Wang Qian, Zhang Xingming, Zhu Qiyu, Zeng Hong, Dai Jindong, Chen Junru, Zhao Jinge, Sun Guangxi, Liu Zhenhua, Zeng Hao, Shen Pengfei
Department of Urology, Institute of Urology, West China Hospital, Sichuan University, No.37 Guoxue Alley, Wuhou District, Chengdu, 610041, Sichuan, People's Republic of China.
Int Urol Nephrol. 2025 May;57(5):1433-1440. doi: 10.1007/s11255-024-04344-7. Epub 2024 Dec 24.
To evaluate the efficacy and safety of extended immunotherapy in first-line immune checkpoint inhibitors (ICIs)-tyrosine kinase inhibitors (TKIs) combination treatment for advanced renal cell carcinoma (RCC).
We retrospectively analyzed data from patients with advanced RCC who received first-line ICIs-TKIs combination treatment at West China Hospital of Sichuan University between October 2018 and July 2024. Patients who are assessed as having a disease control status after 2 years of continuous treatment will continue to receive immune checkpoint inhibitors until the inhibitors are discontinued due to disease progression or death.
A total of 86 patients were screened and 14 patients diagnosed with clear cell RCC (ccRCC) were enrolled. After 65 months of follow-up, three-year progression-free survival (PFS) rate was 71.4% and 4 year PFS rate was 59.5%. The 5 year overall survival (OS) rate was 58.3%. During extended treatment, one patient (7.1%) experienced a transition from stable disease (SD) to partial response (PR) and two patients (14.3%) experienced a transition from PR to complete response (CR). The best tumor shrinkage rates presenting after 24 months had longer PFS and OS compared to those presenting within 24 months (median PFS: not reached vs. 36 months; Hazard Ratio (HR) = 0.10, 95% CI 0.01-0.80, P = 0.03). For safety, extended immunotherapy did not increase treatment-related toxicities compared to safety profile before 24 months.
Our analysis of real-world data indicates that patients with extended immunotherapy after 24 months had potential survival benefits and manageable toxicity. Large-scale, prospective studies are still needed to further verify the conclusion.
评估延长免疫治疗在晚期肾细胞癌(RCC)一线免疫检查点抑制剂(ICIs)-酪氨酸激酶抑制剂(TKIs)联合治疗中的疗效和安全性。
我们回顾性分析了2018年10月至2024年7月在四川大学华西医院接受一线ICIs-TKIs联合治疗的晚期RCC患者的数据。连续治疗2年后评估为疾病控制状态的患者将继续接受免疫检查点抑制剂治疗,直至因疾病进展或死亡而停药。
共筛选出86例患者,14例诊断为透明细胞RCC(ccRCC)的患者入组。经过65个月的随访,三年无进展生存期(PFS)率为71.4%,四年PFS率为59.5%。五年总生存期(OS)率为58.3%。在延长治疗期间,1例患者(7.1%)经历了从疾病稳定(SD)到部分缓解(PR)的转变,2例患者(14.3%)经历了从PR到完全缓解(CR)的转变。24个月后出现的最佳肿瘤缩小率与24个月内出现的相比,PFS和OS更长(中位PFS:未达到 vs. 36个月;风险比(HR)=0.10,95%置信区间0.01-0.80,P=0.03)。在安全性方面,与24个月前的安全性相比,延长免疫治疗并未增加治疗相关毒性。
我们对真实世界数据的分析表明,24个月后接受延长免疫治疗的患者具有潜在的生存获益且毒性可控。仍需要大规模的前瞻性研究来进一步验证该结论。