Further reductions in nonvertebral fracture rate with long-term denosumab treatment in the FREEDOM open-label extension and influence of hip bone mineral density after 3 years

被引:56
作者
Ferrari, S. [1 ]
Adachi, J. D. [2 ]
Lippuner, K. [3 ]
Zapalowski, C. [4 ]
Miller, P. D. [5 ]
Reginster, J. -Y. [6 ]
Torring, O. [7 ]
Kendler, D. L. [8 ]
Daizadeh, N. S. [4 ]
Wang, A. [4 ]
O'Malley, C. D. [4 ]
Wagman, R. B. [4 ]
Libanati, C. [4 ]
Lewiecki, E. M. [9 ,10 ]
机构
[1] Univ Hosp Geneva, Geneva, Switzerland
[2] McMaster Univ, Hamilton, ON, Canada
[3] Univ Hosp Bern, CH-3010 Bern, Switzerland
[4] Amgen Inc, Thousand Oaks, CA 91320 USA
[5] Colorado Ctr Bone Res, Lakewood, CO USA
[6] Univ Liege, Liege, Belgium
[7] Karolinska Inst, Stockholm, Sweden
[8] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
[9] New Mexico Clin Res, Albuquerque, NM USA
[10] Osteoporosis Ctr, Albuquerque, NM USA
关键词
Denosumab; Fracture threshold; Hip bone mineral density; Long-term osteoporosis therapy; Nonvertebral fracture; Treatment to goal; OVARIECTOMIZED CYNOMOLGUS MONKEYS; HUMAN RANKL ANTIBODY; POSTMENOPAUSAL OSTEOPOROSIS; INTERVENTION TRIAL; RANDOMIZED-TRIAL; VERTEBRAL FRACTURES; ZOLEDRONIC ACID; WOMEN; ALENDRONATE; RISK;
D O I
10.1007/s00198-015-3179-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Limited data exist on the efficacy of long-term therapies for osteoporosis. In osteoporotic postmenopausal women receiving denosumab for 7 years, nonvertebral fracture rates significantly decreased in years 4-7 versus years 1-3. This is the first demonstration of a further benefit on fracture outcomes with long-term therapy for osteoporosis. Introduction This study aimed to evaluate whether denosumab treatment continued beyond 3 years is associated with a further reduction in nonvertebral fracture rates. Methods Participants who completed the 3-year placebo-controlled Fracture REduction Evaluation of Denosumab in Osteoporosis every 6 Months (FREEDOM) study were invited to participate in an open-label extension. The present analysis includes 4,074 postmenopausal women with osteoporosis (n = 2,343 long-term; n = 1,731 cross-over) who enrolled in the extension, missed = 1 dose during their first 3 years of denosumab treatment, and continued into the fourth year of treatment. Comparison of nonvertebral fracture rates during years 1-3 of denosumab with that of the fourth year and with the rate during years 4-7 was evaluated. Results For the combined group, the nonvertebral fracture rate per 100 participant-years was 2.15 for the first 3 years of denosumab treatment (referent) and 1.36 in the fourth year (rate ratio [RR] = 0.64; 95 % confidence interval (CI) = 0.48 to 0.85, p = 0.003). Comparable findings were observed in the groups separately and when nonvertebral fracture rates during years 1-3 were compared to years 4-7 in the long-term group (RR = 0.79; 95 % CI = 0.62 to 1.00, p = 0.046). Fracture rate reductions in year 4 were most prominent in subjects with persisting low hip bone mineral density (BMD). Conclusions Denosumab treatment beyond 3 years was associated with a further reduction in nonvertebral fracture rate that persisted through 7 years of continuous denosumab administration. The degree to which denosumab further reduces nonvertebral fracture risk appears influenced by the hip bone density achieved with initial therapy.
引用
收藏
页码:2763 / 2771
页数:9
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