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首页> 外文期刊>Cancer science. >Avelumab plus axitinib vs sunitinib for advanced renal cell carcinoma: Japanese subgroup analysis from JAVELIN Renal 101
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Avelumab plus axitinib vs sunitinib for advanced renal cell carcinoma: Japanese subgroup analysis from JAVELIN Renal 101

机译:Avelumab Plus Axitinib VS Sunitinib用于晚期肾细胞癌:Jault Javelin Renal 101的亚组分析

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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:Avelumab的第3阶段标准刺激肾101试验Avelumabα+?Axitinib对治疗幼稚肾细胞癌(RCC)的患者的Akitinib Vs Sunitinib表现出显着改善的无进展生存(PFS)和更高的客观反应率(ORR)与组合VS桑蒂尼。在研究中注册的日本患者(n?=Δ67)被随机接受Avelumab?+ +?axitinib(n?= 33)或unitinib(n?=?34); 67%Vs 59%具有PD-L1 +肿瘤(≥1%的免疫细胞),6%/ 64%/ 27%与6%/ 82%/ 12%有国际转移性肾细胞癌数据库联盟(IMDC)有利/中级/风险状况不佳。在接受Avelumab的患者中,Axitinib VS Sunitinib,中值PFS(95%置信区间[CI])不是估计(8.1?月,而不是估计)与11.2?月(1.6?月,不是估计)(危险比[ HR],0.49; 95%CI,0.152,1.563)在PD-L1 +肿瘤的患者中,16.6个月(8.1?月,不是估计)与11.2?月份(4.2?月,不是估计)(HR,0.66; 95患者中%CI,0.296,1.464)与PD-L1表达无关。在PD-L1 +肿瘤的患者中,尚未达到中位整体存活(OS),无论pD-L1表达如何,都没有达到任何臂。无论PD-L1表达如何,ORR(95%CI)为60.6%(42.1%,77.1%)与17.6%(6.8%,34.5%)。每只臂中的常见治疗 - 紧急不良事件(所有等级;≥3)是手足综合征(64%; 9%vs 71%; 9%),高血压(55%; 30%vs 44%; 18% ),甲状腺功能减退症(55%; 0%vs 24%; 0%),痢疾乌西亚(21%; 0%vs 56%; 0%)和血小板计数下降(3%; 0%vs 65%; 32%)。 Avelumab?+?Axitinib在治疗幼稚的高级RCC患者中有效和可耐受,这与整体人口的结果一致。

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