Department of Urology, Kurume University School of Medicine, Kurume, Japan
Department of Urology, Kurume University School of Medicine, Kurume, Japan.
Anticancer Res. 2024 Nov;44(11):5087-5093. doi: 10.21873/anticanres.17333.
BACKGROUND/AIM: Nivolumab and ipilimumab (NIVO+IPI) is standard therapy for patients with intermediate and poor risk advanced renal cell carcinoma (RCC). However, the efficacy and safety of NIVO+IPI in elderly patients aged >75 years remains unclear. This study aimed to determine the efficacy and safety of first-line NIVO+IPI treatment in patients aged >75 years with advanced RCC.
This study included 59 patients with advanced RCC who received NIVO+IPI as first-line therapy between September 2018 and December 2023. Objective response rates (ORRs), along with progression-free survival (PFS) and overall survival (OS) were compared between patients aged <75 years and ≥75 years, to assess survival outcomes.
A total of 46 (78.0%) and 13 (22.0%) patients were classified into <75 years and ≥75 years groups, respectively, at NIVO+IPI initiation. The ORRs were 45.7% for <75 years and 53.8% for ≥75 years (p=0.2422). No significant differences in PFS (p=0.0729) were observed between groups. In contrast, patients aged ≥75 years had better OS than those aged <75 years (p=0.0212). However, no significant difference was observed in the OS between the two groups of patients with clear cell histology (p=0.0532). The incidence of immune-related adverse events higher than Grade 3 was not significantly different between the two groups (p=0.5016).
NIVO and IPI combination therapy is both safe and efficacious in patients aged ≥75 years with advanced RCC.
背景/目的:纳武利尤单抗和伊匹单抗(NIVO+IPI)是中危和高危晚期肾细胞癌(RCC)患者的标准治疗方法。然而,NIVO+IPI 在 >75 岁老年患者中的疗效和安全性尚不清楚。本研究旨在确定 NIVO+IPI 一线治疗>75 岁晚期 RCC 患者的疗效和安全性。
本研究纳入了 59 例接受 NIVO+IPI 一线治疗的晚期 RCC 患者,这些患者的治疗时间为 2018 年 9 月至 2023 年 12 月。比较了年龄<75 岁和≥75 岁患者的客观缓解率(ORR)、无进展生存期(PFS)和总生存期(OS),以评估生存结局。
NIVO+IPI 起始时,患者被分为<75 岁组(46 例,78.0%)和≥75 岁组(13 例,22.0%)。<75 岁组的 ORR 为 45.7%,≥75 岁组为 53.8%(p=0.2422)。两组的 PFS 无显著差异(p=0.0729)。相反,≥75 岁组患者的 OS 优于<75 岁组(p=0.0212)。然而,在透明细胞组织学患者中,两组的 OS 无显著差异(p=0.0532)。两组患者发生>3 级免疫相关不良事件的发生率无显著差异(p=0.5016)。
NIVO 和 IPI 联合治疗对>75 岁晚期 RCC 患者安全且有效。