Gupta S, Climent Duran M A, Sridhar S S, Powles T, Bellmunt J, Park S H, Gurney H, Tsuchiya N, Petrylak D P, Tomita Y, di Pietro A, Manitz J, Tyroller K, Hoffman J, Jacob N, Grivas P
Taussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, USA.
Instituto Valenciano de Oncología, Valencia, Spain.
ESMO Open. 2025 Apr;10(4):104506. doi: 10.1016/j.esmoop.2025.104506. Epub 2025 Mar 18.
In the JAVELIN Bladder 100 phase III trial, avelumab first-line (1L) maintenance plus best supportive care (BSC) significantly prolonged overall survival (OS) versus BSC alone in patients with locally advanced or metastatic urothelial carcinoma (la/mUC) without progression following platinum-based chemotherapy. Older age (≥65 years) is a known risk factor for bladder cancer with a median age at diagnosis of 73.0 years. We report exploratory analyses in subgroups based on older age (≥65 years).
Eligible patients with la/mUC without progression after 1L platinum-based chemotherapy were randomized to receive avelumab plus BSC (n = 350) or BSC alone (n = 350). This exploratory analysis included subgroups aged ≥65 years, ≥65-<75 years, ≥75 years, and the subset aged ≥80 years. OS (primary endpoint) and progression-free survival (PFS) from randomization were analyzed using the Kaplan-Meier method.
Of 700 patients, 464 (66.3%) were aged ≥65 years. Median OS with avelumab plus BSC versus BSC alone was 26.1 versus 15.5 months (hazard ratio 0.70, 95% confidence interval 0.56-0.89) in all patients aged ≥65 years and 28.7 versus 17.1, 24.0 versus 13.5, and 24.9 versus 10.0 months, respectively, in patients aged ≥65-<75, ≥75, and ≥80 years. PFS analyses favored avelumab plus BSC versus BSC alone in all subgroups. No new safety concerns were identified in patients aged ≥65 years, including those treated for ≥12 months. Quality-adjusted time without symptoms or toxicity was 4.57 months longer with avelumab plus BSC versus BSC alone (a 30.35% relative improvement). Limitations include small sample size for the ≥80-year age subgroup and the exploratory design.
These exploratory analyses support the efficacy and tolerability of avelumab 1L maintenance in patients aged ≥65 years with la/mUC that has not progressed following chemotherapy, suggesting that older age should not solely prevent a patient from receiving avelumab 1L maintenance.
在JAVELIN Bladder 100 III期试验中,与单纯最佳支持治疗(BSC)相比,阿维鲁单抗一线(1L)维持治疗联合最佳支持治疗(BSC)显著延长了铂类化疗后未进展的局部晚期或转移性尿路上皮癌(la/mUC)患者的总生存期(OS)。老年(≥65岁)是已知的膀胱癌危险因素,诊断时的中位年龄为73.0岁。我们报告了基于老年(≥65岁)亚组的探索性分析。
符合条件的1L铂类化疗后未进展的la/mUC患者被随机分为接受阿维鲁单抗联合BSC(n = 350)或单纯BSC(n = 350)治疗。这项探索性分析包括年龄≥65岁、≥65 - <75岁、≥75岁以及≥80岁的亚组。采用Kaplan-Meier方法分析随机分组后的总生存期(主要终点)和无进展生存期(PFS)。
在700例患者中,464例(66.3%)年龄≥65岁。在所有年龄≥65岁的患者中,阿维鲁单抗联合BSC与单纯BSC相比,中位OS分别为26.1个月和15.5个月(风险比0.70,95%置信区间0.56 - 0.89);在年龄≥65 - <75岁、≥75岁和≥80岁的患者中,中位OS分别为28.7个月和17.1个月、24.0个月和13.5个月、24.9个月和10.0个月。PFS分析显示,在所有亚组中,阿维鲁单抗联合BSC均优于单纯BSC。在年龄≥65岁的患者中,包括治疗≥12个月的患者,未发现新的安全问题。与单纯BSC相比,阿维鲁单抗联合BSC的无症状或无毒性的质量调整时间长4.57个月(相对改善30.35%)。局限性包括≥80岁年龄亚组的样本量小以及探索性设计。
这些探索性分析支持了阿维鲁单抗1L维持治疗对化疗后未进展的年龄≥65岁的la/mUC患者的疗效和耐受性,表明年龄较大不应成为患者接受阿维鲁单抗1L维持治疗的唯一障碍。