Gonçalves Lisa, Guedes Helena, Fortuna Ana Raquel, Lemos Tânia, Gramaça João, Mourão Natacha, Cunha Gonçalo, Pichel Rita, Simões Pedro, Luís Joana Alves, Freitas Rita, Dunões Inês, Spencer Ana Sofia, Marinho Joana, Costa Luís
Department of Oncology, Unidade Local de Saúde Santa Maria Lisboa, Avenida Professor Egas Moniz, 1649-035 Lisboa, Portugal.
Unidade Local de Saúde Gaia e Espinho, 4434-502 Vila Nova de Gaia, Portugal.
Cancers (Basel). 2025 Mar 6;17(5):898. doi: 10.3390/cancers17050898.
Platinum-based chemotherapy (PBC) followed by avelumab maintenance is a treatment option for patients with advanced urothelial carcinoma (aUC) patients. However, the optimal treatment sequencing in the era of antibody-drug conjugates (ADCs) is yet to be determined. Recent studies suggest that the timing of immune checkpoint inhibitor (ICI) administration may impact patient outcomes, with a potential benefit from morning infusions.
This retrospective study included 105 patients with aUC treated with avelumab in Portugal and intended to assess the safety and clinical outcomes (progression-free survival (PFS), overall survival (OS), and overall response rate (ORR)) and evaluate the impact of treatment timing (morning vs. afternoon) on patient outcomes.
The median follow-up from the start of avelumab was 17.7 months, the median PFS (mPFS) was 9.8 months (95% CI 4.9-14.7), and the median OS (mOS) was 39.5 months (95% CI 13.2-65.7). Immune-related adverse events (irAEs) were reported in 65.8% of patients, with 6.7% experiencing G3 irAEs. Among those who received a subsequent-line ADC upon disease progression (43%), the mOS from the start of avelumab was 23.1 months (95% CI 9.2-37.0). Multivariate analysis showed significant improvement in mOS with morning avelumab infusions (HR 0.35, 95% CI: 0.12-0.97, = 0.042) and a trend towards improved mPFS (HR 0.43, 95% CI: 0.179-1.02, = 0.055).
This study confirms the clinical efficacy and safety of avelumab, showing improved outcomes over JAVELIN Bladder 100 and suggesting that morning infusions may offer a survival benefit in this context. Further research is needed to optimize treatment sequencing and explore the impact of infusion timing in ICI strategies.
铂类化疗(PBC)后使用阿维鲁单抗维持治疗是晚期尿路上皮癌(aUC)患者的一种治疗选择。然而,在抗体药物偶联物(ADC)时代的最佳治疗顺序尚未确定。最近的研究表明,免疫检查点抑制剂(ICI)给药时间可能会影响患者的预后,早晨输注可能具有潜在益处。
这项回顾性研究纳入了105例在葡萄牙接受阿维鲁单抗治疗的aUC患者,旨在评估安全性和临床结局(无进展生存期(PFS)、总生存期(OS)和总缓解率(ORR)),并评估治疗时间(早晨与下午)对患者结局的影响。
从开始使用阿维鲁单抗起的中位随访时间为17.7个月,中位PFS(mPFS)为9.8个月(95%CI 4.9 - 14.7),中位OS(mOS)为39.5个月(95%CI 13.2 - 65.7)。65.8%的患者报告了免疫相关不良事件(irAE),6.7%的患者发生3级irAE。在疾病进展后接受后续线ADC治疗的患者中(43%),从开始使用阿维鲁单抗起的mOS为23.1个月(95%CI 9.2 - 37.0)。多因素分析显示,早晨输注阿维鲁单抗使mOS有显著改善(HR 0.35,95%CI:0.12 - 0.97,P = 0.042),且mPFS有改善趋势(HR 0.43,95%CI:0.179 - 1.02,P = 0.055)。
本研究证实了阿维鲁单抗的临床疗效和安全性,显示出比JAVELIN Bladder 100更好的结局,并表明在这种情况下早晨输注可能带来生存益处。需要进一步研究以优化治疗顺序,并探索输注时间在ICI策略中的影响。