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DOI 10.1056/nejmoa0809493

Медицинская библиотека · The New England journal of medicine · 2009

Denosumab for prevention of fractures in postmenopausal women with osteoporosis.

Cummings Steven R, San Martin Javier, McClung Michael R, Siris Ethel S, Eastell Richard, Reid Ian R, Delmas Pierre, Zoog Holly B, Austin Matt, Wang Andrea, Kutilek Stepan, Adami Silvano, Zanchetta Jose, Libanati Cesar, Siddhanti Suresh, Christiansen Claus, FREEDOM Trial

СтатьяМногоцентровое исследованиеРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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.)

Для цитирования: Cummings Steven R, San Martin Javier, McClung Michael R, Siris Ethel S, Eastell Richard, Reid Ian R, Delmas Pierre, Zoog Holly B, Austin Matt, Wang Andrea, Kutilek Stepan, Adami Silvano, Zanchetta Jose, Libanati Cesar, Siddhanti Suresh, Christiansen Claus, FREEDOM Trial. Denosumab for prevention of fractures in postmenopausal women with osteoporosis.. The New England journal of medicine. 2009. DOI: 10.1056/nejmoa0809493.

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