Department of Endocrinology, National Health Commission Key Laboratory of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Department of Osteoporosis and Bone Disease, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Arch Osteoporos. 2022 Jul 28;17(1):103. doi: 10.1007/s11657-022-01131-8.
The efficacy of generic teriparatide in improving BMD at lumbar spine in patients with osteoporosis was similar to that of alendronate. It provided a new choice for osteoporosis treatment in Chinese population.
To determine whether the efficacy of generic teriparatide is noninferior to alendronate for Chinese postmenopausal women with osteoporosis.
Eligible patients were randomly assigned (2:1) in a 48-week, open-label design to receive 20 µg sc daily teriparatide or 70 mg oral weekly alendronate. Primary outcome was percentage change in BMD at the lumbar spine from baseline to 48 weeks and was assessed for non-inferiority. The same outcome was further assessed for superiority as a secondary endpoint.
Three hundred ninety-one and 196 participants were randomly assigned to the teriparatide or alendronate group, of whom 379 and 194 receiving at least one dose of teriparatide and alendronate treatment were eligible for the efficacy analysis. Teriparatide was non-inferior to alendronate for BMD change at lumbar spine (treatment difference: 0.7%, 95% CI: - 0.3 to 1.7%), which excluded the predefined non-inferiority margin of - 1.5%. However, teriparatide was not statistically superior to alendronate in improving BMD at lumbar spine (P = 0.169). At 48 weeks, changes in BMD at total hip were - 1.0% and 2.2% in teriparatide and alendronate group, respectively (P < 0.001). The incidence of new fracture showed no statistical difference between groups (P = 0.128). Serum P1NP and β-CTX levels significantly increased in the teriparatide group and markedly decreased in alendronate group (all P < 0.001 vs baseline). The adverse events (AEs) and serious AEs were more common in the teriparatide group than in the alendronate group, which were mainly teriparatide-related hypercalcemia, elevated alkaline phosphatase or parathyroid hormone, dizziness, and arthralgia.
Teriparatide was not inferior to alendronate in increasing BMD at lumbar spine in Chinese postmenopausal women, and they achieved these effects through different mechanisms.
确定国产特立帕肽治疗中国绝经后骨质疏松症患者的疗效是否不劣于阿仑膦酸钠。
符合条件的患者按 2∶1 随机分配(48 周、开放性设计),接受每日皮下注射 20μg 特立帕肽或每周口服 70mg 阿仑膦酸钠治疗。主要结局为腰椎骨密度从基线到 48 周的变化百分比,评估非劣效性。同一结局作为次要终点进一步评估优效性。
391 名和 196 名参与者被随机分配至特立帕肽或阿仑膦酸钠组,其中 379 名和 194 名至少接受一剂特立帕肽和阿仑膦酸钠治疗的参与者符合疗效分析的条件。特立帕肽在腰椎骨密度变化方面不劣于阿仑膦酸钠(治疗差异:0.7%,95%CI:-0.3 至 1.7%),排除了预先设定的-1.5%非劣效性边界。然而,特立帕肽在改善腰椎骨密度方面并未显著优于阿仑膦酸钠(P=0.169)。48 周时,特立帕肽组和阿仑膦酸钠组全髋骨密度变化分别为-1.0%和 2.2%(P<0.001)。两组新发骨折发生率无统计学差异(P=0.128)。特立帕肽组血清 P1NP 和β-CTX 水平显著升高,阿仑膦酸钠组显著降低(均 P<0.001 与基线相比)。特立帕肽组不良事件(AE)和严重 AE 较阿仑膦酸钠组更为常见,主要为特立帕肽相关高钙血症、碱性磷酸酶或甲状旁腺激素升高、头晕和关节痛。
国产特立帕肽在增加中国绝经后妇女腰椎骨密度方面不劣于阿仑膦酸钠,且两者通过不同机制达到这一效果。