Departments of Medical Oncology & Urology, The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins Medical Institutions, Baltimore, MD, USA.
University of Washington, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Future Oncol. 2024 Feb;20(4):179-190. doi: 10.2217/fon-2023-0492. Epub 2023 Sep 6.
Results from JAVELIN Bladder 100 established avelumab (anti-PD-L1) first-line maintenance as the standard-of-care treatment for patients with advanced urothelial carcinoma (UC) that has not progressed with first-line platinum-based chemotherapy. We describe the design of JAVELIN Bladder Medley (NCT05327530), an ongoing phase II, multicenter, randomized, open-label, parallel-arm, umbrella trial. Overall, 252 patients with advanced UC who are progression-free following first-line platinum-based chemotherapy will be randomized 1:2:2:2 to receive maintenance therapy with avelumab alone (control group) or combined with sacituzumab govitecan (anti-Trop-2/topoisomerase inhibitor conjugate), M6223 (anti-TIGIT) or NKTR-255 (recombinant human IL-15). Primary end points are progression-free survival per investigator and safety/tolerability of the combination regimens. Secondary end points include overall survival, objective response and duration of response per investigator, and pharmacokinetics.
JAVELIN Bladder 100 研究结果确立了avelumab(抗 PD-L1)作为一线维持治疗,用于一线铂类化疗后未进展的晚期尿路上皮癌(UC)患者的标准治疗。我们描述了 JAVELIN Bladder Medley(NCT05327530)的设计,这是一项正在进行的 II 期、多中心、随机、开放标签、平行臂、伞式试验。总体而言,252 例一线铂类化疗后无进展的晚期 UC 患者将按照 1:2:2:2 的比例随机分为接受avelumab 单药(对照组)或联合 sacituzumab govitecan(抗 Trop-2/拓扑异构酶抑制剂偶联物)、M6223(抗 TIGIT)或 NKTR-255(重组人 IL-15)维持治疗。主要终点是研究者评估的无进展生存期和联合方案的安全性/耐受性。次要终点包括研究者评估的总生存期、客观缓解率和缓解持续时间,以及药代动力学。