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停止地舒单抗治疗。

Stopping Denosumab.

机构信息

Center of Bone Diseases, Lausanne University Hospital, Lausanne, Switzerland.

Service of Internal Medicine, CHUV, Lausanne University Hospital, Rue du Bugnon 46, CH-1011, Lausanne, Switzerland.

出版信息

Curr Osteoporos Rep. 2019 Feb;17(1):8-15. doi: 10.1007/s11914-019-00502-4.

Abstract

PURPOSE OF REVIEW

Denosumab discontinuation is associated with a rebound effect manifesting by an increased risk of multiple spontaneous vertebral fractures. The purpose of this review is to (1) better characterize this risk and (2) find solutions to avoid it.

RECENT FINDINGS

In the absence of a potent bisphosphonate prescription at denosumab discontinuation, the frequency of multiple vertebral fractures is common or frequent (≥ 1/100 and < 1/10). In five recent case series, the median number of vertebral fractures was 5 within 7 to 20 months (median 11) after the last denosumab injection. Prescribing bisphosphonate before starting denosumab and/or after stopping denosumab may reduce this risk. However, only small case series have evaluated these strategies. After the second denosumab dose, there is a rebound effect with an increased risk of multiple vertebral fractures. A potent bisphosphonate prescribed at denosumab discontinuation could reduce this risk. As denosumab discontinuation is characterized by many uncertainties, denosumab is a second-line treatment for osteoporosis. Studies are urgently needed to define the management of denosumab discontinuation.

摘要

目的综述

地舒单抗停药后会出现反弹效应,表现为自发性多发椎体骨折风险增加。本文旨在:(1) 更准确地描述这种风险;(2) 寻找避免该风险的方法。

最近的发现

在停止使用地舒单抗时未开具强效双膦酸盐处方的情况下,多发椎体骨折的频率较高或频繁(≥ 1/100 且 < 1/10)。在最近的五项病例系列研究中,末次地舒单抗注射后 7 至 20 个月(中位数 11 个月)内,椎体骨折中位数为 5 例。在开始使用地舒单抗之前和/或停止使用地舒单抗后开具双膦酸盐可能会降低这种风险。但是,仅有少数病例系列研究评估了这些策略。在接受第二剂地舒单抗后,会出现反弹效应,增加多发椎体骨折的风险。在停止使用地舒单抗时开具强效双膦酸盐可能会降低这种风险。由于地舒单抗停药存在许多不确定因素,因此地舒单抗是骨质疏松症的二线治疗药物。迫切需要开展研究来明确地舒单抗停药的管理方法。

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