Kaiser Permanente Southern California, Riverside, CA 92505, USA.
Merck Healthcare KGaA, 64293 Darmstadt, Germany.
Curr Oncol. 2024 Sep 21;31(9):5662-5676. doi: 10.3390/curroncol31090420.
For patients with locally advanced/metastatic urothelial carcinoma (la/mUC), first-line (1L) treatment with platinum-based chemotherapy (PBC) followed by avelumab 1L maintenance (1LM) is a recommended therapy per treatment guidelines in patients without disease progression. However, contemporary real-world (rw) data among patients receiving this treatment are necessary to understand clinical outcomes and optimal treatment sequencing. This retrospective cohort study analyzed rw treatment patterns and clinical outcomes, including overall survival (rwOS) and progression-free survival (rwPFS), in patients with la/mUC receiving avelumab 1LM. From the Flatiron Health database, 214 patients who received avelumab 1LM following 1L PBC were included. From the start of avelumab 1LM, median rwOS was 23.8 months (95% CI: 18.2-not estimable [NE]) and median rwPFS was 5.1 months (95% CI: 4.1-7.0). A total of 96 patients received second-line (2L) therapy, with 53 receiving enfortumab vedotin (EV). From the start of 2L EV, median rwOS was 11.2 months (95% CI: 6.8-NE) and median rwPFS was 4.9 months (95% CI: 3.9-8.8). Treatment patterns and clinical outcomes in this study align with guidelines and outcomes observed in the JAVELIN Bladder 100 and EV-301 clinical trials and other rw studies, supporting the use of 1L PBC followed by avelumab 1LM and 2L EV for eligible patients.
对于局部晚期/转移性尿路上皮癌(la/mUC)患者,如果在没有疾病进展的情况下,根据治疗指南,一线(1L)治疗采用铂类化疗(PBC),随后采用avelumab 1L 维持(1LM),这是一种推荐的治疗方法。然而,需要了解接受这种治疗的患者的当代真实世界(rw)数据,以了解临床结果和最佳治疗顺序。这项回顾性队列研究分析了接受 avelumab 1LM 治疗的 la/mUC 患者的 rw 治疗模式和临床结果,包括总生存期(rwOS)和无进展生存期(rwPFS)。从 Flatiron Health 数据库中,纳入了 214 名在接受 1L PBC 后接受 avelumab 1LM 治疗的患者。从 avelumab 1LM 开始,中位 rwOS 为 23.8 个月(95%CI:18.2-NE),中位 rwPFS 为 5.1 个月(95%CI:4.1-7.0)。共有 96 名患者接受二线(2L)治疗,其中 53 名接受 enfortumab vedotin(EV)治疗。从开始使用 2L EV 起,中位 rwOS 为 11.2 个月(95%CI:6.8-NE),中位 rwPFS 为 4.9 个月(95%CI:3.9-8.8)。这项研究中的治疗模式和临床结果与指南一致,并且与 JAVELIN Bladder 100 和 EV-301 临床试验以及其他 rw 研究中的观察结果一致,支持对符合条件的患者采用 1L PBC 后继以 avelumab 1LM 和 2L EV 治疗。