Ganda K, Seibel M J
Department of Endocrinology and Metabolism, Concord Hospital, Level 6 Concord Hospital Medical Centre, Hospital Road, Concord, NSW, 2139, Australia,
Osteoporos Int. 2014 Feb;25(2):777-82. doi: 10.1007/s00198-013-2585-1. Epub 2013 Dec 6.
We report on the clinical and biochemical outcomes in two adult patients with active polyostotic fibrous dysplasia (FD) treated with the RANK-L inhibitor, denosumab, following unsatisfactory responses to prior long-term bisphosphonate therapy. A 44-year-old female (case 1) who had received a cumulative dose of 20 mg zoledronic acid over 2.5 years and a 48-year-old male (case 2) who had received a cumulative dose of 45 mg zoledronic acid over 8 years both experienced minimal reductions in pain scores and markers of bone turnover. Following initiation of denosumab 60 mg sc, changes in bone pain, bone turnover [assessed by serum amino-terminal propeptide of type I collagen (PINP) and urinary deoxypyridinoline] were monitored over a period of 20 and 8 months, respectively. Following administration of denosumab, both patients demonstrated a rapid and pronounced biochemical response: Within 4-7 weeks, bone turnover markers fell to levels within the respective reference range, and one patient reported a reduction in pain. Treatment with denosumab was well tolerated. However, transient asymptomatic hypocalcaemia and/or hypophosphatemia associated with a transient two to threefold increase in serum PTH levels was observed in both patients. Dosing intervals for denosumab varied significantly between the two patients, depending on disease activity at baseline. Denosumab appears to be effective in reducing bone turnover in adult patients with active FD. However, caution should be exercised, and patients should be monitored carefully as significant fluctuations in biochemical and hormonal indices can occur.
我们报告了两名患有活动性多骨型纤维发育不良(FD)的成年患者在接受RANK-L抑制剂地诺单抗治疗后的临床和生化结果,这两名患者之前长期接受双膦酸盐治疗效果不佳。一名44岁女性(病例1)在2.5年期间累计接受了20mg唑来膦酸治疗,一名48岁男性(病例2)在8年期间累计接受了45mg唑来膦酸治疗,两人的疼痛评分和骨转换标志物均仅有极小幅度降低。在开始皮下注射60mg地诺单抗后,分别在20个月和8个月的时间内监测骨痛、骨转换[通过血清I型胶原氨基端前肽(PINP)和尿脱氧吡啶啉评估]的变化。给予地诺单抗后,两名患者均表现出快速且显著的生化反应:在4 - 7周内,骨转换标志物降至各自参考范围内,一名患者报告疼痛减轻。地诺单抗治疗耐受性良好。然而,两名患者均观察到与血清甲状旁腺激素水平短暂升高2至3倍相关的短暂无症状性低钙血症和/或低磷血症。两名患者的地诺单抗给药间隔差异显著,取决于基线时的疾病活动情况。地诺单抗似乎对降低活动性FD成年患者的骨转换有效。然而,应谨慎行事,并且由于生化和激素指标可能出现显著波动,应对患者进行仔细监测。