Division of Endocrinology, Department of Internal Medicine, Endocrine Research Institute, Yonsei University College of Medicine, Seoul, 03722, Republic of Korea.
Division of Endocrinology, Department of Internal Medicine, National Health Insurance Service Ilsan Hospital, Goyang, 10444, Korea.
Osteoporos Int. 2023 Dec;34(12):2059-2067. doi: 10.1007/s00198-023-06889-2. Epub 2023 Aug 19.
In this study, romosozumab demonstrated significantly greater improvement in trabecular bone score compared to denosumab therapy in postmenopausal women previously treated with antiresorptive agents. Notably, in patients previously treated with anti-resorptive agents, treatment with romosozumab resulted in similar increases in trabecular bone score compared to that of drug-naïve patients.
Romosozumab significantly increases bone mineral density (BMD) and rapidly reduces fracture risk. Whether romosozumab can improve the spinal trabecular bone score (TBS) as a bone quality indicator merits further investigation.
Data for postmenopausal women starting romosozumab or denosumab treatment at Severance Hospital, Korea, were analyzed. Romosozumab and denosumab groups were 1:1 matched using propensity scores, considering relevant covariates. Good responders were defined as those with TBS improvement of 5.8% or greater.
Overall, 174 patients (romosozumab, n = 87; denosumab, n = 87) were analyzed. Matched groups did not differ in age (64 years), weight, height, previous fracture (38%), lumbar spine or femoral neck BMD (T-score, -3.4 and -2.6, respectively), or prior bisphosphonate or selective estrogen receptor modulator (SERM) exposure (50%). The romosozumab group exhibited a greater increase in lumbar spine BMD (15.2% vs. 6.9%, p < 0.001) and TBS (3.7% vs. 1.7%, p = 0.013) than the denosumab group. In patients transitioning from bisphosphonate or SERM, romosozumab users showed greater improvement in TBS compared to denosumab users (3.9% versus 0.8%, P = 0.006); the drug-naive group showed no significant difference (3.6% versus 2.7%, P = 0.472). The romosozumab group had a higher proportion of good responders than the denosumab group (33.3% vs. 18.4%, p = 0.024). Romosozumab therapy for 12 months resulted in 3.8-fold higher odds of a good response in TBS than denosumab after covariate adjustment (adjusted odds ratio 3.85, p = 0.002).
Romosozumab could improve bone mass and bone quality, measured by TBS, in postmenopausal osteoporosis, particularly as a subsequent regimen in patients previously taking anti-resorptive agents.
罗莫佐单抗可显著增加骨密度(BMD)并迅速降低骨折风险。罗莫佐单抗是否能改善作为骨质量指标的脊柱小梁骨评分(TBS)值得进一步研究。
分析了韩国首尔峨山医院开始使用罗莫佐单抗或地舒单抗治疗的绝经后妇女的数据。使用倾向评分,考虑相关协变量,将罗莫佐单抗组和地舒单抗组以 1:1 匹配。将 TBS 改善 5.8%或以上的患者定义为治疗有效者。
共分析了 174 名患者(罗莫佐单抗组 87 例,地舒单抗组 87 例)。匹配组在年龄(64 岁)、体重、身高、既往骨折(38%)、腰椎或股骨颈 BMD(T 评分,分别为-3.4 和-2.6)或既往双膦酸盐或选择性雌激素受体调节剂(SERM)暴露(50%)方面无差异。与地舒单抗组相比,罗莫佐单抗组腰椎 BMD 增加(15.2%对 6.9%,p<0.001)和 TBS 增加(3.7%对 1.7%,p=0.013)更明显。在从双膦酸盐或 SERM 转换的患者中,与地舒单抗组相比,罗莫佐单抗组的 TBS 改善更明显(3.9%对 0.8%,p=0.006);而在未用药组中,两组之间没有显著差异(3.6%对 2.7%,p=0.472)。与地舒单抗组相比,罗莫佐单抗组的治疗有效者比例更高(33.3%对 18.4%,p=0.024)。调整协变量后,罗莫佐单抗治疗 12 个月后 TBS 治疗有效的可能性是地舒单抗的 3.8 倍(调整后的优势比 3.85,p=0.002)。
罗莫佐单抗可改善绝经后骨质疏松症的骨量和骨质量,用 TBS 测量,尤其是在既往使用抗吸收剂的患者中作为后续治疗方案。