Denosumab for Prevention of Fractures in Postmenopausal Women with Osteoporosis

被引:2366
作者
Cummings, Steven R. [1 ,2 ]
San Martin, Javier [3 ]
McClung, Michael R. [4 ]
Siris, Ethel S. [5 ]
Eastell, Richard [6 ]
Reid, Ian R. [7 ]
Delmas, Pierre [8 ,9 ]
Zoog, Holly B. [3 ]
Austin, Matt [3 ]
Wang, Andrea [3 ]
Kutilek, Stepan [10 ]
Adami, Silvano [11 ]
Zanchetta, Jose [12 ,13 ]
Libanati, Cesar [3 ,14 ]
Siddhanti, Suresh [3 ]
Christiansen, Claus
机构
[1] Calif Pacific Med Ctr, Res Inst, San Francisco Coordinating Ctr, San Francisco, CA USA
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
[3] Amgen Inc, Thousand Oaks, CA USA
[4] Oregon Osteoporosis Ctr, Portland, OR USA
[5] Columbia Univ, Med Ctr, New York, NY USA
[6] Univ Sheffield, Sheffield, S Yorkshire, England
[7] Univ Auckland, Auckland 1, New Zealand
[8] Univ Lyon, Lyon, France
[9] INSERM, Res Unit 831, F-69008 Lyon, France
[10] Ctr Clin & Basic Res, Pardubice, Czech Republic
[11] Univ Verona, I-37100 Verona, Italy
[12] Inst Invest Metab, Buenos Aires, DF, Argentina
[13] Univ Salvador, Buenos Aires, DF, Argentina
[14] Ctr Clin & Basic Res, Ballerup, Denmark
关键词
BONE-MINERAL DENSITY; NONVERTEBRAL FRACTURES; VERTEBRAL FRACTURES; RANDOMIZED-TRIAL; RISK; RISEDRONATE; ALENDRONATE; THERAPY; TURNOVER; LONG;
D O I
10.1056/NEJMoa0809493
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Denosumab is a fully human monoclonal antibody to the receptor activator of nuclear factor-kappa B 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.)
引用
收藏
页码:756 / 765
页数:10
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