2 型糖尿病(T2D)成人中的疗效和安全性。
这项事后分析评估了来自 T2D 患者的数据,这些患者在接受 BI 治疗的情况下血糖控制不佳,同时还接受或未接受口服降糖药物治疗(n=108),他们被随机分为每日一次 20μg 利西拉肽或安慰剂组,治疗 24 周(GetGoal-O 研究)。主要终点是从基线到第 24 周时 HbA1c 的变化。次要终点包括从基线开始的空腹血糖、餐后 2 小时血糖、平均七点自我监测血糖、平均七点自我监测血糖曲线下面积、每日 BI 剂量、体重、HbA1c>0.5%的患者比例以及复合终点。安全性结果包括记录到的有症状低血糖(血糖<60mg/dL)和胃肠道治疗相关不良事件(TEAEs)的发生率。还根据中度肾功能不全的发生情况分析了结局。
与安慰剂相比,利西拉肽治疗患者的 HbA1c、餐后 2 小时血糖、平均七点自我监测血糖和体重均显著降低。接受安慰剂治疗的患者发生记录到的有症状低血糖的比例大约是接受利西拉肽治疗的患者的两倍(12.7% vs 5.7%)。利西拉肽治疗组胃肠道 TEAEs 的发生率高于安慰剂治疗组(34% vs 9.1%)。中度肾功能不全(估计肾小球滤过率为≥30 至<60ml/min/1.73m )并不影响利西拉肽的疗效或安全性。接受利西拉肽治疗的患者中有更大比例达到复合终点。
在年龄≥70 岁、BI 控制不佳的 T2D 患者中,添加利西拉肽治疗是有效、安全且耐受良好的,在该人群中应考虑使用。