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SGNDV-001:在人表皮生长因子受体2(HER2)表达的局部晚期或转移性尿路上皮癌中,迪西他单抗维泊妥珠单抗联合帕博利珠单抗的研究

SGNDV-001: disitamab vedotin with pembrolizumab in HER2-expressing locally advanced or metastatic urothelial carcinoma.

作者信息

Powles Thomas B, Grande Enrique, Alimohamed Nimira, Oliveira Niara, Sridhar Srikala S, Drakaki Alexandra, Kanesvaran Ravindran, Loriot Yohann, Necchi Andrea, Franco Sonia, Jiang Dingfeng, Apolinario Kristel, Zhang Wei, Galsky Matthew D

机构信息

Barts Cancer Centre, Queen Mary University of London, London, UK.

Department of Medical Oncology, MD Anderson Cancer Center Madrid, Madrid, Spain.

出版信息

Future Oncol. 2025 Jul 29:1-8. doi: 10.1080/14796694.2025.2535280.

Abstract

INTRODUCTION

Platinum-based chemotherapy for the treatment of locally advanced or metastatic urothelial carcinoma (la/mUC), has been the first-line standard of care for many decades. Enfortumab vedotin, an antibody-drug conjugate, combined with pembrolizumab, a programmed death 1 (PD-1) inhibitor, recently demonstrated improved efficacy versus chemotherapy in la/mUC. Since 60%-80% of patients with UC have tumors expressing human epidermal growth factor receptor 2 (HER2), HER2-directed vedotin-based antibody-drug conjugates may also be beneficial in la/mUC.

PATIENTS AND METHODS

The phase 3 trial SGNDV-001 (C5731001; NCT05911295) is evaluating disitamab vedotin (HER2-directed antibody-drug conjugate) with pembrolizumab compared with chemotherapy in treatment-naive patients with HER2-expressing la/mUC. Dual primary endpoints are progression-free survival (per blinded independent central review) and overall survival. Potential synergistic effects of disitamab vedotin and pembrolizumab could establish this combination as a novel therapeutic option for HER2-expressing la/mUC.

摘要

引言

几十年来,铂类化疗一直是治疗局部晚期或转移性尿路上皮癌(la/mUC)的一线标准治疗方案。恩杂鲁胺,一种抗体药物偶联物,与程序性死亡1(PD-1)抑制剂派姆单抗联合使用,最近在la/mUC治疗中显示出比化疗更好的疗效。由于60%-80%的UC患者肿瘤表达人表皮生长因子受体2(HER2),基于HER2导向的恩杂鲁胺抗体药物偶联物在la/mUC中可能也有益处。

患者与方法

3期试验SGNDV-001(C5731001;NCT05911295)正在评估迪西他单抗(HER2导向的抗体药物偶联物)联合派姆单抗与化疗相比,在初治的HER2表达的la/mUC患者中的疗效。双重主要终点是无进展生存期(由盲态独立中央审查)和总生存期。迪西他单抗和派姆单抗的潜在协同作用可能使这种联合治疗成为HER2表达的la/mUC的一种新型治疗选择。

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