Division of Endocrinology, Diabetes and Metabolism, Centro Hospitalar Universitário de Santo António, Oporto, Portugal.
Division of Internal Medicine, Centro Hospitalar Universitário de Santo António, Oporto, Portugal.
J Oncol Pharm Pract. 2024 Sep;30(6):1118-1121. doi: 10.1177/10781552241255699. Epub 2024 May 20.
Immunotherapy has a crucial role in the current treatment of multiple malignancies. Albeit described as rare, new onset autoimmune diabetes is a potentially life-threatening complication of programmed cell death-1 (PD-1) inhibitors, such as pembrolizumab, and its predisposing factors and pathological mechanism are yet to be clarified.
We present a case of a 72-year-old man with a high-grade bladder carcinoma undergoing pembrolizumab treatment. He had no personal or family history of diabetes mellitus but was diagnosed with primary hypothyroidism four months after starting pembrolizumab. Two years after starting pembrolizumab, he presented in the emergency department due to abdominal pain, anorexia, polydipsia, polyuria and vomiting over the preceding five days and he met criteria for severe diabetic ketoacidosis (DKA). Three days prior to his admission, he had received prednisolone therapy for suspected hypersensitivity related to a contrast-enhanced imaging that he performed.
MANAGEMENT & OUTCOME: Prompt treatment for DKA was started, with transition to insulin basal-bolus therapy after DKA resolution, with progressive glycaemic stabilization. Further investigation revealed low C-peptide levels (0.07 ng/dL, with a fasting blood glucose of 288 mg/dL), HbA1c 9.2% and positive anti-IA2 antibodies, which allowed the diagnosis of new-onset autoimmune diabetes. Pembrolizumab was transiently suspended, and the patient resumed treatment after glycaemic profile optimization under multiple daily insulin administrations two months later.
This case highlights the importance of clinical suspicion and glycaemic monitoring as an integral part of treatment protocols in patients on pembrolizumab and other immune checkpoint inhibitors. Additional research and investigation into the underlying mechanisms of this condition are necessary to identify potential screening tests for individuals at higher risk of developing DM and to guide the implementation of management and preventive strategies for ketoacidosis complication.
免疫疗法在当前多种恶性肿瘤的治疗中具有重要作用。程序性细胞死亡-1(PD-1)抑制剂,如派姆单抗,尽管被描述为罕见,但新出现的自身免疫性糖尿病是一种潜在危及生命的并发症,其易患因素和病理机制尚不清楚。
我们报告了一例 72 岁男性患有高级别膀胱癌,正在接受派姆单抗治疗。他没有糖尿病个人或家族史,但在开始派姆单抗治疗四个月后被诊断为原发性甲状腺功能减退症。开始派姆单抗治疗两年后,他因腹痛、食欲不振、多饮、多尿和呕吐五天前到急诊就诊,符合严重糖尿病酮症酸中毒(DKA)的标准。在他入院前三天,他因怀疑与他进行的增强成像相关的过敏而接受了泼尼松龙治疗。
迅速开始治疗 DKA,并在 DKA 缓解后过渡到胰岛素基础-餐时治疗,血糖逐渐稳定。进一步的调查显示 C 肽水平低(0.07ng/dL,空腹血糖为 288mg/dL),HbA1c 为 9.2%,抗 IA2 抗体阳性,这允许诊断为新发自身免疫性糖尿病。暂时暂停派姆单抗治疗,两个月后血糖谱优化后在多次胰岛素皮下注射下恢复治疗。
本病例强调了在接受派姆单抗和其他免疫检查点抑制剂治疗的患者中,临床怀疑和血糖监测作为治疗方案不可或缺的一部分的重要性。需要进一步研究和调查这种情况的潜在机制,以确定易患糖尿病的个体的潜在筛查测试,并指导酮症酸中毒并发症的管理和预防策略的实施。