Department of Orthopaedic Surgery, Showa University School of Medicine, Tokyo, Japan,
Department of Orthopaedic and Spine Surgery, Sanraku Hospital, Tokyo, Japan,
Clin Interv Aging. 2018 Oct 8;13:1929-1934. doi: 10.2147/CIA.S180614. eCollection 2018.
Denosumab is a fully human monoclonal antibody against the receptor activator of nuclear factor-κB ligand (RANKL) that is used for the treatment of osteoporosis. Denosumab-induced hypocalcemia is a rare but important adverse event, which is usually asymptomatic in patients with osteoporosis. It is also known that hypocalcemia is common in patients with bone metastases and severe renal impairment. Here we report a case of symptomatic hypocalcemia following administration of 60 mg of denosumab in a patient with high bone turnover and no renal impairment (estimated glomerular filtration rate [eGFR], 71 mL/min), despite prophylactic oral vitamin D administration. This report supports our observation that there is a risk of protracted and marked denosumab-induced hypocalcemia in patients with high bone turnover, irrespective of their degree of renal impairment.
地舒单抗是一种针对核因子-κB 配体受体激活剂(RANKL)的全人源单克隆抗体,用于治疗骨质疏松症。地舒单抗引起的低钙血症是一种罕见但重要的不良事件,在骨质疏松症患者中通常无症状。已知低钙血症在骨转移和严重肾功能不全的患者中很常见。在此,我们报告了一例在高骨转换且无肾功能不全(估算肾小球滤过率[eGFR]为 71 mL/min)的患者中,尽管预防性口服维生素 D 给药,但在使用 60 mg 地舒单抗后出现症状性低钙血症的病例。该报告支持我们的观察,即高骨转换的患者存在地舒单抗诱导的低钙血症持续时间长且严重的风险,而与肾功能不全的程度无关。