Department of Public Health and Health Economics, University of Liège, Liège, Belgium.
Osteoporos Int. 2012 Mar;23(3):1115-22. doi: 10.1007/s00198-011-1847-z. Epub 2011 Nov 29.
In an open-label extension study, BMD increased continuously with strontium ranelate over 10 years in osteoporotic women (P < 0.01). Vertebral and nonvertebral fracture incidence was lower between 5 and 10 years than in a matched placebo group over 5 years (P < 0.05). Strontium ranelate's antifracture efficacy appears to be maintained long term.
Strontium ranelate has proven efficacy against vertebral and nonvertebral fractures, including hip, over 5 years in postmenopausal osteoporosis. We explored long-term efficacy and safety of strontium ranelate over 10 years.
Postmenopausal osteoporotic women participating in the double-blind, placebo-controlled phase 3 studies SOTI and TROPOS to 5 years were invited to enter a 5-year open-label extension, during which they received strontium ranelate 2 g/day (n = 237, 10-year population). Bone mineral density (BMD) and fracture incidence were recorded, and FRAX® scores were calculated. The effect of strontium ranelate on fracture incidence was evaluated by comparison with a FRAX®-matched placebo group identified in the TROPOS placebo arm.
The patients in the 10-year population had baseline characteristics comparable to those of the total SOTI/TROPOS population. Over 10 years, lumbar BMD increased continuously and significantly (P < 0.01 versus previous year) with 34.5 ± 20.2% relative change from baseline to 10 years. The incidence of vertebral and nonvertebral fracture with strontium ranelate in the 10-year population in years 6 to 10 was comparable to the incidence between years 0 and 5, but was significantly lower than the incidence observed in the FRAX®-matched placebo group over 5 years (P < 0.05); relative risk reductions for vertebral and nonvertebral fractures were 35% and 38%, respectively. Strontium ranelate was safe and well tolerated over 10 years.
Long-term treatment with strontium ranelate is associated with sustained increases in BMD over 10 years, with a good safety profile. Our results also support the maintenance of antifracture efficacy over 10 years with strontium ranelate.
在一项开放标签延伸研究中,雷奈酸锶可使骨质疏松女性的骨密度持续增加,持续时间超过 10 年(P<0.01)。5 至 10 年期间,椎体和非椎体骨折的发生率低于 5 年时匹配安慰剂组(P<0.05)。雷奈酸锶的抗骨折疗效似乎长期保持。
雷奈酸锶对椎体和非椎体骨折(包括髋部骨折)具有 5 年以上的疗效,已在绝经后骨质疏松症中得到证实。我们探索了雷奈酸锶 10 年以上的长期疗效和安全性。
参加双盲、安慰剂对照的 SOTI 和 TROPOS 期 3 研究至 5 年的绝经后骨质疏松女性被邀请进入为期 5 年的开放标签延伸期,在此期间她们接受雷奈酸锶 2g/天(n=237,10 年人群)。记录骨密度(BMD)和骨折发生率,并计算 FRAX®评分。通过与 TROPOS 安慰剂组中根据 FRAX®匹配的安慰剂组进行比较,评估雷奈酸锶对骨折发生率的影响。
10 年人群的患者具有与 SOTI/TROPOS 总人群相似的基线特征。在 10 年期间,腰椎 BMD 持续显著增加(P<0.01,与前一年相比),与基线相比有 34.5±20.2%的相对变化至 10 年。在 10 年人群中,雷奈酸锶在第 6 至 10 年的椎体和非椎体骨折发生率与第 0 至 5 年的发生率相当,但明显低于 FRAX®匹配的安慰剂组在 5 年内的发生率(P<0.05);椎体和非椎体骨折的相对风险降低分别为 35%和 38%。雷奈酸锶在 10 年内安全且耐受性良好。
雷奈酸锶长期治疗可使 BMD 在 10 年内持续增加,安全性良好。我们的结果还支持雷奈酸锶在 10 年内保持抗骨折疗效。