Department of Urology, Osaka University Graduate School of Medicine, Osaka, Japan.
Department of Urology, Department of Molecular Oncology, Niigata University Graduate School of Medicine, Niigata, Japan.
Cancer Sci. 2020 Mar;111(3):907-923. doi: 10.1111/cas.14294. Epub 2020 Feb 5.
The phase 3 JAVELIN Renal 101 trial of avelumab + axitinib vs sunitinib in patients with treatment-naive advanced renal cell carcinoma (RCC) demonstrated significantly improved progression-free survival (PFS) and higher objective response rate (ORR) with the combination vs sunitinib. Japanese patients enrolled in the study (N = 67) were randomized to receive avelumab + axitinib (N = 33) or sunitinib (N = 34); 67% vs 59% had PD-L1+ tumors (≥1% of immune cells) and 6%/64%/27% vs 6%/82%/12% had International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) favorable/intermediate/poor risk status. In patients who received avelumab + axitinib vs sunitinib, median PFS (95% confidence interval [CI]) was not estimable (8.1 months, not estimable) vs 11.2 months (1.6 months, not estimable) (hazard ratio [HR], 0.49; 95% CI, 0.152, 1.563) in patients with PD-L1+ tumors and 16.6 months (8.1 months, not estimable) vs 11.2 months (4.2 months, not estimable) (HR, 0.66; 95% CI, 0.296, 1.464) in patients irrespective of PD-L1 expression. Median overall survival (OS) has not been reached in either arm in patients with PD-L1+ tumors and irrespective of PD-L1 expression. ORR (95% CI) was 60.6% (42.1%, 77.1%) vs 17.6% (6.8%, 34.5%) in patients irrespective of PD-L1 expression. Common treatment-emergent adverse events (all grade; grade ≥3) in each arm were hand-foot syndrome (64%; 9% vs 71%; 9%), hypertension (55%; 30% vs 44%; 18%), hypothyroidism (55%; 0% vs 24%; 0%), dysgeusia (21%; 0% vs 56%; 0%) and platelet count decreased (3%; 0% vs 65%; 32%). Avelumab + axitinib was efficacious and tolerable in treatment-naive Japanese patients with advanced RCC, which is consistent with results in the overall population.
三期 JAVELIN Renal 101 试验比较了avelumab+axitinib 与 sunitinib 一线治疗初治晚期肾细胞癌(RCC)的疗效,结果显示联合用药较 sunitinib 显著改善了无进展生存期(PFS),并提高了客观缓解率(ORR)。该研究纳入了日本患者(N=67),随机接受avelumab+axitinib(N=33)或 sunitinib(N=34)治疗;67%的患者肿瘤 PD-L1 阳性(≥1%免疫细胞),6%/64%/27%vs 6%/82%/12%的患者国际转移性肾细胞癌数据库联盟(IMDC)预后良好/中等/不良。在 PD-L1 阳性肿瘤患者中,avelumab+axitinib 组 vs sunitinib 组中位 PFS(95%置信区间[CI])无估计值(8.1 个月,无估计值)vs 11.2 个月(1.6 个月,无估计值)(风险比[HR],0.49;95%CI,0.152,1.563),PD-L1 阴性肿瘤患者中位 PFS 分别为 16.6 个月(8.1 个月,无估计值)和 11.2 个月(4.2 个月,无估计值)(HR,0.66;95%CI,0.296,1.464)。在无论 PD-L1 表达情况如何的患者中,avelumab+axitinib 组和 sunitinib 组均未达到中位总生存期(OS)。无论 PD-L1 表达情况如何,ORR(95%CI)分别为 60.6%(42.1%,77.1%)和 17.6%(6.8%,34.5%)。每个治疗组中常见的治疗相关不良事件(所有等级;≥3 级)包括手足综合征(64%;9%vs 71%;9%)、高血压(55%;30%vs 44%;18%)、甲状腺功能减退(55%;0%vs 24%;0%)、味觉障碍(21%;0%vs 56%;0%)和血小板计数减少(3%;0%vs 65%;32%)。Avelumab+axitinib 在治疗初治的日本晚期 RCC 患者中具有疗效和可耐受性,与总体人群的结果一致。