Denosumab Treatment in Postmenopausal Women with Osteoporosis Does Not Interfere with Fracture-Healing Results from the FREEDOM Trial

被引:91
作者
Adami, Silvano [1 ]
Libanati, Cesar [2 ]
Boonen, Steven [3 ]
Cummings, Steven R. [4 ,5 ]
Ho, Pei-Ran [2 ]
Wang, Andrea [2 ]
Siris, Ethel [6 ]
Lane, Joseph [7 ]
机构
[1] Univ Verona, Fac Med & Surg, I-37134 Verona, Italy
[2] Amgen Inc, Thousand Oaks, CA 91320 USA
[3] Univ Louvain, Dept Expt Med, Bone Res Unit, B-3000 Louvain, Belgium
[4] Calif Pacific Med Ctr, Res Inst, San Francisco Coordinating Ctr, San Francisco, CA 94107 USA
[5] Univ Calif San Francisco, San Francisco, CA 94107 USA
[6] Columbia Univ, Med Ctr, Dept Med, New York, NY 10032 USA
[7] Hosp Special Surg, Dept Orthoped Surg, New York, NY 10021 USA
关键词
BONE-MINERAL DENSITY; HIP FRACTURE; SUBSEQUENT FRACTURES; OLDER-ADULTS; TURNOVER; THERAPY; BISPHOSPHONATES; MORTALITY; ALENDRONATE; RANKL;
D O I
10.2106/JBJS.K.00774
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Background: Fracture is the major complication of osteoporosis, and it allows the identification of individuals needing medical intervention for osteoporosis. After nonvertebral fracture, patients often do not receive osteoporosis medical treatment despite evidence that this treatment reduces the risk of subsequent fracture. In this preplanned analysis of the results of the three-year, placebo-controlled FREEDOM trial, we evaluated the effect of denosumab administration on fracture-healing to address theoretical concerns related to initiating or continuing denosumab therapy in patients presenting with a nonvertebral fracture. Methods: Postmenopausal women aged sixty to ninety years with osteoporosis were randomized to receive 60 mg of denosumab (n = 3902) or a placebo (n = 3906) subcutaneously every six months for three years. Investigators reported complications associated with a fracture or its management and with fracture-healing for all nonvertebral fractures that occurred during the study. Delayed healing was defined as incomplete fracture-healing six months after the fracture. Results: Six hundred and sixty-seven subjects (303 treated with denosumab and 364 who received a placebo) had a total of 851 nonvertebral fractures (386 in the denosumab group and 465 in the placebo group), including 199 fractures (seventy-nine in the denosumab group and 120 in the placebo group) that were treated surgically. Delayed healing was reported in seven subjects (two in the denosumab group and five in the placebo group), including one with subsequent nonunion (in the placebo group). Neither delayed healing nor nonunion was observed in any subject who had received denosumab within six weeks preceding or following the fracture. A complication associated with the fracture or intervention occurred in five subjects (2%) and twenty subjects (5%) in the denosumab and placebo groups, respectively (p = 0.009). Conclusions: Denosumab in a dose of 60 mg every six months does not seem to delay fracture-healing or contribute to other complications, even when it is administered at or near the time of the fracture.
引用
收藏
页码:2113 / 2119
页数:7
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