Dana-Farber Cancer Institute.
University of North Carolina Healthcare.
Clin J Oncol Nurs. 2021 Apr 1;25(2):E1-E9. doi: 10.1188/21.CJON.E1-E9.
Many patients with locally advanced or metastatic urothelial carcinoma (mUC) need additional treatment options beyond PD-1 or PD-L1 inhibitors and platinum-based chemotherapies. Enfortumab vedotin-ejfv (EV) is an antibody-drug conjugate directed at Nectin-4 that received accelerated approval for treatment of adults with locally advanced or mUC previously treated with PD-1/PD-L1 inhibitors and platinum- containing chemotherapy in the neoadjuvant/adjuvant, locally advanced, or metastatic settings.
This article provides practical considerations and recommendations regarding common and potentially treatment-limiting adverse events that may arise with EV therapy.
The clinical data that supported the approval of EV are reviewed, and supporting safety and management considerations are provided based on the authors' experience.
EV therapy can be optimized through patient and caregiver education, proactive patient monitoring, early identification of adverse events, and timely intervention to alleviate symptoms.
许多局部晚期或转移性尿路上皮癌(mUC)患者需要除 PD-1 或 PD-L1 抑制剂和铂类化疗之外的其他治疗选择。Enfortumab vedotin-ejfv(EV)是一种针对 Nectin-4 的抗体药物偶联物,在新辅助/辅助、局部晚期或转移性环境中,既往接受过 PD-1/PD-L1 抑制剂和含铂化疗治疗的局部晚期或转移性 mUC 成人患者中,获得了加速批准。
本文提供了与 EV 治疗相关的常见且可能具有治疗限制的不良反应的实用注意事项和建议。
回顾了支持 EV 批准的临床数据,并根据作者的经验提供了支持安全性和管理注意事项。
通过患者和护理人员教育、主动患者监测、早期识别不良反应以及及时干预以缓解症状,可以优化 EV 治疗。