Kirksville College of Osteopathic Medicine, A.T. Still University, Kirksville, USA.
Internal Medicine Residency Program, University of Arizona College of Medicine - Phoenix, Phoenix, USA.
Cancer Rep (Hoboken). 2024 Nov;7(11):e70058. doi: 10.1002/cnr2.70058.
Immune checkpoint inhibitors (ICIs) are becoming more frequently used in the treatment of many types of malignant cancers by disinhibiting T-cell activation, which promotes the destruction of cancer cells. This disinhibition can also result in autoimmune conditions, like endocrinopathies.
We report a case of a 78-year-old male patient with malignant mesothelioma treated with combination ICI therapy who presented with diabetic ketoacidosis (DKA) with no history of diabetes mellitus or hyperglycemia. The patient was admitted to the intensive care unit and treated with intravenous (IV) fluid repletion and IV insulin for DKA. The patient was diagnosed with new-onset type 1 diabetes mellitus (T1DM) induced by ICI therapy.
Approximately 75% of patients diagnosed with ICI-induced T1DM initially present with DKA. This, along with the rapid onset of hyperglycemia in this patient, suggests current guidelines for monitoring blood glucose are inadequate. Current guidelines recommend monitoring blood glucose at the following times: baseline, at the initiation of each cycle for 12 weeks, and then every 3-6 weeks thereafter. We propose the following schedule for monitoring blood glucose in patients receiving ICI therapy: baseline, twice weekly for the first six cycles, and then once weekly thereafter. This proposed update is supported by our patient's rapid onset of hyperglycemia and other case reports and reviews showing that most patients with this diagnosis have an initial presentation of DKA. Detecting hyperglycemia and starting treatment early is important in the prevention of acute complications from uncontrolled T1DM, like DKA.
This case adds to the existing body of literature and provides support for more frequent monitoring of blood glucose in patients receiving ICI therapy. Blood glucose monitoring is a simple, reliable, low risk, and inexpensive laboratory test that should be used in patients receiving ICI therapy to ensure prompt diagnosis and treatment of T1DM.
免疫检查点抑制剂(ICIs)通过抑制 T 细胞激活来治疗多种类型的恶性肿瘤,从而促进癌细胞的破坏。这种抑制也会导致自身免疫性疾病,如内分泌疾病。
我们报告了一例 78 岁男性恶性间皮瘤患者,接受 ICI 联合治疗后出现糖尿病酮症酸中毒(DKA),无糖尿病或高血糖病史。患者被收入重症监护病房,接受静脉(IV)补液和 IV 胰岛素治疗 DKA。患者被诊断为新诊断的 ICI 治疗引起的 1 型糖尿病(T1DM)。
约 75%的诊断为 ICI 诱导的 T1DM 的患者最初表现为 DKA。加上该患者血糖迅速升高,提示目前的血糖监测指南不够充分。目前的指南建议在以下时间监测血糖:基线、每个周期开始时的 12 周内,然后每 3-6 周监测一次。我们建议接受 ICI 治疗的患者监测血糖的方案如下:基线,前 6 个周期每周监测两次,然后每周监测一次。我们的患者血糖迅速升高,以及其他病例报告和综述表明,大多数诊断为 T1DM 的患者最初表现为 DKA,支持这一更新方案。早期发现高血糖并开始治疗对于预防未经控制的 T1DM 引起的急性并发症(如 DKA)非常重要。
本病例增加了现有文献,并为接受 ICI 治疗的患者更频繁地监测血糖提供了支持。血糖监测是一种简单、可靠、低风险、廉价的实验室检查,应在接受 ICI 治疗的患者中使用,以确保及时诊断和治疗 T1DM。