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罗莫佐单抗治疗绝经后骨质疏松症合并轻中度慢性肾脏病女性患者的疗效和安全性。

Efficacy and Safety of Romosozumab Among Postmenopausal Women With Osteoporosis and Mild-to-Moderate Chronic Kidney Disease.

机构信息

Colorado Center for Bone Health, Lakewood, CO, USA.

St. Joseph's Healthcare Hamilton, McMaster University, Hamilton, Canada.

出版信息

J Bone Miner Res. 2022 Aug;37(8):1437-1445. doi: 10.1002/jbmr.4563. Epub 2022 May 20.

Abstract

Patients with osteoporosis and chronic kidney disease (CKD) are at increased risk of fracture and associated negative outcomes, including increased mortality. The present post hoc analysis of two randomized, multicenter, phase 3 clinical trials-Fracture Study in Postmenopausal Women with Osteoporosis (FRAME) and Active-Controlled Fracture Study in Postmenopausal Women with Osteoporosis at High Risk (ARCH)-investigated the efficacy and safety of romosozumab in postmenopausal women with osteoporosis and mild-to-moderate CKD. The analysis included data from 7147 patients from FRAME and 4077 from ARCH. Eighty-one percent of patients from FRAME and 85% from ARCH had mild or moderate reduction in estimated glomerular filtration rate (eGFR) at baseline, and part of this reduction is likely age related. During the 1-year double-blind phases of the trials, patients received romosozumab 210 mg sc or placebo monthly in FRAME and romosozumab 210 mg sc monthly or alendronate 70 mg po weekly in ARCH. Bone mineral density (BMD) at the lumbar spine, total hip, and femoral neck and vertebral and nonvertebral fractures were assessed at baseline and month 12. In both trials, the least-square mean percent change from baseline BMD was significantly greater in the romosozumab groups versus controls across all kidney function categories at month 12. Romosozumab reduced the relative risk of new vertebral fractures at month 12 among patients with eGFR of 30-59, 60-89, and ≥90 mL/min by 72% (95% confidence interval [CI] 14-91; p = 0.017), 70% (40-85; p < 0.001), and 84% (30-96; p = 0.005), respectively, in FRAME versus placebo, and by 51% (5-75; p = 0.04), 19% (-28 to 49; p = 0.39), and 57% (1-81, p = 0.04), respectively, in ARCH versus alendronate. Incidences of adverse events, asymptomatic decreases in serum calcium, and evolution of kidney function during the studies were similar across all baseline kidney function groups. Romosozumab is an effective treatment option for postmenopausal women with osteoporosis and mild-to-moderate reduction in kidney function, with a similar safety profile across different levels of kidney function. © 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

摘要

患者患有骨质疏松症和慢性肾脏病 (CKD) 时,骨折风险及相关不良结局(包括死亡率增加)的风险会增加。本研究是对两项随机、多中心、3 期临床试验(绝经后妇女骨质疏松症骨折研究 [FRAME] 和绝经后高风险骨质疏松症妇女的活性对照骨折研究 [ARCH])的事后分析,研究了罗莫佐单抗在骨质疏松症和轻度至中度 CKD 绝经后妇女中的疗效和安全性。该分析纳入了 FRAME 研究的 7147 例患者和 ARCH 研究的 4077 例患者的数据。FRAME 研究中 81%的患者和 ARCH 研究中 85%的患者在基线时有轻度或中度估计肾小球滤过率(eGFR)下降,部分下降可能与年龄有关。在两项试验的 1 年双盲阶段,患者每月接受 FRAME 中的罗莫佐单抗 210mg sc 或安慰剂,以及 ARCH 中的罗莫佐单抗 210mg sc 或阿仑膦酸钠 70mg po。在基线和第 12 个月评估腰椎、全髋和股骨颈以及椎体和非椎体骨折的骨密度 (BMD)。在两项试验中,与对照组相比,所有肾功能类别中,罗莫佐单抗组在第 12 个月时腰椎、全髋和股骨颈的骨密度较基线的最小平方均数百分比变化在罗莫佐umab 组中更为显著。与 FRAME 中的安慰剂相比,eGFR 为 30-59、60-89 和≥90mL/min 的患者在第 12 个月时新椎体骨折的相对风险分别降低了 72%(95%置信区间[CI] 14-91;p=0.017)、70%(40-85;p<0.001)和 84%(30-96;p=0.005),与 ARCH 中的阿仑膦酸钠相比,分别降低了 51%(5-75;p=0.04)、19%(-28 至 49;p=0.39)和 57%(1-81,p=0.04)。在所有基线肾功能组中,不良事件的发生率、血清钙的无症状下降以及研究期间肾功能的变化相似。罗莫佐单抗是一种有效的治疗选择,适用于患有骨质疏松症和轻度至中度肾功能下降的绝经后妇女,在不同肾功能水平下具有相似的安全性。

© 2022 作者。《骨矿盐研究杂志》由 Wiley 期刊出版公司代表美国骨矿盐研究协会(ASBMR)出版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b7/9544335/83592c0437dc/JBMR-37-1437-g001.jpg

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