Nemoto Yuki, Endo Takanori, Segawa Hogara, Nakamura Kazutaka, Nishimura Koichi, Horiuchi Toshihide, Toki Daisuke, Kobayashi Hirohito, Takagi Toshio, Kondo Tsunenori
Department of Urology, Tokyo Women's Medical University Adachi Medical Center, 4-33-1 Kohoku, Adachi, Tokyo, Japan.
Department of Urology, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo, Japan.
Int Urol Nephrol. 2025 Apr 10. doi: 10.1007/s11255-025-04486-2.
To clarify the efficacy and safety profile of nivolumab plus cabozantinib combination therapy in advanced renal cell carcinoma patients older than 80 years.
We retrospectively evaluated 42 patients with advanced renal cell carcinoma treated with nivolumab plus cabozantinib as the first-line therapy at our institution. The patients were categorized according to age as those aged ≥ 80 years and those aged < 80 years. Efficacy was analysed by comparing the progression-free survival, overall survival, objective response rate, and disease control rate between the two groups. Safety was assessed by comparing the incidence of adverse events.
Ten patients (31%) were classified as age ≥ 80 group. No significant differences were observed in the progression-free survival (p = 0.682), the overall survival (p = 0.627), objective response rate (p = 0.195), and disease control rate (p = 0.070) between the two groups. There was no significant difference in the incidence of all grades of adverse events(p = 1.000), but there was a trend toward a higher incidence of grade 3 or higher adverse events in the group of patients aged < 80 years (p = 0.066).
The efficacy and safety of nivolumab plus cabozantinib combination therapy were comparable between the patients aged ≥ 80 years and those aged < 80 years. Thus, chronological age alone is not a contraindication for nivolumab plus cabozantinib combination therapy for advanced renal cell carcinoma.
阐明纳武利尤单抗联合卡博替尼治疗80岁以上晚期肾细胞癌患者的疗效和安全性。
我们回顾性评估了42例在我院接受纳武利尤单抗联合卡博替尼一线治疗的晚期肾细胞癌患者。根据年龄将患者分为≥80岁组和<80岁组。通过比较两组的无进展生存期、总生存期、客观缓解率和疾病控制率来分析疗效。通过比较不良事件的发生率来评估安全性。
10例患者(31%)被归类为年龄≥80岁组。两组之间在无进展生存期(p = 0.682)、总生存期(p = 0.627)、客观缓解率(p = 0.195)和疾病控制率(p = 0.070)方面未观察到显著差异。所有级别的不良事件发生率无显著差异(p = 1.000),但<80岁患者组3级或更高级别不良事件的发生率有升高趋势(p = 0.066)。
纳武利尤单抗联合卡博替尼治疗在≥80岁和<80岁患者中的疗效和安全性相当。因此,仅按年龄计算并非晚期肾细胞癌患者接受纳武利尤单抗联合卡博替尼治疗的禁忌证。