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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/16425


    Title: Therapeutic strategies of denosumab sequential therapy: A four-armed multi-institutional randomized controlled trial
    Authors: F, SH;L, CC;H, CC;L, CY;Y, HK;W, CY
    Contributors: National Center for Geriatrics and Welfare Research
    Abstract: Objective: Denosumab, a RANKL inhibitor, is renowned for its long-term efficacy in improving BMD and reducing fracture risks. However, its discontinuation leads to a rapid rebound and BMD loss, necessitating effective follow-up interventions. This study aimed to evaluate four treatment regimens post-denosumab discontinuation in patients with osteoporosis. Methods: The 2-y, multicenter, randomized controlled trial involved 101 postmenopausal women and men who had received biannual denosumab treatments for at least 2 y. The patients were randomized into four groups continued denosumab, zoledronate followed by denosumab, zoledronate for 2 y, and zoledronate followed by a supervised drug holiday. The primary outcome was the percent change from baseline at 24 months in BMD at various sites. Results: An alternating regimen of denosumab and zoledronate could lead to a BMD enhancement (LS-BMD, 2.25%; IQR, 0.02–5.82%). A strategically timed zoledronate injection can maintain BMD for two years post-denosumab (BMD at the lumbar spine [LS-BMD], -0.71%; interquartile range [IQR], − 3.67% to 2.69%). However, a single zoledronate dose post-denosumab brings significant BMD loss (LS-BMD, − 2.76%; IQR, − 6.12% to 2.06%). Conclusion: The study highlighted the "catch-up effect" in BMD upon resuming denosumab after a break, suggesting a potential reset in the body's response. Despite limitations like the short follow-up duration, the study provides novel insights into managing bone health post-denosumab discontinuation. Future studies should aim to validate the long-term therapeutic effect and the safety of the alternative regimen.
    Date: 2024-08-20
    Relation: Aging Clinical and Experimental Research. 2024 Aug 20;36:S265.
    Link to: http://dx.doi.org/10.1007/s40520-024-02766-y
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:001363175502220
    Appears in Collections:[王貞予] 會議論文/會議摘要

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