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在接受地舒单抗治疗的患者中,发生骨折后再次发生骨质疏松性骨折的风险降低:来自 FREEDOM 和 FREEDOM 扩展研究的结果。

The risk of subsequent osteoporotic fractures is decreased in subjects experiencing fracture while on denosumab: results from the FREEDOM and FREEDOM Extension studies.

机构信息

University of British Columbia, Vancouver, BC, Canada.

Amgen Inc., Thousand Oaks, CA, USA.

出版信息

Osteoporos Int. 2019 Jan;30(1):71-78. doi: 10.1007/s00198-018-4687-2. Epub 2018 Sep 22.

Abstract

UNLABELLED

This post-hoc analysis queried whether women experiencing fracture on denosumab indicates inadequate treatment response or whether the risk of subsequent fracture remains low with continuing denosumab. Results showed that denosumab decreases the risk of subsequent fracture and fracture sustained while on denosumab is not necessarily indicative of inadequate treatment response.

INTRODUCTION

This analysis assessed whether a fracture sustained during denosumab therapy indicates inadequate treatment response and if the risk of a subsequent fracture decreases with continuing denosumab treatment.

METHODS

In FREEDOM, a clinical trial to evaluate the efficacy and safety of denosumab, postmenopausal women with osteoporosis were randomized to placebo or denosumab for 3 years. In the 7-year FREEDOM Extension, all participants were allocated to receive denosumab. Here we compare subsequent osteoporotic fracture rates between denosumab-treated subjects during FREEDOM or the Extension and placebo-treated subjects in FREEDOM.

RESULTS

During FREEDOM, 438 placebo- and 272 denosumab-treated subjects had an osteoporotic fracture. Exposure-adjusted subject incidence per 100 subject-years was lower for denosumab (6.7) vs placebo (10.1). Combining all subjects on denosumab from FREEDOM and the Extension for up to 10 years (combined denosumab), 794 (13.7%) had an osteoporotic fracture while on denosumab. Of these, one or more subsequent fractures occurred in 144 (18.1%) subjects, with an exposure-adjusted incidence of 5.8 per 100 subject-years, similar to FREEDOM denosumab (6.7 per 100 subject-years) and lower than FREEDOM placebo (10.1 per 100 subject-years). Adjusting for prior fracture, the risk of having a subsequent on-study osteoporotic fracture was lower in the combined denosumab group vs placebo (hazard ratio [95% CI]: 0.59 [0.43-0.81]; P = 0.0012).

CONCLUSIONS

These data demonstrate that denosumab decreases the risk of subsequent fracture and a fracture sustained while on denosumab is not necessarily indicative of inadequate treatment response.

摘要

未标注

本事后分析旨在探讨接受地舒单抗治疗后发生骨折的患者是否提示治疗应答不足,以及继续使用地舒单抗治疗是否会降低随后发生骨折的风险。结果表明,地舒单抗可降低随后发生骨折的风险,且在接受地舒单抗治疗期间发生的骨折不一定表明治疗应答不足。

引言

本分析评估了在接受地舒单抗治疗期间发生的骨折是否提示治疗应答不足,以及继续使用地舒单抗治疗是否会降低随后发生骨折的风险。

方法

在评估地舒单抗疗效和安全性的 FREEDOM 临床试验中,绝经后骨质疏松症患者被随机分配至安慰剂或地舒单抗组,接受为期 3 年的治疗。在 FREEDOM 7 年扩展研究中,所有患者均接受地舒单抗治疗。本研究比较了 FREEDOM 扩展研究期间以及 FREEDOM 研究中地舒单抗治疗组和安慰剂治疗组患者的后续骨质疏松性骨折发生率。

结果

FREEDOM 研究期间,安慰剂组和地舒单抗组分别有 438 例和 272 例患者发生骨质疏松性骨折。地舒单抗组调整后的患者发生率(每 100 名患者年 6.7 例)低于安慰剂组(每 100 名患者年 10.1 例)。将 FREEDOM 研究和扩展研究期间所有接受地舒单抗治疗的患者(联合地舒单抗)的最长 10 年数据合并,共有 794 例(13.7%)患者发生骨质疏松性骨折。其中,144 例(18.1%)患者发生了 1 次或多次后续骨折,调整后的发生率为每 100 名患者年 5.8 例,与 FREEDOM 研究中的地舒单抗组(6.7 例)相似,且低于 FREEDOM 研究中的安慰剂组(10.1 例)。调整骨折发生情况后,联合地舒单抗组患者发生后续研究期间骨质疏松性骨折的风险低于安慰剂组(风险比[95%CI]:0.59[0.43-0.81];P=0.0012)。

结论

这些数据表明,地舒单抗可降低随后发生骨折的风险,且在接受地舒单抗治疗期间发生的骨折不一定表明治疗应答不足。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2f7/6331737/c1f46887c354/198_2018_4687_Fig1_HTML.jpg

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