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首页> 外文期刊>The New England journal of medicine >Pembrolizumab plus Axitinib versus Sunitinib for Advanced Renal-Cell Carcinoma
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Pembrolizumab plus Axitinib versus Sunitinib for Advanced Renal-Cell Carcinoma

机译:Pembrolizumab Plus Axitinib与unitinib进行晚期肾细胞癌

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摘要

Background The combination of pembrolizumab and axitinib showed antitumor activity in a phase 1b trial involving patients with previously untreated advanced renal-cell carcinoma. Whether pembrolizumab plus axitinib would result in better outcomes than sunitinib in such patients was unclear. Methods In an open-label, phase 3 trial, we randomly assigned 861 patients with previously untreated advanced clear-cell renal-cell carcinoma to receive pembrolizumab (200 mg) intravenously once every 3 weeks plus axitinib (5 mg) orally twice daily (432 patients) or sunitinib (50 mg) orally once daily for the first 4 weeks of each 6-week cycle (429 patients). The primary end points were overall survival and progression-free survival in the intention-to-treat population. The key secondary end point was the objective response rate. All reported results are from the protocol-specified first interim analysis. Results After a median follow-up of 12.8 months, the estimated percentage of patients who were alive at 12 months was 89.9% in the pembrolizumab-axitinib group and 78.3% in the sunitinib group (hazard ratio for death, 0.53; 95% confidence interval [CI], 0.38 to 0.74; P<0.0001). Median progression-free survival was 15.1 months in the pembrolizumab-axitinib group and 11.1 months in the sunitinib group (hazard ratio for disease progression or death, 0.69; 95% CI, 0.57 to 0.84; P<0.001). The objective response rate was 59.3% (95% CI, 54.5 to 63.9) in the pembrolizumab-axitinib group and 35.7% (95% CI, 31.1 to 40.4) in the sunitinib group (P<0.001). The benefit of pembrolizumab plus axitinib was observed across the International Metastatic Renal Cell Carcinoma Database Consortium risk groups (i.e., favorable, intermediate, and poor risk) and regardless of programmed death ligand 1 expression. Grade 3 or higher adverse events of any cause occurred in 75.8% of patients in the pembrolizumab-axitinib group and in 70.6% in the sunitinib group. Conclusions Among patients with previously untreated advanced renal-cell carcinoma, treatment with pembrolizumab plus axitinib resulted in significantly longer overall survival and progression-free survival, as well as a higher objective response rate, than treatment with sunitinib.
机译:背景技术Pembrozumab和Axitinib的组合在涉及先前未经处理的晚期肾细胞癌的患者的患者中显示抗肿瘤活性。 Pembrolizumab Plus Axitinib是否会导致比Sunitinib在这些患者中更好的结果尚不清楚。方法在开放标签,第3阶段试验中,我们随机分配了861例以前未经处理的先进的晚期透明细胞肾细胞癌,每3周每天每天口服每3周(5毫克)静脉内静脉注射(200mg)(432患者)或每日6周周期的前4周(429名患者)的每日晒锡(50毫克)。主要终点在意向治疗人群中是整体存活和无进展的生存期。关键次要终点是客观响应率。所有报告的结果都来自协议 - 指定的第一个临时分析。结果后续12.8个月后,彭布罗齐妥昔替尼(Sunitinib组)在12个月内活跃的患者的估计百分比为89.9%(死亡危险比,0.53; 95%的置信区间[Ci],0.38至0.74; p <0.0001)。在Pembrolizumab-Axitinib组中,中位进展生存率为15.1个月,在Sunitinib组(疾病进展或死亡的危险比)的11.1个月内为11.1个月,0.69%; 95%CI,0.57至0.84; p <0.001)。目标反应率为Pembolizumab-Axitinib组的59.3%(95%CI,54.5至63.9),在Sunitinib组中为35.7%(95%CI,31.1至40.4)(P <0.001)。在国际转移性肾细胞癌数据库(即,有利,中级,风险不良)和无论编程死亡配体1表达如何,观察到彭布洛齐氏肾小球癌的益处。在彭布洛拉-Axitinib组的75.8%的患者中,任何原因的3级或更高的不良事件发生在户75.8%的患者中。结论以前未经治疗的先进肾细胞癌的患者,用Pembrolizumab Plus Axitinib治疗导致总生存率和无进展的生存率显着更长,以及较高的客观反应率,而不是与日光尼治疗。

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