Kusuki Kazuhisa, Suzuki Saya, Mizuno Yuzo
Department of Diabetes and Endocrinology, Kanto Central Hospital of the Mutual Aid Association of Public School Teachers, Setagaya-ku, Tokyo, Japan.
Endocrinol Diabetes Metab Case Rep. 2020 Apr 29;2020. doi: 10.1530/EDM-19-0152.
A 72-year-old man with no history of diabetes was referred to our department due to hyperglycemia during pembrolizumab treatment for non-small-cell lung carcinoma. His blood glucose level was 209 mg/dL, but he was not in a state of ketosis or ketoacidosis. Serum C-peptide levels persisted at first, but gradually decreased, and 18 days later, he was admitted to our hospital with diabetic ketoacidosis (DKA). The patient was diagnosed with fulminant type 1 diabetes (FT1D) induced by pembrolizumab. According to the literature, the insulin secretion capacity of a patient with type 1 diabetes (T1D) induced by anti-programmed cell death-1 (anti-PD-1) antibody is depleted in approximately 2 to 3 weeks, which is longer than that of typical FT1D. Patients with hyperglycemia and C-peptide persistence should be considered for hospitalization or frequent outpatient visits with insulin treatment because these could indicate the onset of life-threatening FT1D induced by anti-PD-1 antibodies. Based on the clinical course of this patient and the literature, we suggest monitoring anti-PD-1 antibody-related T1D.
Immune checkpoint inhibitors, such as anti-PD-1 antibodies, are increasingly used as anticancer drugs. Anti-PD-1 antibodies can cause immune-related adverse events, including T1D. FT1D, a novel subtype of T1D, is characterized by the abrupt onset of hyperglycemia with ketoacidosis, a relatively low glycated hemoglobin level and depletion of C-peptide level at onset. In patients being treated with anti-PD-1 antibody, hyperglycemia with C-peptide level persistence should be monitored through regular blood tests. Because of C-peptide persistence and mild hyperglycemia, it is possible to miss a diagnosis of life-threatening FT1D induced by anti-PD-1 antibody. In particular, in patients who have no history of diabetes, hyperglycemia without DKA is likely to be the very beginning of anti-PD-1 antibody-induced T1D. Therefore, such patients must be considered for either hospitalization or frequent outpatient visits with insulin injections and self-monitoring of blood glucose.
一名72岁无糖尿病病史的男性在接受派姆单抗治疗非小细胞肺癌期间因高血糖被转诊至我科。他的血糖水平为209mg/dL,但未处于酮症或酮症酸中毒状态。血清C肽水平起初持续存在,但逐渐下降,18天后,他因糖尿病酮症酸中毒(DKA)入院。该患者被诊断为派姆单抗诱导的暴发性1型糖尿病(FT1D)。根据文献,抗程序性细胞死亡蛋白1(抗PD-1)抗体诱导的1型糖尿病(T1D)患者的胰岛素分泌能力在约2至3周内耗尽,这比典型的FT1D时间更长。对于高血糖且C肽持续存在的患者,应考虑住院或频繁门诊就诊并进行胰岛素治疗,因为这些可能预示着抗PD-1抗体诱导的危及生命的FT1D的发作。基于该患者的临床病程及文献,我们建议监测抗PD-1抗体相关的T1D。
免疫检查点抑制剂,如抗PD-1抗体,越来越多地被用作抗癌药物。抗PD-1抗体可引起免疫相关不良事件,包括T1D。FT1D是T1D的一种新型亚型,其特征为高血糖伴酮症酸中毒突然发作、糖化血红蛋白水平相对较低以及发病时C肽水平降低。在接受抗PD-1抗体治疗的患者中,应通过定期血液检查监测高血糖伴C肽水平持续的情况。由于C肽持续存在且血糖轻度升高,可能会漏诊抗PD-1抗体诱导的危及生命的FT1D。特别是对于无糖尿病病史的患者,无DKA的高血糖很可能是抗PD-1抗体诱导的T1D的最初表现。因此,必须考虑让这类患者住院或频繁门诊就诊,进行胰岛素注射及血糖自我监测。