Plimack Elizabeth R, Powles Thomas, Stus Viktor, Gafanov Rustem, Nosov Dmitry, Waddell Tom, Alekseev Boris, Pouliot Frédéric, Melichar Bohuslav, Soulières Denis, Borchiellini Delphine, McDermott Raymond S, Vynnychenko Ihor, Chang Yen-Hwa, Tamada Satoshi, Atkins Michael B, Li Chenxiang, Perini Rodolfo, Molife L Rhoda, Bedke Jens, Rini Brian I
Fox Chase Cancer Center, Philadelphia, PA, USA.
Barts Health NHS Trust and the Royal Free NHS Foundation Trust, Barts Cancer Institute, London, UK; Queen Mary University of London, London, UK.
Eur Urol. 2023 Nov;84(5):449-454. doi: 10.1016/j.eururo.2023.06.006. Epub 2023 Jul 25.
Previous analyses of KEYNOTE-426, an open-label, phase 3 randomized study, showed superior efficacy of first-line pembrolizumab plus axitinib to sunitinib in advanced clear cell renal cell carcinoma (ccRCC). We report results of the final protocol-prespecified analysis of KEYNOTE-426. Patients received pembrolizumab 200 mg intravenously every 3 wk plus axitinib 5 mg orally twice daily or sunitinib 50 mg orally once daily (4 wk per 6-wk cycle). The dual primary endpoints were overall survival (OS) and progression-free survival (PFS) as per RECIST v1.1 by a blinded independent central review. The secondary endpoints included objective response rate (ORR) and duration of response (DOR). The median study follow-up was 43 (range, 36-51) mo. Benefit with pembrolizumab plus axitinib versus sunitinib was maintained for OS (hazard ratio [HR], 0.73 [95% confidence interval {CI}, 0.60-0.88]), PFS (HR, 0.68 [95% CI, 0.58-0.80]), and ORR (60% vs 40%). The median DOR was 24 (range, 1.4+ to 43+) versus 15 (range, 2.3-43+) mo in the pembrolizumab plus axitinib versus the sunitinib arm. No new safety signals emerged. These results support pembrolizumab plus axitinib as a standard of care for patients with previously untreated advanced ccRCC. PATIENT SUMMARY: Extended results of KEYNOTE-426 support pembrolizumab plus axitinib as the standard of care for advanced clear cell renal cell carcinoma.
KEYNOTE-426是一项开放标签的3期随机研究,此前对该研究的分析表明,在晚期肾透明细胞癌(ccRCC)中,一线帕博利珠单抗联合阿昔替尼的疗效优于舒尼替尼。我们报告了KEYNOTE-426最终方案预设分析的结果。患者接受每3周静脉注射200 mg帕博利珠单抗联合每日口服两次5 mg阿昔替尼,或每日口服一次50 mg舒尼替尼(每6周周期为4周)。双重主要终点为根据RECIST v1.1由独立盲态中央审查评估的总生存期(OS)和无进展生存期(PFS)。次要终点包括客观缓解率(ORR)和缓解持续时间(DOR)。研究的中位随访时间为43(范围36 - 51)个月。帕博利珠单抗联合阿昔替尼对比舒尼替尼在OS(风险比[HR],0.73[95%置信区间{CI},0.60 - 0.88])、PFS(HR,0.68[95%CI,0.58 - 0.80])和ORR(60%对40%)方面的获益得以维持。帕博利珠单抗联合阿昔替尼组的中位DOR为24(范围,1.4 +至43 +)个月,而舒尼替尼组为15(范围,2.3 - 43 +)个月。未出现新的安全信号。这些结果支持帕博利珠单抗联合阿昔替尼作为既往未治疗的晚期ccRCC患者的标准治疗方案。患者总结:KEYNOTE-426的扩展结果支持帕博利珠单抗联合阿昔替尼作为晚期肾透明细胞癌的标准治疗方案。