University Department of Rheumatology, Lille Teaching Hospital, Lille, France.
Rheumatology (Oxford). 2009 Oct;48 Suppl 4:iv14-9. doi: 10.1093/rheumatology/kep275.
Given its increasing incidence and serious complications, osteoporosis requires safe and effective long-term treatment. Strontium ranelate (SR) is an osteoporosis treatment with a unique mode of action, which was launched in 2004. It has been investigated in the Spinal Osteoporosis Therapeutic Intervention (SOTI) and the TReatment Of Peripheral OSteoporosis (TROPOS) trials, two major 3-year multinational placebo-controlled Phase III randomized clinical trials. In SOTI, SR treatment reduced the risk of vertebral fracture by 41% (20.9 vs 32.8%; P < 0.001); in TROPOS, it reduced the risk of non-vertebral fracture by 16% (11.2 vs 12.9%; P = 0.04) and the risk of hip fracture in patients at high risk by 36% (4.3 vs 6.4%; P = 0.046). Unlike anti-resorptive agents, SR produced steady and significant BMD increases that correlated directly with decreases in vertebral and hip fracture risk. Preplanned analysis of the pooled dataset from SOTI and TROPOS showed that SR was effective whether or not patients had key risk factors for fractures at baseline. SR was also effective in patients with osteopenia and younger postmenopausal patients aged 50-65 years. Finally, SR significantly attenuated height loss and decreased back pain. The safety profile of SR was almost similar to placebo in both trials. Thus, SR demonstrates broad spectrum safety and efficacy in reducing the risks of both vertebral and non-vertebral (including hip) fractures in a wide variety of patients, and should be considered as a first-line option to treat women at risk of osteoporotic fractures, whatever their age, the severity of the disease and their risk factors.
鉴于其发病率不断上升和严重并发症,骨质疏松症需要安全有效的长期治疗。雷奈酸锶(SR)是一种具有独特作用机制的骨质疏松症治疗药物,于 2004 年上市。它已在两项主要的 3 年多国药典对照 III 期随机临床试验中得到研究,即脊柱骨质疏松治疗干预(SOTI)和外周骨质疏松治疗(TROPOS)试验。在 SOTI 中,SR 治疗将椎体骨折风险降低了 41%(20.9 比 32.8%;P<0.001);在 TROPOS 中,它将非椎体骨折风险降低了 16%(11.2 比 12.9%;P=0.04),并将高危患者髋部骨折风险降低了 36%(4.3 比 6.4%;P=0.046)。与抗吸收剂不同,SR 产生了稳定而显著的 BMD 增加,与椎体和髋部骨折风险的降低直接相关。对 SOTI 和 TROPOS 的汇总数据集进行的预先计划分析表明,无论患者基线时是否有骨折的关键危险因素,SR 都是有效的。SR 对骨量减少和年龄在 50-65 岁之间的年轻绝经后患者也有效。最后,SR 显著减轻了身高损失和背痛。在这两项试验中,SR 的安全性与安慰剂几乎相似。因此,SR 在降低各种患者的椎体和非椎体(包括髋部)骨折风险方面具有广泛的安全性和疗效,应被视为治疗有骨质疏松性骨折风险的女性的一线选择,无论其年龄、疾病严重程度和危险因素如何。