Further Nonvertebral Fracture Reduction Beyond 3 Years for Up to 10 Years of Denosumab Treatment

被引:25
作者
Ferrari, Serge [1 ]
Butler, Peter W. [2 ]
Kendler, David L. [3 ]
Miller, Paul D. [4 ]
Roux, Christian [5 ]
Wang, Andrea T. [2 ]
Huang, Shuang [2 ]
Wagman, Rachel B. [2 ]
Lewiecki, E. Michael [6 ]
机构
[1] Geneva Univ Hosp, CH-1205 Geneva, Switzerland
[2] Amgen Inc, Thousand Oaks, CA 91320 USA
[3] Univ British Columbia, Vancouver, BC V6T 1Z4, Canada
[4] Colorado Ctr Bone Res, Lakewood, CO 80227 USA
[5] Paris Descartes Univ, F-75006 Paris, France
[6] New Mexico Clin Res & Osteoporosis Ctr, Albuquerque, NM 87106 USA
关键词
QUALITY-OF-LIFE; POSTMENOPAUSAL WOMEN; ZOLEDRONIC ACID; VERTEBRAL FRACTURES; ECONOMIC BURDEN; OSTEOPOROSIS; TRIAL; ALENDRONATE; RISK; DISCONTINUATION;
D O I
10.1210/jc.2019-00271
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Evidence for further nonvertebral fracture (NVF) reductions with long-term antiresorptive therapy in osteoporosis is lacking. Objective: To evaluate NVF risk reduction in subjects receiving <= 10 years of denosumab treatment. Design: Phase 3, randomized, placebo-controlled, 3-year Fracture Reduction Evaluation of Denosumab in Osteoporosis Every 6 Months (FREEDOM) trial (NCT00089791) and its open-label 7-year extension (NCT00523341). Setting: One hundred seventy-two study centers worldwide. Patients: Women 60 to 90 years, lumbar spine or total hip bone mineral density T-scores < -2.5( >=-4.0 at both). Interventions: Subjects randomly assigned 1:1 denosumab 60 mg SC Q6M (long-term) or placebo (crossover) in FREEDOM; eligible subjects could enroll in the extension to receive denosumab 60 mg SC Q6M. Main Outcome Measures: NVF Exposure-adjusted subject incidence (per 100 subject-years) during denosumab treatment years 1 to 3 and 4 to 7 (all subjects) and years 4 to 10 (long-term only), and rate ratios (RRs) for years 4 to 7 or 4 to 10 vs 1 to 3. Results: Among 4074 subjects (2343 long-term, 1731 crossover), NVF rates (95% CI) in all subjects were 2.15 (1.90 to 2.43) during years 1 to 3 and 1.53 (1.34 to 1.75) during years 4 to 7 of denosumab treatment [RR (95% CI) = 0.72 (0.61 to 0.86); P < 0.001]; in long-term only were 1.98 (1.67 to 2.34) during years 1 to 3 and 1.44 (1.24 to 1.66) during years 4 to 10 [RR = 0.74 (0.60 to 0.93); P = 0.008]. combined osteonecrosis of the jaw and atypical femoral fracture rate was 0.06. Conclusions: Long-term denosumab treatment, >3 and <= 10 years, was associated with further reductions in NVF rates compared with the first 3 years.
引用
收藏
页码:3450 / 3461
页数:12
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