Furubayashi Nobuki, Tsujita Jiro, Takayama Azusa, Nakashima Shin, Nakamura Motonobu, Negishi Takahito
Department of Urology, NHO Kyushu Cancer Center, Fukuoka 811-1395, Japan.
Cancers (Basel). 2025 Jul 23;17(15):2447. doi: 10.3390/cancers17152447.
Commonly characterized by limited metastatic sites, low tumor burden has been associated with favorable patient outcomes in various malignancies. However, its prognostic relevance in avelumab maintenance therapy for advanced urothelial carcinoma (UC) remains incompletely defined. We retrospectively analyzed 26 patients with advanced UC who received avelumab maintenance therapy following disease control with first-line platinum-based chemotherapy between March 2021 and May 2025. Patients were categorized by their metastatic pattern at a chemotherapy initiation: lymph node-only (as a surrogate for low tumor burden), non-visceral (excluding visceral organ involvement, but including bone), or visceral disease. Survival outcomes were assessed using the Kaplan-Meier method. Among the cohort, 46.2% had lymph node-only metastasis and 57.7% had non-visceral disease. The median progression-free survival (PFS) and overall survival (OS) from the start of avelumab were 5.6 months and 21.7 months, respectively. OS from the initiation of platinum-based chemotherapy was 28.7 months. Patients with lymph node-only metastasis demonstrated significantly longer OS from chemotherapy initiation compared with those with other metastatic patterns (41.1 vs. 22.9 months, = 0.044). However, the PFS and OS from avelumab initiation did not significantly differ. No survival benefit was observed for patients with non-visceral disease compared with those with visceral metastases. Lymph node-only metastasis, representing low tumor burden, was associated with significantly improved long-term survival in advanced UC patients undergoing avelumab maintenance following chemotherapy. These findings support the clinical utility of baseline tumor burden and metastatic pattern in risk stratification and shared decision-making for maintenance therapy in advanced UC.
低肿瘤负荷通常表现为转移部位有限,在各种恶性肿瘤中,它与患者的良好预后相关。然而,其在阿维鲁单抗维持治疗晚期尿路上皮癌(UC)中的预后相关性仍未完全明确。我们回顾性分析了26例晚期UC患者,这些患者在2021年3月至2025年5月期间接受了一线铂类化疗疾病控制后接受阿维鲁单抗维持治疗。患者根据化疗开始时的转移模式进行分类:仅淋巴结转移(作为低肿瘤负荷的替代指标)、非内脏转移(不包括内脏器官受累,但包括骨转移)或内脏转移。使用Kaplan-Meier方法评估生存结果。在该队列中,46.2%的患者仅发生淋巴结转移,57.7%的患者为非内脏转移。从开始使用阿维鲁单抗起,中位无进展生存期(PFS)和总生存期(OS)分别为5.6个月和21.7个月。从开始铂类化疗起的OS为28.7个月。与其他转移模式的患者相比,仅发生淋巴结转移的患者从化疗开始起的OS显著更长(41.1个月对22.9个月,P = 0.044)。然而,从开始使用阿维鲁单抗起的PFS和OS没有显著差异。与内脏转移患者相比,非内脏转移患者未观察到生存获益。仅淋巴结转移代表低肿瘤负荷,与接受化疗后阿维鲁单抗维持治疗的晚期UC患者的长期生存显著改善相关。这些发现支持了基线肿瘤负荷和转移模式在晚期UC维持治疗的风险分层和共同决策中的临床应用。