Hovelroud Rachel, Goh Xiu Ming Sarah, McLeod Donald S A, Donovan Peter J, Ng Gary, Mungomery Maree
Department of Diabetes and Endocrinology, Townsville University Hospital, Douglas QLD 4814, Australia.
Department of Diabetes and Endocrinology, Royal Brisbane & Women's Hospital, Herston QLD 4006, Australia.
JCEM Case Rep. 2024 Nov 25;2(12):luae212. doi: 10.1210/jcemcr/luae212. eCollection 2024 Dec.
Enfortumab vedotin is a novel antibody-drug conjugate (ADC) approved to treat urothelial carcinoma. One rarely reported adverse effect has been life-threatening diabetic ketoacidosis (DKA) driven by profound insulin resistance. We report a case of a 62-year-old nondiabetic woman with metastatic urothelial carcinoma who experienced DKA following her third dose of enfortumab vedotin, with extreme insulin requirements of > 1000 units daily, and full resolution of insulin requirement by day 7 of admission. Including this case, 3 of 9 reported patients with enfortumab vedotin-associated DKA have survived. Monomethyl auristatin E (MMAE), the cytotoxic component of enfortumab vedotin, is the likely cause, although the exact mechanism remains unclear. This rare clinical event challenges the usual protocols and practice surrounding insulin infusion administration, and this case provides evidence to assist in understanding the mechanism by which enfortumab vedotin causes ketoacidosis.
安维汀(Enfortumab vedotin)是一种被批准用于治疗尿路上皮癌的新型抗体药物偶联物(ADC)。一种罕见的不良反应是由严重胰岛素抵抗导致的危及生命的糖尿病酮症酸中毒(DKA)。我们报告了一例62岁非糖尿病转移性尿路上皮癌女性患者,在接受第三剂安维汀治疗后发生DKA,每日胰岛素需求量极高,超过1000单位,入院第7天时胰岛素需求完全恢复正常。包括该病例在内,9例报告的与安维汀相关的DKA患者中有3例存活。安维汀的细胞毒性成分单甲基奥瑞他汀E(MMAE)可能是病因,尽管确切机制尚不清楚。这一罕见的临床事件对胰岛素输注给药的常规方案和实践提出了挑战,该病例为协助理解安维汀导致酮症酸中毒的机制提供了证据。