Otsuka Ayatsugu, Sawada Norifumi, Suda Ryosuke, Yano Fumiakira, Osada Takuya, Otake Yuko, Shimura Hiroshi, Mochizuki Takanori, Harada Daiki, Goto Junko, Watanabe Tomomi, Hosokawa Tadatsugu, Kira Satoru, Tsuchiya Kyoichiro, Moriguchi Takeshi, Mitsui Takahiko
Department of Urology, Interdisciplinary Graduate School of Medicine, University of Yamanashi, Chuo City, Yamanashi, Japan.
Department of Emergency Intensive Care Medicine, Interdisciplinary Graduate School of Medicine, University of Yamanashi, Chuo City, Yamanashi, Japan.
Case Rep Oncol. 2024 Aug 12;17(1):891-899. doi: 10.1159/000540354. eCollection 2024 Jan-Dec.
Enfortumab vedotin (EV) is an antibody-drug conjugate combining a monoclonal antibody targeting nectin-4 with a highly potent microtubule disrupting agent. EV is expected to be a candidate for the third-line treatment for urothelial carcinoma previously treated with platinum-based chemotherapy and PD-1/PD-L1 inhibitors. Very few cases of patients experienced hyperglycemia of unknown cause.
We describe a 72-year-old Asian man with mild obesity, type 2 diabetes, hyperlipidemia, hypertension, and chemo-resistant metastatic urothelial carcinoma. He developed hyperglycemia and febrile neutropenia after 3 doses of EV. He had hyperglycemia of 489 mg/dL and was started on continuous intravenous insulin infusion (CVII). The patient's intravenous insulin requirements peaked at 316 units per day. He also developed febrile neutropenia and consequent sepsis caused acute kidney injury. Continuous hemodialysis filtration (CHDF) together with antibiotics were started to treat the septic condition. The blood glucose level gradually decreased after CHDF treatment and CHDF was continued for 14 days. The timing of liberation from CHDF correlated with the elimination half-life of EV of 3.4 days. CVII was treated for 26 days and the patient was finally released from the intensive care unit.
This case indicates that the uncontrollable hyperglycemia induced by EV during metastatic urothelial carcinoma treatment is effectively managed with CVII and CHDF until the elimination of the adverse effect of EV.
恩杂鲁胺(EV)是一种抗体药物偶联物,它将靶向nectin-4的单克隆抗体与一种高效的微管破坏剂结合在一起。EV有望成为先前接受过铂类化疗和PD-1/PD-L1抑制剂治疗的尿路上皮癌三线治疗的候选药物。很少有患者出现不明原因的高血糖症。
我们描述了一名72岁的亚洲男性,患有轻度肥胖、2型糖尿病、高脂血症、高血压和化疗耐药的转移性尿路上皮癌。他在接受3剂EV治疗后出现高血糖和发热性中性粒细胞减少。他的血糖高达489mg/dL,并开始持续静脉输注胰岛素(CVII)。患者静脉胰岛素需求量峰值达到每天316单位。他还出现了发热性中性粒细胞减少,随后的败血症导致急性肾损伤。开始采用持续血液透析滤过(CHDF)联合抗生素治疗败血症。CHDF治疗后血糖水平逐渐下降,CHDF持续了14天。从CHDF中解脱的时间与EV的消除半衰期3.4天相关。CVII治疗了26天,患者最终从重症监护病房出院。
该病例表明,在转移性尿路上皮癌治疗期间,由EV引起的难以控制的高血糖症可通过CVII和CHDF有效管理,直至EV的不良反应消除。