Department of Urology, Jichi Medical University Saitama Medical Center, 1-847, Amanuma-cho, Omiya-ku, Saitama, Saitama, 330-8503, Japan.
Musashino Study Group, Saitama, Japan.
Int J Clin Oncol. 2023 Dec;28(12):1651-1658. doi: 10.1007/s10147-023-02406-x. Epub 2023 Sep 2.
Immune-related adverse events (irAEs) in patients treated with immune check inhibitors are associated with favourable response rate and survivals in multiple cancers, including renal cell carcinoma (RCC). The aim of this study was to investigate how irAEs were associated with improved survivals in advanced RCC patients treated with nivolumab plus ipilimumab.
This retrospective study included patients who received nivolumab plus ipilimumab at six centres, institutions, or hospitals between September 2018 and February 2022. We assessed associations of the development and the number of irAEs with overall survival (OS) and progression-free survival (PFS). To eliminate immortal time bias, landmark analysis and a Cox model with time-dependent variables were used.
This study included 129 patients with a median follow-up of 12.3 months. The 2-year OS and PFS rates were 55% and 42%, respectively. Ninety six patients experienced irAEs. The development of irAEs was positively associated with OS and PFS rates (hazard ratio [HR] 0.328, 95% confidence interval [CI] 0.165-0.648, p = 0.001; HR 0.334, 95% CI 0.151-0.737, p = 0.007). Patients who experienced multiple irAEs had longer OS (HR 0.507, 95% CI 0.235-1.097, p = 0.085 or HR 0.245, 95% CI 0.110-0.544, p < 0.001) and PFS (HR 0.572, 95% CI 0.316-1.036, p = 0.085 or HR 0.267, 95% CI 0.113-0.628, p = 0.002) compared with those who experienced single or zero irAE.
Developing irAEs, particularly multiple irAEs, is associated with favourable survivals in advanced RCC patients treated with nivolumab plus ipilimumab.
在接受免疫检查点抑制剂治疗的患者中,免疫相关不良事件(irAEs)与多种癌症(包括肾细胞癌[RCC])的高反应率和存活率相关。本研究的目的是调查 irAEs 如何与接受纳武利尤单抗联合伊匹单抗治疗的晚期 RCC 患者的生存改善相关。
本回顾性研究纳入了 2018 年 9 月至 2022 年 2 月期间在六个中心、机构或医院接受纳武利尤单抗联合伊匹单抗治疗的患者。我们评估了 irAEs 的发生和数量与总生存期(OS)和无进展生存期(PFS)的相关性。为消除不朽时间偏差,使用了 landmark 分析和具有时间依赖性变量的 Cox 模型。
本研究纳入了 129 名患者,中位随访时间为 12.3 个月。2 年 OS 和 PFS 率分别为 55%和 42%。96 名患者出现 irAEs。irAEs 的发生与 OS 和 PFS 率呈正相关(风险比[HR]0.328,95%置信区间[CI]0.165-0.648,p=0.001;HR 0.334,95%CI 0.151-0.737,p=0.007)。发生多种 irAEs 的患者 OS 更长(HR 0.507,95%CI 0.235-1.097,p=0.085 或 HR 0.245,95%CI 0.110-0.544,p<0.001)和 PFS(HR 0.572,95%CI 0.316-1.036,p=0.085 或 HR 0.267,95%CI 0.113-0.628,p=0.002)与发生单一或零 irAE 的患者相比。
在接受纳武利尤单抗联合伊匹单抗治疗的晚期 RCC 患者中,发生 irAEs,特别是多种 irAEs,与有利的生存相关。