CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Diabetic ketoacidosis induced by nivolumab in invasive mucinous adenocarcinoma of the lung: a case report and review of the literature.
Diabetic ketoacidosis induced by nivolumab in invasive mucinous adenocarcinoma of the lung: a case report and review of the literature.
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nivolumab 诱发的糖尿病酮症酸中毒潜伏期分散,临床风险高。患者需终身胰岛素治疗。在 nivolumab 免疫治疗前及治疗期间应常规监测血糖和 HbA1c,以避免糖尿病酮症酸中毒的发生。糖尿病酮症酸中毒发生后,应使用胰岛素积极控制血糖,并做好用药教育,确保患者长期依从性。只有在血糖稳定控制下患者具有临床获益时,才可启动 nivolumab。
纳武利尤单抗是中国首个获批的programmed cell death receptor 1(PD-1)抑制剂。与化疗相比,纳武利尤单抗在多种肿瘤治疗中显示出疗效好、安全性高的优势。然而,由于其在中国使用时间短、缺乏安全性经验,临床对其不良反应的认识尚未充分阐明。近年来,急诊科报道了由纳武利尤单抗引起的糖尿病酮症酸中毒病例,引起了我们的关注。病例描述:本文报告一例69岁女性肺浸润性黏液腺癌患者,在接受PD-1抑制剂纳武利尤单抗及树突状细胞/细胞因子诱导的杀伤细胞(DC/CIK)免疫治疗后发生严重糖尿病酮症酸中毒。她在第二周期纳武利尤单抗给药后5天出现糖尿病酮症酸中毒。患者表现为口干症状,最高血糖为511.2 mg/dL,血红蛋白A1c(HbA1c)水平为7.4%,尿酮体值为3+,细胞外液剩余碱水平为-3.8 mmol/L。开始给予生理盐水和胰岛素治疗。患者无肥胖史或糖尿病家族史。在此期间她接受了一次3.75 mg地塞米松治疗,咳嗽有所改善,但不能解释糖尿病的发生。她接受了胰岛素、磷酸西格列汀片和阿卡波糖片治疗。糖尿病酮症酸中毒被认为是纳武利尤单抗引起的免疫相关毒性,因此暂停了纳武利尤单抗治疗。患者在胰岛素治疗下维持,血糖水平恢复正常。
Nivolumab is the first programmed cell death receptor 1 (PD-1) inhibitor approved in China. Compared with chemotherapy, nivolumab has shown advantages of good efficacy and safety in the treatment of a variety of tumors. However, due to its short time of use in China and lack of safety experience, clinical understanding of its adverse reactions has not been sufficiently elucidated. In recent years, cases of diabetic ketoacidosis caused by nivolumab have been reported in the emergency department, which has aroused our concern. CASE DESCRIPTION: Here we present a serious case of diabetic ketoacidosis in a 69-year-old woman with invasive mucinous adenocarcinoma of the lung, which occurred following therapy with the PD-1 inhibitor nivolumab and dendritic cell/cytokine-induced killer cell (DC/CIK) immunotherapy. She presented with diabetic ketoacidosis 5 days after the second cycle of nivolumab administration. The patient presented with dry mouth symptoms, a maximum blood glucose of 511.2 mg/dL, hemoglobin A1c (HbA1c) level of 7.4%, urine ketone body value of 3+, and extracellular fluid residual alkali level of -3.8 mmol/L. Normal saline and insulin was initiated. The patient had no history of obesity or family history of diabetes. She received a single dose of 3.75 mg of dexamethasone treatment during this period of time which resulted in cough improvement, but did not explain the onset of the diabetes. She was treated with insulin, sitagliptin phosphate tablets and acarbose tablets. Diabetic ketoacidosis was considered an immune-related toxicity caused by nivolumab, and consequently, treatment with nivolumab was suspended. Patient was maintained under insulin treatment with a blood glucose levels normalization.
The incubation period of nivolumab-induced diabetic ketoacidosis is dispersive and the clinical risk is high. Patients need life-long insulin therapy. Blood glucose and HbA1c should be monitored routinely before and during nivolumab immunotherapy to avoid the occurrence of diabetic ketoacidosis. After the occurrence of diabetic ketoacidosis, insulin should be used to actively control blood glucose and do a good job in medication education to ensure long-term compliance of patients. Nivolumab should only be initiated if the patient has a clinical benefit under stable glucose control.
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