Department of Pharmacy, Tokushima University Hospital.
Biol Pharm Bull. 2013;36(10):1622-6. doi: 10.1248/bpb.b13-00496. Epub 2013 Aug 9.
Denosumab, a fully human monoclonal antibody that inhibits the receptor activator of nuclear factor-κB ligand, inhibits the activation of osteoclasts. Some clinical trials have shown that denosumab suppresses bone resorption in patients with advanced cancer, but hypocalcemia has been reported as a serious adverse effect after the administration of denosumab. It is difficult to predict hypocalcemia in such cases because the risk factors for denosumab-induced hypocalcemia have not been reported. Accordingly, the aim of the present study was to identify the risk factors for hypocalcemia induced by denosumab. We retrospectively reviewed the records of patients who had received denosumab at Tokushima University Hospital between April 2012 and May 2013. Fifty-three patients were analyzed and eleven patients had hypocalcemia after administration of denosumab. Univariate logistic regression analysis revealed that the patients who had not been administered zoledronic acid before receiving denosumab or had lower creatinine clearance (CCr) appeared to have a higher risk of hypocalcemia (p<0.05). The cut off value of CCr was 50.4 mL/min calculated by receiver-operator characteristics curves. Moreover, multivariate logistic regression analysis revealed that non-administration of zoledronic acid (odds ratio 10.43, p<0.05) and CCr less than 50.0 mL/min (odds ratio 5.90, p<0.05) were independent risk factors for denosumab-induced hypocalcemia. These findings provide useful information regarding the monitoring of hypocalcemia in patients receiving denosumab.
地舒单抗是一种完全人源化单克隆抗体,能抑制核因子-κB 配体受体激活剂,从而抑制破骨细胞的激活。一些临床试验表明,地舒单抗能抑制晚期癌症患者的骨吸收,但有报道称地舒单抗给药后会出现严重的低钙血症不良反应。由于尚未报道地舒单抗诱导性低钙血症的危险因素,因此难以预测此类情况下的低钙血症。因此,本研究旨在确定地舒单抗诱导低钙血症的危险因素。我们回顾性分析了 2012 年 4 月至 2013 年 5 月在徳岛大学医院接受地舒单抗治疗的患者的记录。对 53 例患者进行了分析,其中 11 例患者在接受地舒单抗治疗后出现低钙血症。单因素 logistic 回归分析显示,在接受地舒单抗治疗前未接受唑来膦酸治疗或肌酐清除率(CCr)较低的患者似乎有更高的低钙血症风险(p<0.05)。CCr 的截断值通过受试者工作特征曲线计算为 50.4 mL/min。此外,多因素 logistic 回归分析显示,未使用唑来膦酸(比值比 10.43,p<0.05)和 CCr 低于 50.0 mL/min(比值比 5.90,p<0.05)是地舒单抗诱导性低钙血症的独立危险因素。这些发现为监测接受地舒单抗治疗的患者低钙血症提供了有用的信息。