Department of General Medicine, Sengkang General Hospital, Singhealth, Singapore.
Duke NUS Medical School, Singapore.
Endocrinol Metab (Seoul). 2022 Apr;37(2):183-194. doi: 10.3803/EnM.2021.1369. Epub 2022 Apr 14.
Denosumab, which has been approved for the treatment of osteoporosis since 2010, is a fully humanised monoclonal antibody against a cytokine, receptor activator of nuclear factor kappa B ligand (RANKL), involved in bone resorption. Continued use of denosumab results in a potent and sustained decrease in bone turnover, an increase in bone mineral density (BMD), and a reduction in vertebral and hip fractures. The anti-resorptive effects of denosumab are reversible upon cessation, and this reversal is accompanied by a transient marked increase in bone turnover that is associated with bone loss, and of concern, an increased risk of multiple vertebral fractures. In this review, we outline the effects of denosumab withdrawal on bone turnover markers, BMD, histomorphometry, and fracture risk. We provide an update on recent clinical trials that sought to answer how clinicians can transition away from denosumab safely with follow-on therapy to mitigate bone loss and summarise the recommendations of various international guidelines.
地舒单抗自 2010 年以来被批准用于治疗骨质疏松症,它是一种针对核因子κB 配体受体激活剂(RANKL)的完全人源化单克隆抗体,该配体参与了骨吸收。地舒单抗的持续使用可导致骨转换的强效和持续降低、骨密度(BMD)增加以及椎体和髋部骨折减少。地舒单抗的抗吸收作用在停药后是可逆的,这种逆转伴随着骨转换的短暂明显增加,这与骨丢失有关,并且令人担忧的是,椎体骨折的风险增加。在这篇综述中,我们概述了地舒单抗停药对骨转换标志物、BMD、组织形态计量学和骨折风险的影响。我们提供了最近临床试验的最新信息,这些试验试图回答临床医生如何安全地从地舒单抗过渡到后续治疗以减轻骨丢失,并总结了各种国际指南的建议。