Department of Internal Medicine, Randers Regional Hospital, Randers, Denmark.
Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.
J Bone Miner Res. 2021 Jul;36(7):1245-1254. doi: 10.1002/jbmr.4305. Epub 2021 Apr 20.
Increased bone turnover and rapid bone loss follow discontinuation of denosumab. We investigated the long-term efficacy of zoledronate (ZOL) in maintaining bone mineral density (BMD) after discontinuation of denosumab. In this randomized, open-label, interventional study, we included 61 postmenopausal women and men older than 50 years discontinuing denosumab after 4.6 ± 1.6 years. We administered ZOL 6 months (6 M) or 9 months (9 M) after the last denosumab or when bone turnover had increased (observation group [OBS]). ZOL was readministrated if p-cross-linked C-terminal telopeptide (p-CTX) increased ≥1.26 μg/L or BMD decreased ≥5%. The results after 12 months have previously been published; here we report the outcome after 24 months (ClinicalTrials NCT03087851). Fifty-eight patients completed the study. From 12 to 24 months after the initial ZOL, lumbar spine (LS) BMD was maintained: 0.9 ± 0.9%, 0.4 ± 0.8%, and 0.3 ± 0.7% in the 6 M, 9 M, and OBS groups, respectively (p > .05, no between-group differences). Similarly, total hip (TH) and femoral neck (FN) BMD did not change in any group during year 2. From baseline to 24 months after ZOL, LS BMD decreased by 4.0 ± 0.8%, 4.1 ± 0.8%, and 4.3 ± 1.5% in the 6 M, 9 M, and OBS groups, respectively (p < .001, no between-group differences). Significant bone loss (LS, TH, or FN) was found in all groups 24 months after ZOL: 6 M group: n = 12 (60%), 9 M group: n = 7 (37%), and OBS group: n = 10 (53%). P-CTX did not change significantly during the second year (p > .05, no between-group differences). No patient fulfilled the CTX or fracture criteria for retreatment during year 2; however, 9 patients were retreated at M24 due to BMD loss ≥5%. Two patients sustained a non-vertebral fracture during year 2. Treatment with ZOL subsequent to long-term denosumab did not fully prevent increased bone turnover and bone loss during the first year; however, CTX remained with the reference range and BMD was maintained during the second year. © 2021 American Society for Bone and Mineral Research (ASBMR).
地舒单抗停药后会出现骨转换增加和骨快速丢失。我们研究了唑来膦酸(zoledronate,ZOL)在停用地舒单抗后维持骨密度(bone mineral density,BMD)的长期疗效。在这项随机、开放标签、干预性研究中,我们纳入了 61 名绝经后女性和 50 岁以上的男性,这些患者在接受地舒单抗治疗 4.6±1.6 年后停药。我们在最后一次地舒单抗治疗后 6 个月(6M)或 9 个月(9M)或在骨转换增加时(观察组[observation group,OBS])给予 ZOL。如果 p 交联 C 端肽(p-cross-linked C-terminal telopeptide,p-CTX)增加≥1.26μg/L 或 BMD 降低≥5%,则重新给予 ZOL。此前我们已经报道了 12 个月的研究结果;在此,我们报告了 24 个月(ClinicalTrials NCT03087851)的研究结果。58 名患者完成了这项研究。在初始 ZOL 治疗后 12 至 24 个月时,腰椎(lumbar spine,LS)BMD 保持稳定:6M、9M 和 OBS 组分别为 0.9±0.9%、0.4±0.8%和 0.3±0.7%(p>.05,无组间差异)。同样,TH 和 FN 的 BMD 在任何组中在第 2 年均未发生变化。从基线到 ZOL 治疗后 24 个月时,LS BMD 在 6M、9M 和 OBS 组中分别下降了 4.0±0.8%、4.1±0.8%和 4.3±1.5%(p<.001,无组间差异)。在 ZOL 治疗后 24 个月时,所有组均出现显著的骨丢失(LS、TH 或 FN):6M 组:n=12(60%)、9M 组:n=7(37%)和 OBS 组:n=10(53%)。第二年 p-CTX 无显著变化(p>.05,无组间差异)。第二年没有患者达到 CTX 或骨折的再治疗标准;然而,有 9 名患者因 BMD 丢失≥5%而在 M24 时进行了再治疗。2 名患者在第 2 年发生非椎体骨折。在长期接受地舒单抗治疗后使用 ZOL 治疗并未完全预防第 1 年中骨转换的增加和骨丢失;然而,CTX 仍在参考范围内,BMD 在第 2 年保持稳定。2021 年美国骨与矿物质研究协会(American Society for Bone and Mineral Research,ASBMR)。