唑来膦酸钠对长期地诺单抗治疗后骨密度和骨转换的影响:在现实世界环境中的观察。

Bone Pub Date : 2022-07-01 DOI:10.2139/ssrn.4106277
J. Everts‐Graber, S. Reichenbach, B. Gahl, H. Häuselmann, H. Ziswiler, U. Studer, Thomas Lehmann
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引用次数: 7

摘要

背景停药后的反弹作用随着唑来膦酸盐的治疗而减轻。然而,目前尚不清楚这种缓解在长期使用狄诺沙单抗治疗后是否足够。目的本回顾性观察性研究根据治疗时间和随后的唑来膦酸盐方案,分析了去诺沙单抗治疗后骨密度(BMD)和骨转换标志物(BTM)的变化。方法我们测量了282名绝经后骨质疏松症妇女的结果,这些妇女停用了替诺沙单抗并接受了唑来膦酸酯6 几个月后。在长期使用狄诺沙单抗治疗的患者中(≥5 年),BTM每3次测量 月,如果BTM水平增加≥2倍,则给予第二次唑来膦酸盐输注。所有女性的骨密度在denosumab治疗前、最后一次注射时和1至2次注射时进行测量 在第一个唑来膦酸酯之后的几年。结果10岁患者从替诺沙单抗转为唑来膦酸盐后的酮损失更高 ± 2次注射狄诺沙单抗(n = 84)相比之下为5 ± 2次注射(n = 144,p < 腰椎和股骨颈0.001),但随着治疗持续时间≥15,没有进一步增加 ± 2次注射(n = 54,p = 0.35和p = 0.20)。注射狄诺沙单抗≥10次的患者BTMs升高6 唑来膦酸盐治疗后数月,但并非全部。24名妇女接受了第二剂唑来膦酸盐6 第一个月后。这些患者的BTMs随后降低,但腰椎和髋关节的骨丢失与仅服用一剂唑来膦酸盐的患者相当(p = 腰椎0.37,p = 股骨颈0.97) 年,无论随后唑来膦酸盐治疗的频率如何。
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Effects of zoledronate on bone mineral density and bone turnover after long-term denosumab therapy: Observations in a real-world setting.
BACKGROUND The rebound effect after denosumab discontinuation is lessened with subsequent zoledronate therapy. However, it is unclear whether this mitigation is sufficient after long-term denosumab treatment. OBJECTIVE This retrospective observational study analysed bone mineral density (BMD) and bone turnover marker (BTM) changes after denosumab therapy according to treatment duration and subsequent zoledronate regimen. METHODS We measured the outcomes of 282 women with postmenopausal osteoporosis who discontinued denosumab and received zoledronate 6 months later. In patients with longer denosumab therapy (≥5 years), BTMs were measured every 3 months and a second zoledronate infusion was administered if BTM levels increased by ≥2-fold. The BMD of all women was measured before denosumab therapy, at the last injection and 1 to 2 years after the first zoledronate. RESULTS Bone loss after switching from denosumab to zoledronate was higher in patients with 10 ± 2 denosumab injections (n = 84) compared to 5 ± 2 injections (n = 144, p < 0.001 for lumbar spine and femoral neck), but there was no further increase with treatment durations of ≥15 ± 2 injections (n = 54, p = 0.35 and p = 0.20, respectively). BTMs in patients with ≥10 denosumab injections were elevated 6 months after zoledronate in some patients, but not all. Twenty-four women received a second zoledronate dose 6 months after the first one. BTMs in these patients were subsequently lower, but bone loss at both the lumbar spine and hip was comparable to that in patients with only one zoledronate dose (p = 0.37 for lumbar spine and p = 0.97 for femoral neck). CONCLUSIONS Rebound-associated bone loss reached a plateau after denosumab treatment durations of 4-6 years, irrespective of the frequency of subsequent zoledronate therapy.
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