Hong Kong Orthopaedic and Osteoporosis Center for Treatment and Research, 6th Floor, Tower 2, New World Tower, 18 Queen's Road Central, Hong Kong, Hong Kong.
Amgen, Inc., Thousand Oaks, CA, USA.
Osteoporos Int. 2020 Apr;31(4):677-685. doi: 10.1007/s00198-020-05324-0. Epub 2020 Feb 11.
Romosozumab, a sclerostin antibody, exerts dual effect to increase bone formation and decrease bone resorption. Among high-risk postmenopausal East Asian women, romosozumab followed by alendronate was associated with lower incidences of fractures vs alendronate alone. Romosozumab demonstrates potential to address an unmet need in osteoporosis management in Asia.
Romosozumab, a sclerostin antibody, exerts dual effect to increase bone formation and decrease bone resorption. The global ARCH study demonstrated superiority of romosozumab followed by alendronate in reducing fracture risk in high-risk postmenopausal osteoporotic women vs alendronate alone. We report outcomes among ARCH East Asian patients.
In ARCH, 4093 postmenopausal osteoporotic women with fragility fracture were randomized 1:1 to monthly romosozumab 210 mg or weekly alendronate 70 mg for 12 months, both followed by open-label alendronate. Primary endpoints were incidence of new vertebral fracture (VF) at 24 months and clinical fracture at primary analysis (confirmed fractures in ≥ 330 patients and all patients had opportunity to attend month 24 visit). This post hoc analysis was not powered to detect fracture-rate differences.
This analysis included 275 patients from Hong Kong, Korea, and Taiwan. Romosozumab followed by alendronate reduced risk of new VFs at 24 months by 60% (P = 0.11) and clinical fractures at primary analysis by 44% (P = 0.15) vs alendronate alone. Romosozumab followed by alendronate significantly increased mean bone mineral density at 24 months from baseline by a further 9.0%, 3.3%, and 3.0% at the lumbar spine, total hip, and femoral neck vs alendronate alone. Adverse event (AE) rates, including positively adjudicated serious cardiovascular AEs (1.6% vs 1.4% at 12 months for romosozumab vs alendronate), were similar across treatment groups.
Consistent with the global analysis, romosozumab followed by alendronate was associated with lower incidences of new vertebral, clinical, non-vertebral, and hip fractures vs alendronate alone among East Asian patients.
罗莫索单抗是一种硬骨抑素抗体,具有增加骨形成和减少骨吸收的双重作用。在高风险的绝经后东亚女性中,与单独使用阿伦膦酸盐相比,罗莫索单抗联合阿伦膦酸盐可降低骨折发生率。罗莫索单抗在亚洲骨质疏松症管理中具有满足未满足需求的潜力。
罗莫索单抗是一种硬骨抑素抗体,具有增加骨形成和减少骨吸收的双重作用。全球 ARCH 研究表明,与单独使用阿伦膦酸盐相比,罗莫索单抗联合阿伦膦酸盐可降低高风险绝经后骨质疏松症女性的骨折风险。我们报告了 ARCH 东亚患者的结果。
在 ARCH 中,4093 名有脆性骨折史的绝经后骨质疏松症女性以 1:1 的比例随机接受每月 210mg 罗莫索单抗或每周 70mg 阿伦膦酸盐治疗 12 个月,两者均随后接受开放标签的阿伦膦酸盐治疗。主要终点是 24 个月时新发椎体骨折(VF)的发生率和主要分析时的临床骨折(≥330 例患者确诊骨折,所有患者均有机会参加 24 个月随访)。该事后分析未设效检验。
该分析包括来自香港、韩国和中国台湾的 275 名患者。与单独使用阿伦膦酸盐相比,罗莫索单抗联合阿伦膦酸盐可使 24 个月时新 VF 的风险降低 60%(P=0.11),主要分析时的临床骨折风险降低 44%(P=0.15)。与单独使用阿伦膦酸盐相比,罗莫索单抗联合阿伦膦酸盐在 24 个月时分别使腰椎、全髋关节和股骨颈的骨密度平均增加 9.0%、3.3%和 3.0%。治疗组的不良事件(AE)发生率相似,包括阳性判定的严重心血管不良事件(罗莫索单抗组为 1.6%,阿伦膦酸盐组为 1.4%,均为 12 个月时)。
与全球分析一致,与单独使用阿伦膦酸盐相比,在东亚患者中,罗莫索单抗联合阿伦膦酸盐可降低新发椎体、临床、非椎体和髋部骨折的发生率。