Wang Yanjun, Zhong Kaihua, Tan Xingliang, Zhou Qianghua, Jiang Lijuan, Yao Kai, Wu Zhiming
Department of Urology, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Department of Urology, Meizhou People's Hospital, Meizhou, China.
Cancer Med. 2025 Feb;14(4):e70661. doi: 10.1002/cam4.70661.
Muscle-invasive urothelial carcinoma (MIUC) is a highly aggressive cancer associated with poor prognosis. Despite advancements in treatment, the optimal therapeutic approach remains unclear. Immune checkpoint inhibitors, when added to chemotherapy, have shown promise in improving patient outcomes.
This study aimed to evaluate the efficacy and safety of adjuvant tislelizumab combined with gemcitabine/cisplatin (Tisle+GC) compared to GC alone in patients with high-risk MIUC.
MATERIALS & METHODS: We conducted a retrospective analysis of 117 patients with histologically confirmed pT3/4 and pN+ MIUC treated at our center between October 2016 and March 2023. Eligible patients received either Tisle+GC or GC alone, excluding those with prior neoadjuvant therapy. We compared disease-free survival (DFS), overall survival (OS), and treatment-related adverse events (AEs) between the two groups using Cox proportional hazards models and Kaplan-Meier estimates.
The Tisle+GC group showed significantly longer median DFS (19.08 vs. 9.06 months, HR = 0.114, p < 0.001) and OS (20.07 vs. 10.63 months, HR = 0.083, p = 0.026) compared to the GC group. Nerve tract invasion was identified as a significant predictor of poor outcomes (HR = 22.1, p = 0.003). Both groups experienced manageable grade 1-2 immune-related AEs, with pruritus being the most common, followed by liver function abnormalities and thyroid disturbances. Nonhematologic toxicities in the Tisle+GC group included elevated aspartate aminotransferase and hyponatremia, while the GC group mainly reported vomiting. No treatment-related fatalities occurred.
The addition of tislelizumab to GC chemotherapy significantly improved both DFS and OS in high-risk MIUC patients. The safety profile was manageable, with immune-related AEs being predictable and not life-threatening. The findings support the potential of Tisle+GC as an effective adjuvant therapy.
Tisle+GC is a promising adjuvant treatment for high-risk MIUC, offering improved survival outcomes with a manageable safety profile. Further prospective studies are needed to confirm these results and establish the long-term benefits of this combination therapy.
肌层浸润性尿路上皮癌(MIUC)是一种侵袭性很强的癌症,预后较差。尽管治疗方面取得了进展,但最佳治疗方法仍不明确。免疫检查点抑制剂与化疗联合使用时,已显示出改善患者预后的前景。
本研究旨在评估与单纯吉西他滨/顺铂(GC)相比,辅助使用替雷利珠单抗联合吉西他滨/顺铂(Tisle+GC)治疗高危MIUC患者的疗效和安全性。
我们对2016年10月至2023年3月期间在本中心接受治疗的117例经组织学确诊为pT3/4和pN+的MIUC患者进行了回顾性分析。符合条件的患者接受Tisle+GC或单纯GC治疗,排除那些先前接受过新辅助治疗的患者。我们使用Cox比例风险模型和Kaplan-Meier估计法比较了两组之间的无病生存期(DFS)、总生存期(OS)和治疗相关不良事件(AE)。
与GC组相比,Tisle+GC组的中位DFS(19.08个月对9.06个月,HR=0.114,p<0.001)和OS(20.07个月对10.63个月,HR=0.083,p=0.026)显著更长。神经束侵犯被确定为预后不良的重要预测因素(HR=22.1,p=0.003)。两组均经历了可控制的1-2级免疫相关AE,瘙痒最为常见,其次是肝功能异常和甲状腺功能紊乱。Tisle+GC组的非血液学毒性包括天冬氨酸转氨酶升高和低钠血症,而GC组主要报告呕吐。未发生与治疗相关的死亡。
在GC化疗中添加替雷利珠单抗显著改善了高危MIUC患者的DFS和OS。安全性可控,免疫相关AE可预测且不危及生命。这些发现支持Tisle+GC作为一种有效辅助治疗的潜力。
Tisle+GC是一种有前景的高危MIUC辅助治疗方法,可提高生存结局,安全性可控。需要进一步的前瞻性研究来证实这些结果,并确定这种联合治疗的长期益处。