Discontinuation of Denosumab therapy for osteoporosis: A systematic review and position statement by ECTS

被引:347
作者
Tsourdi, Elena [1 ,2 ]
Langdahl, Bente [3 ]
Cohen-Solal, Martine [4 ,5 ,6 ]
Aubry-Rozier, Berengere [7 ]
Eriksen, Erik Fink [8 ]
Guanabens, Nuria [9 ]
Obermayer-Pietsch, Barbara [10 ,11 ]
Ralston, Stuart H. [12 ]
Eastell, Richard [13 ]
Zillikens, M. Carola [14 ]
机构
[1] Tech Univ Dresden, Dept Med 3, Dresden, Germany
[2] Tech Univ Dresden, Ctr Hlth Aging, Dresden, Germany
[3] Aarhus Univ Hosp, Med Dept Endocrinol, Aarhus, Denmark
[4] INSERM, U1132, Paris, France
[5] Univ Paris Diderot, Paris, France
[6] Lariboisiere Hosp, Dept Rheumatol, Paris, France
[7] Lausanne Univ Hosp, Ctr Bone Dis, Lausanne, Switzerland
[8] Univ Oslo, Inst Clin Med, Oslo Univ Hosp, Dept Clin Endocrinol Morbid Obes & Prevent Med, Oslo, Norway
[9] Univ Barcelona, IDIBAPS, CIBERehd, Dept Rheumatol,Metab Bone Dis Unit,Hosp Clin, Barcelona, Spain
[10] Med Univ Graz, Div Endocrinol & Diabetol, Dept Internal Med, Graz, Austria
[11] Ctr Biomarker Res Med CBmed, Graz, Austria
[12] Univ Edinburgh, Western Gen Hosp, Ctr Genom & Expt Med, MRC,Inst Genet & Mol Med, Edinburgh, Midlothian, Scotland
[13] Univ Sheffield, Mellanby Ctr Bone Res, Sheffield, S Yorkshire, England
[14] Erasmus MC, Dept Internal Med, Bone Ctr, Rotterdam, Netherlands
关键词
Osteoporbsis treatment; Denosumab; Discontinuation; Fractures; Position paper; POSTMENOPAUSAL WOMEN; VERTEBRAL FRACTURES; TERIPARATIDE; BISPHOSPHONATES; REDUCTION; EXTENSION; MEN;
D O I
10.1016/j.bone.2017.08.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The optimal duration of osteoporosis treatment is controversial. As opposed to bisphosphonates, denosumab does not incorporate into bone matrix and bone turnover is not suppressed after its cessation. Recent reports imply that denosumab discontinuation may lead to an increased risk of multiple vertebral fractures. Methods: The European Calcified Tissue Society (ECTS) formed a working group to perform a systematic review of existing literature on the effects of stopping denosumab and provide advice on management. Results: Data from phase 2 and 3 clinical trials underscore a rapid decrease of bone mineral density (BMD) and a steep increase in bone turnover markers (BTMs) after discontinuation of denosumab. Clinical case series report multiple vertebral fractures after discontinuation of denosumab and a renewed analysis of FREEDOM and FREEDOM Extension Trial suggests, albeit does not prove, that the risk of multiple vertebral fractures may be increased when denosumab is stopped due to a rebound increase in bone resorption. Conclusion: There appears to be an increased risk of multiple vertebral fractures after discontinuation of denosumab although strong evidence for such an effect and for measures to prevent the occurring bone loss is lacking. Clinicians and patients should be aware of this potential risk. Based on available data, a reevaluation should be performed after 5 years of denosumab treatment. Patients considered at high fracture risk should either continue denosumab therapy for up to 10 years or be switched to an alternative treatment. For patients at low risk, a decision to discontinue denosumab could be made after 5 years, but bisphosphonate therapy should be considered to reduce or prevent the rebound increase in bone turnover. However, since the optimal bisphosphonate regimen post-denosumab is currently unknown continuation of denosumab can also be considered until results from ongoing trials become available. Based on current data, denosumab should not be stopped without considering alternative treatment in order to prevent rapid BMD loss and a potential rebound in vertebral fracture risk. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:11 / 17
页数:7
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