首页> 美国卫生研究院文献>Therapeutic Advances in Musculoskeletal Disease >Bazedoxifene: the evolving role of third-generation selective estrogen-receptor modulators in the management of postmenopausal osteoporosis
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Bazedoxifene: the evolving role of third-generation selective estrogen-receptor modulators in the management of postmenopausal osteoporosis

机译:Bazedoxifene:第三代选择性雌激素受体调节剂在绝经后骨质疏松症管理中的作用

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摘要

Osteoporosis is a significant public health concern, particularly for postmenopausal women. Current treatment options may not be appropriate for all women. Selective estrogen-receptor modulators (SERMs) are a class of molecules with tissue-selective activity. Bazedoxifene is currently in clinical development for the prevention and treatment of postmenopausal osteoporosis. In a 2-year, phase III, osteoporosis prevention study (N = 1583), bazedoxifene 10, 20, and 40 mg was shown to preserve bone mineral density and decrease biochemical markers of bone turnover compared with placebo in postmenopausal women at risk for osteoporosis. In a pivotal 3-year, phase III, osteoporosis treatment study (N = 7492), bazedoxifene 20 and 40 mg significantly reduced the incidence of new vertebral fractures compared with placebo (p < 0.05 for both) in postmenopausal women with osteoporosis. In a post hoc subgroup analysis of women at higher risk for fracture (n = 1772), bazedoxifene 20 mg significantly reduced the risk of nonvertebral fractures versus placebo (p = 0.02) and raloxifene 60 mg (p = 0.05). Bazedoxifene 20 mg has demonstrated sustained efficacy in reducing the risk of vertebral fractures over 5 and 7 years. Overall, bazedoxifene was generally safe and well tolerated, with favorable endometrial and breast safety profiles. As with other SERMs, the rate of deep vein thrombosis was higher in the bazedoxifene groups compared with placebo at 3 and 5 years. Considering its demonstrated efficacy and safety, bazedoxifene may be an appropriate osteoporosis therapy for women who cannot take or are unwilling to take bisphosphonates because of safety or tolerability issues. Bazedoxifene may also be appropriate for younger women at increased fracture risk who are concerned about the effects of long-term bisphosphonate therapy. This article reviews the results of key clinical trials of bazedoxifene for the prevention and treatment of postmenopausal osteoporosis and describes its role in clinical practice.
机译:骨质疏松症是一个重大的公共卫生问题,尤其是对于绝经后妇女。当前的治疗方案可能并不适合所有女性。选择性雌激素受体调节剂(SERM)是一类具有组织选择性活性的分子。 Bazedoxifene目前正在临床上用于预防和治疗绝经后骨质疏松症。在一项为期2年的III期骨质疏松症预防研究中(N = 1583),与安慰剂相比,在有骨质疏松症风险的绝经后妇女中,巴多昔芬10、20和40mg可以保持骨矿物质密度并降低骨转换的生化指标。 。在一项关键的为期3年的III期骨质疏松症治疗研究中(N = 7492),与安慰剂相比,苯卓昔芬20和40mg显着降低了绝经后骨质疏松症妇女的新椎体骨折的发生率(两者均p <0.05)。在有较高骨折风险的妇女(n = 1772)的事后亚组分析中,与安慰剂(p = 0.02)和雷洛昔芬60 mg(p = 0.05)相比,巴多昔芬20 mg显着降低了非椎骨骨折的风险。 Bazedoxifene 20 mg在5年和7年中一直显示出持续降低椎骨骨折风险的功效。总体而言,巴多昔芬是安全的且耐受性良好,子宫内膜和乳房的安全性良好。与其他SERM一样,在3年和5年时,巴多昔芬组的深静脉血栓形成率高于安慰剂组。考虑到其已证明的疗效和安全性,巴多昔芬对于因安全或耐受性问题而不能服用或不愿意服用双膦酸盐的妇女可能是一种合适的骨质疏松疗法。 Bazedoxifene也可能适合年轻的骨折风险较高的年轻妇女,她们担心长期使用双膦酸盐治疗的效果。本文回顾了巴多昔芬预防和治疗绝经后骨质疏松症的关键临床试验结果,并描述了其在临床实践中的作用。

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