化疗耐药的转移性尿路上皮癌患者通过连续血液透析滤过和胰岛素注射等多学科治疗成功治愈恩福单抗维多汀诱发的发热性中性粒细胞减少症和高血糖症:病例报告。

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2024-08-12 eCollection Date: 2024-01-01 DOI:10.1159/000540354
Ayatsugu Otsuka, Norifumi Sawada, Ryosuke Suda, Fumiakira Yano, Takuya Osada, Yuko Otake, Hiroshi Shimura, Takanori Mochizuki, Daiki Harada, Junko Goto, Tomomi Watanabe, Tadatsugu Hosokawa, Satoru Kira, Kyoichiro Tsuchiya, Takeshi Moriguchi, Takahiko Mitsui
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引用次数: 0

摘要

简介Enfortumab vedotin(EV)是一种抗体-药物共轭物,结合了一种靶向内皮素-4的单克隆抗体和一种高效微管破坏剂。EV有望成为曾接受过铂类化疗和PD-1/PD-L1抑制剂治疗的尿路上皮癌的三线治疗候选药物。很少有患者出现不明原因的高血糖:我们描述了一名 72 岁的亚洲男子,他患有轻度肥胖、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。他在服用 3 次 EV 后出现高血糖和发热性中性粒细胞减少症。他的高血糖为 489 mg/dL,开始持续静脉注射胰岛素(CVII)。患者的静脉胰岛素需求量达到峰值,每天 316 单位。他还出现了发热性中性粒细胞减少症,并因此引发了败血症,导致急性肾损伤。为了治疗脓毒症,患者开始接受连续血液透析滤过(CHDF)和抗生素治疗。CHDF 治疗后,血糖水平逐渐下降,CHDF 持续了 14 天。从 CHDF 中释放的时间与 EV 的消除半衰期(3.4 天)相关。CVII 治疗 26 天后,患者最终从重症监护室出院:本病例表明,在转移性尿路上皮癌治疗过程中,EV 引起的无法控制的高血糖可以通过 CVII 和 CHDF 得到有效控制,直到 EV 的不良反应消失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enfortumab Vedotin-Induced Febrile Neutropenia and Hyperglycemia Successfully Treated with Multidisciplinary Treatment Including Continuous Hemodialysis Filtration and Insulin Injection in a Patient with Chemo-Resistant Metastatic Urothelial Carcinoma: A Case Report.

Introduction: 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.

Case presentation: 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.

Conclusion: 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.

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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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