University of Washington, Fred Hutchinson Cancer Center, Seattle, WA.
University Hospitals Seidman Cancer Center, Cleveland, OH.
Clin Genitourin Cancer. 2024 Dec;22(6):102238. doi: 10.1016/j.clgc.2024.102238. Epub 2024 Oct 17.
In JAVELIN Bladder 100, avelumab first-line maintenance (1LM) improved overall survival (OS) and progression-free survival (PFS) in patients with locally advanced/metastatic urothelial carcinoma (la/mUC) without progression following 1L platinum-based chemotherapy (PBC) versus best supportive care. PATRIOT-II describes real-world outcomes with avelumab 1LM.
This observational, retrospective study of avelumab 1LM in US community/academic centers used medical record data collected from avelumab initiation for ≥12 months to assess survival, safety, and healthcare resource utilization; analyses are descriptive.
The study included 160 patients from 37 centers (median age, 70 years; 77% male). Avelumab 1LM was initiated at a median of 4 weeks (IQR 3-6) after PBC completion. Median follow-up from avelumab 1LM was 16 months (IQR 11-21). At study end, 19.4% of patients continued avelumab; 73.7% had discontinued due to progression, adverse events (AEs), or performance status deterioration. Median PFS and OS from avelumab initiation were 5.4 months (95% CI, 3.8-6.9) and 24.4 months (95% CI, 20.4-28.4), respectively. Grade ≥3 treatment-related AEs (TRAEs) occurred in 15 patients (9.4%); 35 (21.9%) had any-grade immune-related AEs, and 23 (14.3%) received high-dose systemic corticosteroids for AEs. Forty-four patients (27.5%) were hospitalized during the avelumab treatment period, of whom 13 (8.1%) were hospitalized due to TRAEs. Limitations of this study include a small sample size, potential selection bias, and missing/unknown data.
These results align with the JAVELIN Bladder 100 clinical trial and other real-world studies, supporting avelumab 1LM use in patients with la/mUC without progression following 1L PBC.
在 JAVELIN Bladder 100 研究中,avelumab 一线维持治疗(1LM)改善了局部晚期/转移性尿路上皮癌(la/mUC)患者的总生存期(OS)和无进展生存期(PFS),这些患者在接受 1L 铂类化疗(PBC)后没有进展,并且对比了最佳支持护理。PATRIOT-II 描述了avelumab 1LM 的真实世界结果。
这项在美国社区/学术中心进行的观察性、回顾性研究使用了avelumab 1LM 起始治疗后至少 12 个月的病历数据,以评估生存率、安全性和医疗资源利用情况;分析是描述性的。
该研究纳入了 37 个中心的 160 名患者(中位年龄 70 岁,77%为男性)。avelumab 1LM 于 PBC 完成后中位 4 周(IQR 3-6)开始。avelumab 1LM 中位随访时间为 16 个月(IQR 11-21)。研究结束时,19.4%的患者继续使用avelumab;73.7%的患者因疾病进展、不良事件(AE)或体能状态恶化而停止治疗。从 avelumab 起始的中位 PFS 和 OS 分别为 5.4 个月(95%CI,3.8-6.9)和 24.4 个月(95%CI,20.4-28.4)。15 名患者(9.4%)发生了≥3 级治疗相关不良事件(TRAE);35 名患者(21.9%)发生了任何级别免疫相关不良事件,23 名患者(14.3%)因 AE 接受了高剂量全身皮质类固醇治疗。44 名患者(27.5%)在 avelumab 治疗期间住院,其中 13 名(8.1%)因 TRAE 住院。本研究的局限性包括样本量小、潜在选择偏倚和缺失/未知数据。
这些结果与 JAVELIN Bladder 100 临床试验和其他真实世界研究一致,支持在 1L PBC 后无进展的 la/mUC 患者中使用 avelumab 1LM。