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首页> 外文期刊>Journal of Clinical Oncology >Safety and Efficacy of Nivolumab in Brain Metastases From Renal Cell Carcinoma: Results of the GETUG-AFU 26 NIVOREN Multicenter Phase II Study
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Safety and Efficacy of Nivolumab in Brain Metastases From Renal Cell Carcinoma: Results of the GETUG-AFU 26 NIVOREN Multicenter Phase II Study

机译:Nivolumab在肾细胞癌脑转移中的安全性和有效性:Getug-AFU 26 Nivoren Muvoren Muids II研究的结果

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摘要

PURPOSENivolumab is standard of care for patients with metastatic clear cell renal cell carcinoma (ccRCC) after failure of antiangiogenic therapies, but its activity on brain metastases from ccRCC remains unknown, because these patients were excluded from pivotal studies. We aimed to assess the activity of nivolumab in this population.METHODSThe GETUG-AFU 26 NIVOREN phase II trial assessed the activity and safety of nivolumab in patients with metastatic ccRCC who failed vascular endothelial growth factor-directed therapies (ClinicalTrials.gov identifier: NCT03013335). Patients with asymptomatic brain metastases were prospectively identified and underwent dedicated brain evaluation. Two cohorts were constituted: cohort A comprised patients with previously untreated brain metastases, and cohort B comprised patients whose brain metastases underwent prior therapy. The primary end point was intracranial response rate in cohort A.RESULTSSeventy-three patients with brain metastases were included: 39 in cohort A and 34 in cohort B. Intracranial response rate was 12% in cohort A; no objective response was reported in patients with brain lesions that were multiple or larger than 1 cm. Median intracranial progression-free survival was 2.7 months (95% CI, 2.3 to 4.6 months) in cohort A and 4.8 months (95% CI, 3.0 to 8.0 months) in cohort B, with adjusted hazard ratio of 2.04 (95% CI, 1.08 to 3.83). Overall survival rate at 12 months was 67% (95% CI, 49.6% to 79.1%) in cohort A and 59% (95% CI, 40.6% to 73.2%) in cohort B. Most patients in cohort A (72%) needed subsequent focal brain therapy. Nivolumab was well tolerated, with no unexpected toxicity.CONCLUSIONNivolumab activity is limited in patients with untreated brain metastases from ccRCC. Brain imaging and focal therapy should be considered before immune checkpoint inhibitors in patients with metastatic ccRCC.
机译:Purposenivolumab是抗血管生成治疗失败后转移性透明细胞肾细胞癌(CCRCC)的护理标准,但其对来自CCRCC的脑转移的活性仍然未知,因为这些患者被排除在枢轴研究之外。我们的目标是评估本群体中Nivolumab的活性.TheDsthe Getug-AFU 26 Nivoren第二阶段试验评估了血管内皮生长因子导向治疗失败的血管性CCRCC患者中Nivolumab的活性和安全性(Clinicaltrials.gov标识符:NCT03013335) 。患有无症状脑转移的患者进行了前瞻性鉴定和接受了专用脑评估。构成了两个群组:群组A包含以前未经治疗的脑转移患者,队列B包括脑转移的患者在前治疗。主要终点是群组A.Resultsseventy-3患者的颅内反应率包括:39群队列A和34中的群组中的颈腹响应率为12%;在脑病变的患者中没有报道无客观反应,其多于1厘米或大于1厘米。中位数颅内进展生存率为2.7个月(95%CI,2.3至4.6个月),群组B和4.8个月(95%CI,3.0至8.0个月),调整后危险比为2.04(95%CI, 1.08至3.83)。 12个月的整体生存率为67%(95%CI,49.6%至79.1%,49.6%至79.1%)在群组B.群组中的大多数患者A(72%)需要随后的焦平脑治疗。 Nivolumab耐受良好,没有意外的毒性。来自CCRCC未经处理的脑转移患者的患者,无意识的毒性。在转移CCRCC患者的免疫检查点抑制剂之前,应考虑脑成像和焦点治疗。

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