Colorado Center for Bone Research, 3190 S Wadsworth Blvd, Lakewood, CO, 80227, USA,
Osteoporos Int. 2014 Jan;25(1):349-57. doi: 10.1007/s00198-013-2518-z. Epub 2013 Oct 18.
Ibandronate reduces the risk of vertebral and non-vertebral fractures versus placebo in postmenopausal women with osteoporosis. This analysis, in which fractures were reported as safety events, showed that long-term use of ibandronate was associated with low fracture rates over 5 years of treatment.
A previous post-hoc meta-analysis of 2-3 year studies found that ibandronate regimens with annual cumulative exposure (ACE) of ≥10.8 mg reduced the risk of vertebral and nonvertebral fractures (NVFs) versus placebo in postmenopausal women. This post-hoc analysis used individual patient data from the 2-year monthly oral ibandronate in ladies (MOBILE) and dosing intravenous administration (DIVA) studies, including the 3-year long-term extensions (LTEs), to assess fracture risk in patients treated with ibandronate for 5 years.
Patients treated for 2 years in MOBILE with monthly oral ibandronate 150 mg (n = 176) and in DIVA with IV ibandronate every 2 months 2 mg (n = 253) or quarterly 3 mg (n = 263) who continued on the same regimens for 3 additional years in the LTEs were included. Three-year placebo data (n = 1,924) were obtained from the ibandronate osteoporosis vertebral fracture trial in North America and Europe (BONE) and IV Fracture Prevention trials. The primary endpoint was clinical fracture rate; clinical fracture data were collected as adverse events. Time to fracture was analyzed using Kaplan-Meier and statistical analysis was conducted using the log-rank test. All clinical fractures included all NVFs and symptomatic vertebral fractures.
For ibandronate regimens with ACE ≥10.8 mg, time to fracture was significantly longer for all clinical fractures, NVFs, and clinical vertebral fractures versus placebo (P = 0.005). For all fracture types, the rate of fracture appeared stable during the 5-year treatment period.
In women with postmenopausal osteoporosis, continuous treatment with ibandronate over 5 years results in low sustained clinical fracture rate.
与安慰剂相比,伊班膦酸盐可降低绝经后骨质疏松症妇女的椎体和非椎体骨折风险。这项分析报告了骨折作为安全性事件,表明长期使用伊班膦酸盐与治疗 5 年内的低骨折率相关。
之前对 2-3 年研究的事后荟萃分析发现,伊班膦酸盐方案的年累积暴露(ACE)≥10.8mg 可降低绝经后妇女的椎体和非椎体骨折(NVF)风险,与安慰剂相比。这项事后分析使用了来自 2 年每月口服伊班膦酸盐在女士(MOBILE)和剂量静脉给药(DIVA)研究的个体患者数据,包括 3 年的长期扩展(LTE),以评估接受伊班膦酸盐治疗 5 年的患者的骨折风险。
在 MOBILE 中接受 2 年治疗的患者每月口服伊班膦酸盐 150mg(n=176),在 DIVA 中接受每 2 个月静脉注射伊班膦酸盐 2mg(n=253)或每季度 3mg(n=263),在 LTE 中继续使用相同的方案治疗 3 年。从北美和欧洲的伊班膦酸盐骨质疏松性椎体骨折试验(BONE)和 IV 骨折预防试验获得了 3 年安慰剂数据(n=1924)。主要终点是临床骨折率;临床骨折数据作为不良事件收集。使用 Kaplan-Meier 分析骨折时间,使用对数秩检验进行统计分析。所有临床骨折均包括所有 NVF 和有症状椎体骨折。
对于 ACE≥10.8mg 的伊班膦酸盐方案,所有临床骨折、NVF 和临床椎体骨折的骨折时间明显长于安慰剂(P=0.005)。对于所有骨折类型,在 5 年治疗期间,骨折发生率似乎保持稳定。
在绝经后骨质疏松症妇女中,连续 5 年使用伊班膦酸盐治疗可导致持续的低临床骨折率。