Denosumab for Prevention of Fractures in Postmenopausal Women with Osteoporosis

德诺苏马布 医学 兰克尔 骨质疏松症 骨吸收 激活剂(遗传学) 秩配基 单克隆抗体 单克隆 绝经后妇女 骨密度保护剂 内科学 骨矿物 内分泌学 绝经后骨质疏松症 受体 抗体 免疫学
作者
Steven R. Cummings,Javier San Martín,Michael R. McClung,Ethel S. Siris,Richard Eastell,Ian R. Reid,Pierre Delmas,Holly Brenza Zoog,Matt Austin,Andrea Wang,Štěpán Kutílek,Silvano Adami,José Zanchetta,Cesar Libanati,Suresh Siddhanti,Claus Christiansen
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:361 (8): 756-765 被引量:3479
标识
DOI:10.1056/nejmoa0809493
摘要

BACKGROUND: Denosumab is a fully human monoclonal antibody to the receptor activator of nuclear factor-kappaB ligand (RANKL) that blocks its binding to RANK, inhibiting the development and activity of osteoclasts, decreasing bone resorption, and increasing bone density. Given its unique actions, denosumab may be useful in the treatment of osteoporosis. METHODS: We enrolled 7868 women between the ages of 60 and 90 years who had a bone mineral density T score of less than -2.5 but not less than -4.0 at the lumbar spine or total hip. Subjects were randomly assigned to receive either 60 mg of denosumab or placebo subcutaneously every 6 months for 36 months. The primary end point was new vertebral fracture. Secondary end points included nonvertebral and hip fractures. RESULTS: As compared with placebo, denosumab reduced the risk of new radiographic vertebral fracture, with a cumulative incidence of 2.3% in the denosumab group, versus 7.2% in the placebo group (risk ratio, 0.32; 95% confidence interval [CI], 0.26 to 0.41; P<0.001)--a relative decrease of 68%. Denosumab reduced the risk of hip fracture, with a cumulative incidence of 0.7% in the denosumab group, versus 1.2% in the placebo group (hazard ratio, 0.60; 95% CI, 0.37 to 0.97; P=0.04)--a relative decrease of 40%. Denosumab also reduced the risk of nonvertebral fracture, with a cumulative incidence of 6.5% in the denosumab group, versus 8.0% in the placebo group (hazard ratio, 0.80; 95% CI, 0.67 to 0.95; P=0.01)--a relative decrease of 20%. There was no increase in the risk of cancer, infection, cardiovascular disease, delayed fracture healing, or hypocalcemia, and there were no cases of osteonecrosis of the jaw and no adverse reactions to the injection of denosumab. CONCLUSIONS: Denosumab given subcutaneously twice yearly for 36 months was associated with a reduction in the risk of vertebral, nonvertebral, and hip fractures in women with osteoporosis. (ClinicalTrials.gov number, NCT00089791.)
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