美国接受阿维单抗一线维持治疗的局部晚期或转移性尿路上皮癌患者的实际治疗模式、排序和疗效。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-09-21 DOI:10.3390/curroncol31090420
Helen H Moon, Mairead Kearney, Seyed Hamidreza Mahmoudpour, Chiemeka Ike, Valerie Morris, Andrew Rava, Sonia Kim, Haiyan Sun, Marley Boyd, Gabriel Gomez Rey
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引用次数: 0

摘要

对于局部晚期/转移性尿路上皮癌(la/mUC)患者,根据治疗指南,在无疾病进展的患者中推荐使用铂类化疗(PBC)一线治疗(1L),然后使用阿维列单抗1L维持治疗(1LM)。然而,为了了解临床疗效和最佳治疗顺序,有必要掌握接受这种治疗的患者的当代真实世界(rw)数据。这项回顾性队列研究分析了接受阿维列单抗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)。Flatiron Health数据库共纳入了214名接受阿维列单抗1LM治疗的1L PBC患者。从开始使用阿维列单抗1LM起,中位rwOS为23.8个月(95% CI:18.2-无法估计[NE]),中位rwPFS为5.1个月(95% CI:4.1-7.0)。共有96名患者接受了二线(2L)治疗,其中53人接受了恩福单抗维多汀(EV)治疗。从 2L EV 开始,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)。本研究中的治疗模式和临床结果与 JAVELIN Bladder 100 和 EV-301 临床试验及其他 rw 研究中观察到的指南和结果一致,支持对符合条件的患者使用 1L PBC,然后使用阿维列单抗 1LM 和 2L EV。
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Real-World Treatment Patterns, Sequencing, and Outcomes in Patients with Locally Advanced or Metastatic Urothelial Carcinoma Receiving Avelumab First-Line Maintenance in the United States.

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.

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ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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