Bellmunt Joaquim, Powles Thomas, Park Se Hoon, Voog Eric, Valderrama Begona P, Gurney Howard, Ullén Anders, Loriot Yohann, Sridhar Srikala S, Tsuchiya Norihiko, Sternberg Cora N, Aragon-Ching Jeanny B, Petrylak Daniel P, Climent Duran Miguel A, Tyroller Karin, Hoffman Jason, Jacob Natalia, Grivas Petros, Gupta Shilpa
Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Centre for Experimental Cancer Medicine, Barts Cancer Institute, Queen Mary University of London, St Bartholomew's Hospital, London, UK.
Eur Urol. 2025 Jun 3. doi: 10.1016/j.eururo.2025.05.017.
In the JAVELIN Bladder 100 randomized phase 3 trial (N = 700), avelumab first-line maintenance plus best supportive care (BSC) significantly prolonged overall survival (OS; primary endpoint) and progression-free survival (PFS) versus BSC alone in patients with advanced urothelial carcinoma (aUC) without progression after first-line platinum-based chemotherapy (PBC). Here, we report exploratory analyses of subgroups with nonvisceral metastases at the start of PBC (including bone metastases) or lymph node-only disease at randomization. The median OS with avelumab versus control in patients with nonvisceral metastases (n = 318) was 31.4 versus 17.1 mo (hazard ratio [HR], 0.60 [95% confidence interval {CI}, 0.45-0.79]), and in patients with lymph node-only disease (n = 102), it was 31.9 versus 22.7 mo (HR, 0.86 [95% CI, 0.51-1.47]). In patients with nonvisceral metastases, prolonged OS was observed with avelumab irrespective of the response to PBC or PBC regimen received. PFS analyses favored avelumab over control in all the subgroups. Incidences of avelumab-related adverse events were similar across the subgroups. Limitations include small sample sizes and the exploratory nature of analyses. Overall, exploratory analyses suggest that in first-line PBC-treated patients without progression, avelumab maintenance is effective and has a manageable toxicity profile in patients with aUC who have nonvisceral metastases or lymph node-only disease.
在JAVELIN Bladder 100随机3期试验(N = 700)中,与单纯最佳支持治疗(BSC)相比,阿维鲁单抗一线维持治疗加BSC显著延长了一线铂类化疗(PBC)后未进展的晚期尿路上皮癌(aUC)患者的总生存期(OS;主要终点)和无进展生存期(PFS)。在此,我们报告了对PBC开始时无内脏转移(包括骨转移)或随机分组时仅为淋巴结疾病的亚组进行的探索性分析。阿维鲁单抗组与对照组相比,无内脏转移患者(n = 318)的中位OS为31.4个月对17.1个月(风险比[HR],0.60[95%置信区间{CI},0.45 - 0.79]),仅淋巴结疾病患者(n = 102)的中位OS为31.9个月对22.7个月(HR,0.86[95%CI,0.51 - 1.47])。在无内脏转移的患者中,无论对PBC的反应或接受的PBC方案如何,阿维鲁单抗均观察到OS延长。PFS分析显示在所有亚组中阿维鲁单抗优于对照组。各亚组中阿维鲁单抗相关不良事件的发生率相似。局限性包括样本量小和分析的探索性。总体而言,探索性分析表明,在一线PBC治疗后未进展的患者中,阿维鲁单抗维持治疗对有非内脏转移或仅淋巴结疾病的aUC患者有效且毒性可控。