Saito Yoshitaka, Uchiyama Kazuki, Sakamoto Tatsuhiko, Yamazaki Kojiro, Kubota Kosei, Takekuma Yoh, Komatsu Yoshito, Sugawara Mitsuru
Department of Pharmacy, Hokkaido University Hospital.
Cancer Center, Hokkaido University Hospital.
Yakugaku Zasshi. 2021;141(8):1023-1030. doi: 10.1248/yakushi.21-00055.
Denosumab is a fully monoclonal antibody against the receptor activator of nuclear factor kappa-B ligand (RANKL), and prevents skeletal-related events by bone metastasis. Hypocalcemia is the most typical adverse effect of denosumab use. We have developed a management system for the more efficient and safer management of denosumab administration, and evaluated pharmaceutical interventions for the better control of hypocalcemia. All pharmaceutical interventions in the system from April 2016 to March 2020 were retrospectively evaluated. We have also assessed the incidence of hypocalcemia in 158 patients who were administered denosumab for six months or more in the period. A total of 282 pharmaceutical interventions (7.0% of the total administration) were conducted. The most conducted intervention was regarding hypocalcemia, which involved the suspension of the injection and/or the increase of calcium and vitamin D supplement with 65% adoption and 17% temporary treatment suspensions. Other interventions were about hypercalcemia, request of laboratory examination and ordering supplements, dental consultation, and poor renal function. A total of 199 interventions (70.6%) were adopted, with 33 administrations suspended. The frequency of hypocalcemia was 27.8% with just one patient having grade 2 hypocalcemia, suggesting that there were no severe cases. Moreover, hypocalcemia was significantly normalized following pharmaceutical intervention and/or handling by physicians (p=0.02) according to the system. Conversely, the normalization rate in hypercalcemia did not differ according to the countermeasures. In conclusion, pharmaceutical interventions according to our management system benefit safe denosumab treatment, especially in severe hypocalcemia prevention.
地诺单抗是一种完全针对核因子κB受体活化因子配体(RANKL)的单克隆抗体,可预防骨转移引起的骨骼相关事件。低钙血症是使用地诺单抗最典型的不良反应。我们开发了一种管理系统,用于更高效、安全地管理地诺单抗给药,并评估了药物干预措施以更好地控制低钙血症。对2016年4月至2020年3月该系统中的所有药物干预措施进行了回顾性评估。我们还评估了在此期间接受地诺单抗治疗6个月或更长时间的158例患者的低钙血症发生率。共进行了282次药物干预(占总给药次数的7.0%)。最常进行的干预是针对低钙血症,包括暂停注射和/或增加钙和维生素D补充剂,采用率为65%,临时治疗暂停率为17%。其他干预涉及高钙血症、实验室检查请求和补充剂订购、牙科咨询以及肾功能不佳。共采用了199次干预(70.6%),33次给药暂停。低钙血症发生率为27.8%,仅有1例患者为2级低钙血症,表明无严重病例。此外,根据该系统,药物干预和/或医生处理后低钙血症显著恢复正常(p=0.02)。相反,高钙血症的恢复率根据对策不同而无差异。总之,根据我们的管理系统进行药物干预有利于地诺单抗的安全治疗,尤其是在预防严重低钙血症方面。