Arecco Anna, Petolicchio Cristian, Pastorino Alessandro, Tanda Enrica Teresa, Vera Lara, Boschetti Mara, Cocchiara Francesco, Maggi Davide Carlo, Ferone Diego, Gatto Federico
Endocrinology Unit, Department of Internal Medicine and Medical Specialties, School of Medical and Pharmaceutical Sciences, University of Genova, Genova, Italy.
Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Front Endocrinol (Lausanne). 2025 Mar 25;16:1550702. doi: 10.3389/fendo.2025.1550702. eCollection 2025.
Immune checkpoint inhibitors (ICIs) have revolutionised the cancer treatment landscape in the last decades, improving the outcome of several tumours, such as cutaneous squamous cell carcinoma (cSCC). ICIs are antibodies blocking several immune checkpoint pathways, as cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) and programmed cell death 1 (PD-1) with its ligand PD-L1. However, the activation of immune response can cause a broad range of side effects, called immune-related adverse events (irAEs). Endocrine irAEs are mainly represented by thyroid dysfunctions (thyrotoxicosis or hypothyroidism) and hypophysitis, while adrenal insufficiency and diabetes mellitus (DM) are less common. Diabetic ketoacidosis (DKA) is a potential life-threatening presentation of ICI-induced insulin-dependent DM (IDDM). This report presents a rare case of DKA and IDDM secondary to anti-PD-1 antibody cemiplimab therapy, and this is the third described in the literature to date.
We describe the case of a 62-year-old female patient with metastatic perianal squamous cell carcinoma who developed DKA and IDDM after the fifth cycle of cemiplimab. Hyperglycemia (1187 mg/dL), metabolic acidosis (pH 7.27) with bicarbonate levels of 11.9 mmol/L, arterial partial pressure of carbon dioxide of 25.7 mmHg with increased anion gap (equal to 25), and hyperketonuria were present. Adequate glycaemic control was difficult to maintain, and intravenously therapy (insulin, sodium bicarbonate, potassium, and fluids) was required for a long time. Subcutaneous basal-bolus insulin treatment was started, but glycaemic control was scarce, also due to the concomitant administration of prednisone for immune-related hepatotoxicity, until the subject's death.
This report underlines the importance of the awareness on endocrine irAEs with ICIs, particularly life-threatening DKA. A baseline assessment of glycemia and glycated hemoglobin is mandatory, and we recommend a close monitoring of glycemic trend over time during ICIs therapy. Patients and their caregivers should be informed and counselled to recognise DKA signs and symptoms.
在过去几十年中,免疫检查点抑制剂(ICIs)彻底改变了癌症治疗格局,改善了多种肿瘤的治疗结果,如皮肤鳞状细胞癌(cSCC)。ICIs是阻断多种免疫检查点途径的抗体,如细胞毒性T淋巴细胞相关抗原4(CTLA-4)以及程序性细胞死亡蛋白1(PD-1)及其配体PD-L1。然而,免疫反应的激活可导致广泛的副作用,称为免疫相关不良事件(irAEs)。内分泌irAEs主要表现为甲状腺功能障碍(甲状腺毒症或甲状腺功能减退)和垂体炎,而肾上腺功能不全和糖尿病(DM)则较少见。糖尿病酮症酸中毒(DKA)是ICI诱导的胰岛素依赖型糖尿病(IDDM)的一种潜在危及生命的表现形式。本报告介绍了1例罕见的继发于抗PD-1抗体西米普利单抗治疗的DKA和IDDM病例,这是迄今为止文献中描述的第3例。
我们描述了1例62岁转移性肛周鳞状细胞癌女性患者,在接受西米普利单抗第5个周期治疗后发生了DKA和IDDM。存在高血糖(1187mg/dL)、代谢性酸中毒(pH 7.27),碳酸氢盐水平为11.9mmol/L,动脉血二氧化碳分压为25.7mmHg,阴离子间隙增加(等于25),以及高酮尿症。难以维持充分的血糖控制,需要长时间进行静脉治疗(胰岛素、碳酸氢钠、钾和液体)。开始皮下基础-餐时胰岛素治疗,但由于同时使用泼尼松治疗免疫相关肝毒性,血糖控制不佳,直至患者死亡。
本报告强调了对ICIs相关内分泌irAEs,尤其是危及生命的DKA提高认识的重要性。必须进行血糖和糖化血红蛋白的基线评估,并且我们建议在ICIs治疗期间密切监测血糖随时间的变化趋势。应告知患者及其护理人员并给予指导,使其认识DKA的体征和症状。