Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.
J Bone Miner Res. 2020 Oct;35(10):1858-1870. doi: 10.1002/jbmr.4098. Epub 2020 Jul 12.
Discontinuing denosumab is associated with bone loss and possibly increased fracture risk. We investigated if treatment with zoledronate (ZOL) could prevent bone loss and if the timing of the ZOL infusion influenced the outcome. We report on a 2-year randomized, open label, interventional study including 61 patients with osteopenia, discontinuing denosumab after 4.6 ± 1.6 years. We administrated ZOL 6 months (6M group, n = 20) or 9 months (9M group, n = 20) after the last denosumab injection or when bone turnover had increased (OBS group, n = 21). We monitored the patients with DXA and bone turnover markers. Our primary endpoints were change in lumbar spine BMD (LSBMD) 6 months after ZOL and the proportion of patients who failed to maintain BMD. The study is ongoing (clinicaltrials.gov; NCT03087851). We included 61 participants and 59 patients completed follow-up 12 months after ZOL. Six months after ZOL, LSBMD had decreased significantly by (mean ± SE) 2.1% ± 0.9%, 4.3% ± 1.1%, and 3.0% ± 1.1% in the 6M, 9M, and OBS groups, respectively, and by 4.8% ± 0.7%, 4.1% ± 1.1%, and 4.7% ± 1.2% 12 months after ZOL in the 6M, 9M, and OBS groups, respectively (p < .02, no between-group differences). BMD loss above the least significant change was seen in all groups; at the spine: 6M, n = 6 (30%); 9M, n = 9 (45%); and OBS, n = 9 (47%); and at the total hip: 6M, n = 1 (5%); 9M, n = 5 (25%); and OBS, n = 2 (11%). In the 6M group p-crosslinked C-terminal telopeptide (p-CTX) decreased initially, but increased rapidly thereafter, and 6 months after ZOL, p-CTX was 0.60 ± 0.08 g/L. p-CTX increased rapidly in the 9M and OBS groups, was suppressed by ZOL but increased again thereafter; p-CTX was 0.47 ± 0.05 μg/L and 0.47 ± 0.05 μg/L in the 9M and OBS groups 6 months after ZOL, respectively. Incident vertebral fractures were seen in two women in the 9M group. Treatment with ZOL irrespective of the timing did not fully prevent loss of BMD in patients discontinuing denosumab. © 2020 American Society for Bone and Mineral Research.
停止使用地舒单抗会导致骨质流失,并可能增加骨折风险。我们研究了唑来膦酸(zoledronate,ZOL)治疗是否可以预防骨质流失,以及 ZOL 输注的时间是否会影响结果。我们报告了一项为期 2 年的随机、开放标签、干预性研究,纳入了 61 例骨质疏松症患者,在使用地舒单抗 4.6±1.6 年后停止使用。我们在最后一次地舒单抗注射后 6 个月(6M 组,n=20)或 9 个月(9M 组,n=20)或骨转换增加时(OBS 组,n=21)给予 ZOL。我们通过双能 X 线吸收法(DXA)和骨转换标志物监测患者。我们的主要终点是 ZOL 后 6 个月腰椎骨密度(lumbar spine bone mineral density,LSBMD)的变化和无法维持骨密度的患者比例。该研究正在进行中(clinicaltrials.gov;NCT03087851)。我们纳入了 61 名参与者,59 名患者在 ZOL 后 12 个月完成了随访。ZOL 后 6 个月,6M、9M 和 OBS 组的 LSBMD 分别显著下降(均值±SE)2.1%±0.9%、4.3%±1.1%和 3.0%±1.1%,6M、9M 和 OBS 组的 LSBMD 分别在 ZOL 后 12 个月时下降了 4.8%±0.7%、4.1%±1.1%和 4.7%±1.2%(p<0.02,组间无差异)。所有组均出现了骨密度损失超过最小有意义变化(least significant change,LS)的情况;在脊柱:6M 组,n=6(30%);9M 组,n=9(45%);和 OBS 组,n=9(47%);在总髋部:6M 组,n=1(5%);9M 组,n=5(25%);和 OBS 组,n=2(11%)。在 6M 组中,p 环交联 C 端肽(p-crosslinked C-terminal telopeptide,p-CTX)最初下降,但随后迅速增加,ZOL 后 6 个月,p-CTX 为 0.60±0.08μg/L。9M 和 OBS 组中的 p-CTX 迅速增加,被 ZOL 抑制,但随后再次增加;9M 和 OBS 组在 ZOL 后 6 个月时的 p-CTX 分别为 0.47±0.05μg/L 和 0.47±0.05μg/L。在 9M 组中有 2 名女性发生了新发椎体骨折。无论 ZOL 的时间如何,使用 ZOL 治疗都不能完全防止停止使用地舒单抗的患者的骨密度丢失。© 2020 美国骨矿研究协会。