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Avelumab plus axitinib vs sunitinib for advanced renal cell carcinoma: Japanese subgroup analysis from JAVELIN Renal 101

机译:Avelumab加阿昔替尼与舒尼替尼治疗晚期肾细胞癌:来自JAVELIN Renal 101的日本亚组分析

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摘要

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.
机译:在未经治疗的晚期肾细胞癌(RCC)患者中进行avelumab +阿昔替尼vs舒尼替尼的JAVELIN Renal 101的3期试验证明,与舒尼替尼联合使用可显着改善无进展生存期(PFS)和更高的客观缓解率(ORR)。参加研究的日本患者(N = 67)被随机分配接受avelumab +阿昔替尼(N = 33)或舒尼替尼(N = 34); PD-L1 +肿瘤(免疫细胞≥1%)分别为67%和59%,国际转移性肾细胞癌数据库联合会(IMDC)有利/中度为6%/ 64%/ 27%vs 6%/ 82%/ 12% /不良的风险状态。在接受avelumab +阿昔替尼vs舒尼替尼治疗的患者中,PFS中位数(95%置信区间[CI])无法估计(8.1个月,不可估计)vs 11.2个月(1.6个月,不可估计)(危险比[HR]为0.49; PD-L1 +肿瘤患者的95%CI,0.152、1.563)和患者的16.6个月(8.1个月,不可估量)与11.2个月(4.2个月,不可估量)(HR,0.66; 95%CI,0.296,1.464)不论PD-L1表达如何。 PD-L1 +肿瘤患者的任一臂均未达到中位总生存期(OS),与PD-L1表达无关。无论PD-L1表达如何,患者的ORR(95%CI)为60.6%(42.1%,77.1%)对17.6%(6.8%,34.5%)。每只手臂的常见治疗紧急不良事件(所有级别;≥3级)分别为手足综合征(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 +阿昔替尼在未接受过治疗的日本RCC初治患者中有效且可耐受,这与总体人群的结果一致。

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