Faculty of Medicine & Surgery, University of Verona, P. le Scuro 10, 37134, Verona, Italy.
J Bone Joint Surg Am. 2012 Dec 5;94(23):2113-9. doi: 10.2106/JBJS.K.00774.
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 pre planned 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.
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.
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).
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.
骨折是骨质疏松症的主要并发症,它可以识别需要接受骨质疏松症医学治疗的个体。发生非椎体骨折后,尽管有证据表明这种治疗可降低后续骨折的风险,但患者往往未接受骨质疏松症治疗。在这项为期三年、安慰剂对照的 FREEDOM 试验的预先计划分析中,我们评估了 denosumab 给药对骨折愈合的影响,以解决与在发生非椎体骨折的患者中开始或继续 denosumab 治疗相关的理论问题。
年龄在 60 岁至 90 岁之间的绝经后骨质疏松症女性随机接受 60 mg denosumab(n = 3902)或安慰剂(n = 3906)皮下注射,每六个月一次,持续三年。研究者报告了与骨折或其管理以及所有研究期间发生的非椎体骨折愈合相关的并发症。延迟愈合定义为骨折后 6 个月时骨折未完全愈合。
667 名受试者(denosumab 治疗 303 名,安慰剂组 364 名)共发生 851 例非椎体骨折(denosumab 组 386 例,安慰剂组 465 例),其中 199 例(denosumab 组 79 例,安慰剂组 120 例)接受手术治疗。报告了 7 例(denosumab 组 2 例,安慰剂组 5 例)延迟愈合,包括 1 例(安慰剂组)发生后续骨不连。在骨折前或后 6 周内接受 denosumab 的任何患者均未观察到延迟愈合或骨不连。在 denosumab 和安慰剂组,分别有 5 名(2%)和 20 名(5%)受试者发生与骨折或干预相关的并发症(p = 0.009)。
每六个月给予 60 mg 的 denosumab 似乎不会延迟骨折愈合或导致其他并发症,即使在骨折时或附近给予该药物。