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双膦酸盐药物假期:来自临床试验和真实世界研究的证据。

Bisphosphonate Drug Holidays: Evidence From Clinical Trials and Real-World Studies.

作者信息

Wang Mawson, Wu Yu-Fang, Girgis Christian M

机构信息

Department of Diabetes and Endocrinology Westmead Hospital Westmead NSW Australia.

Faculty of Medicine and Health University of Sydney Sydney NSW Australia.

出版信息

JBMR Plus. 2022 May 24;6(6):e10629. doi: 10.1002/jbm4.10629. eCollection 2022 Jun.

Abstract

Bisphosphonates (BPs) are commonly used in the treatment of osteoporosis and are effective in the prevention of fragility fracture. Long-term use has been associated with the development of atypical femur fractures (AFFs) and osteonecrosis of the jaw (ONJ). Drug holidays seek to reduce the risk of insufficiency fractures (AFFs) while maintaining durable effects of long-term treatment in the prevention of fragility fracture. Guidelines suggest that BP drug holidays be considered after 3 to 5 years. However individual factors impacting this decision and outcomes are unclear. This review examines key factors in the planning of a safe BP drug holiday and surrogate markers of fracture risk in patients discontinuing treatment. Fifteen randomized control trials and 19 real-world studies were included, including nationwide prospective studies from several countries. Increases in bone turnover markers (BTMs) and reductions in bone mineral density (BMD) were generally observed during BP drug holidays. Resurgent bone turnover was problematic in high-risk patients in whom fractures recurred as early as 12 months following a drug holiday. Risk factors for holiday-related fractures included older age, low hip BMD, underweight, low medication adherence, and prevalent/incident fractures. Zoledronic acid conferred the most durable reduction in fractures, particularly after six annual infusions. Five years of alendronate was insufficient in preventing vertebral fractures in high-risk patients embarking on a drug holiday. Relatively faster offset of antiresorptive effect was seen in risedronate users with more frequent fractures than alendronate during a drug holiday. Studies directly counterbalancing effects of long-term treatment on AFF risk versus drug holiday outcomes in the same population were lacking. In the absence of persistently high fracture risk and following a specific treatment duration dependent on the BP used, drug holidays are safe and mitigate the risk of AFF. However, anti-resorptive effects diminish over time; ongoing monitoring and careful planning of BP resumption is necessary. © 2022 The Authors. published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.

摘要

双膦酸盐(BPs)常用于治疗骨质疏松症,对预防脆性骨折有效。长期使用与非典型股骨骨折(AFFs)和颌骨坏死(ONJ)的发生有关。药物假期旨在降低不全骨折(AFFs)的风险,同时在预防脆性骨折方面维持长期治疗的持久效果。指南建议在3至5年后考虑双膦酸盐药物假期。然而,影响这一决策和结果的个体因素尚不清楚。本综述探讨了安全的双膦酸盐药物假期规划中的关键因素以及停止治疗患者骨折风险的替代标志物。纳入了15项随机对照试验和19项真实世界研究,包括来自几个国家的全国性前瞻性研究。在双膦酸盐药物假期期间,通常观察到骨转换标志物(BTMs)增加和骨密度(BMD)降低。骨转换复苏在高危患者中是个问题,这些患者在药物假期后最早12个月就会再次发生骨折。与假期相关骨折的风险因素包括年龄较大、髋部骨密度低、体重过轻、药物依从性差以及既往/新发骨折。唑来膦酸在降低骨折方面的效果最持久,尤其是在每年输注6次之后。对于开始药物假期的高危患者,五年的阿仑膦酸钠不足以预防椎体骨折。在药物假期期间,与阿仑膦酸钠相比,使用利塞膦酸钠且骨折更频繁的患者抗吸收作用的抵消相对更快。缺乏在同一人群中直接权衡长期治疗对AFF风险与药物假期结果影响的研究。在没有持续高骨折风险且经过取决于所用双膦酸盐的特定治疗持续时间后,药物假期是安全的,并可降低AFF的风险。然而,抗吸收作用会随着时间减弱;持续监测和仔细规划双膦酸盐的重新使用是必要的。© 2022作者。由Wiley Periodicals LLC代表美国骨与矿物质研究学会出版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1be/9189912/b85077caff91/JBM4-6-e10629-g001.jpg

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