School of Clinical Medicine, Weifang Medical University, Affiliated Hospital of Weifang Medical University, Weifang, Shandong Province, China.
Department of Endocrinology and Metabolic Diseases, Affiliated Hospital of Weifang Medical University, Weifang, Shandong Province, China.
Medicine (Baltimore). 2023 Nov 10;102(45):e35946. doi: 10.1097/MD.0000000000035946.
With the popularity of ICIs in different oncology treatments, immune-related adverse events have raised concerns, mostly occurring in skin and endocrine gland injury. This disease involves different organ systems and presents with a variety of clinical manifestations. Most patients with immune checkpoint inhibitor-induced type 1 diabetes are reported to have no combination of autoimmune disease. We report a case of Sintilimab-related diabetes mellitus and psoriasis.
We report a case of a 65-year-old female with Sintilimab-related diabetes mellitus and psoriasis.
The patient treated with anti-programmed cell death protein 1 (Sintilimab) for 4 cycles. The patient presented with inexplicable bouts of nausea and vomiting, accompanied by chest discomfort and a feeling of breathlessness, prompting their admission to the local hospital. The initial assessment upon admission revealed an abrupt elevation in blood glucose levels, alongside normal ketone levels, lactic acidosis, and hyperuricemia. A comprehensive regimen was provided to regulate glucose levels and address the symptoms, resulting in notable improvement and subsequent discharge. Regrettably, the patient's personal decision to discontinue medication for a single day led to the emergence of acute ketoacidosis, coupled with a recurrence of psoriasis vulgaris. Consequently, readmission became necessary. Based on the patient's medical history and diabetes antibody testing, the diagnosis of immune checkpoint inhibitor induced diabetes mellitus has been confidently established.
The patient ceased treatment with Sintilimab and was initiated on insulin therapy for glycemic control, alongside symptomatic management for psoriasis. Upon stabilization of the condition, long-term administration of exogenous insulin was implemented as a substitute treatment.
Outside of the hospital, insulin therapy effectively maintained stable blood glucose levels, and there were no further episodes of psoriasis flare-ups.
The clinical manifestations of immune checkpoint inhibitor induced diabetes mellitus are variable, and in this case the patient presented with unique primary symptoms. Therefore, it is crucial to accumulate relevant cases, understand the different clinical presentations and identify the underlying mechanisms of the disease. This will provide further evidence for early therapeutic intervention in similar patients in the future.
随着免疫检查点抑制剂在不同肿瘤治疗中的普及,免疫相关不良反应引起了关注,主要发生在皮肤和内分泌腺损伤。这种疾病涉及不同的器官系统,表现出多种临床表现。大多数免疫检查点抑制剂诱导的 1 型糖尿病患者报告没有自身免疫性疾病的合并症。我们报告了一例信迪利单抗相关的糖尿病和银屑病。
我们报告了一例 65 岁女性患者,因信迪利单抗相关糖尿病和银屑病就诊。
患者接受了 4 个周期的抗程序性死亡蛋白 1(信迪利单抗)治疗。患者出现不明原因的恶心和呕吐,伴有胸痛和呼吸困难,因此入住当地医院。入院时的初步评估显示血糖水平突然升高,同时酮体水平正常,无酸中毒,尿酸升高。给予全面的治疗方案来调节血糖水平并缓解症状,病情明显改善后出院。遗憾的是,由于患者个人决定停药一天,导致急性酮症酸中毒,同时寻常型银屑病复发。因此需要再次住院。根据患者的病史和糖尿病抗体检测结果,确诊为免疫检查点抑制剂诱导的糖尿病。
患者停止使用信迪利单抗,并开始胰岛素治疗以控制血糖,同时对症治疗银屑病。病情稳定后,长期给予外源性胰岛素替代治疗。
患者出院后,胰岛素治疗有效维持了血糖稳定,银屑病无再发。
免疫检查点抑制剂诱导的糖尿病的临床表现多种多样,本例患者表现出独特的首发症状。因此,积累相关病例、了解不同的临床表现和识别疾病的潜在机制至关重要。这将为未来类似患者的早期治疗干预提供更多证据。