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Nivolumab for the Treatment of Patients with Metastatic Non-Clear Cell Renal Cell Carcinoma (nccRCC): A Single-Institutional Experience and Literature Meta-Analysis

机译:Nivolumab用于治疗转移性非透明细胞肾细胞癌(NCCRCC)的患者:单一制度经验和文献荟萃分析

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Introduction Nivolumab alone and in combination with ipilimumab is approved for the treatment of patients with metastatic renal cell carcinoma (RCC) who received prior vascular endothelial growth factor receptor tyrosine kinase inhibitors (VEGFR-TKI) and those who are treatment naive, respectively. However, the clinical activity of nivolumab in non-clear cell RCC (nccRCC) is unknown, as these patients were excluded from the trials. Materials and Methods We reviewed the records of patients who received nivolumab for nccRCC and ccRCC with 20% rhabdoid with the primary endpoint to assess the objective response rate (ORR). We assessed radiographic response using RECIST, v1.1. Secondary endpoints were progression-free survival (PFS) and overall survival (OS). We also reviewed the literature to identify studies reporting on the clinical activity of immune checkpoint inhibitors in nccRCC, and performed a meta-analysis of proportions for ORR and disease control rate (DCR). Results Twelve patients (30%) had papillary histology, 11 (27.5%) had unclassified, 8 (20%) had ccRCC with rhabdoid component, 5 (12.5%) had chromophobe, 3 (7.5%) had translocation, and 1 (2.5%) had mucinous tubular and spindle cell carcinoma. Overall, seven patients (21.6%, 95% confidence interval [CI], 8.7%–37.9%) had an objective response, including three patients (8.8%, 95% confidence interval [CI], 1.9%–23.7%) who achieved a complete remission. At a median follow-up of 24.5 monoths (95% CI, 17.7–32.6), median PFS was 4.9 monoths (95% CI, 3.53–10.27) and median OS was 21.7 monoths (95% CI, 7.83 mo to not reached). There were no treatment-related deaths. We also identified two retrospective studies reporting best ORR in patients with nccRCC receiving PD-1/PD-L1 checkpoint blockade. The ORR and DCR for the total cohort were, respectively, 18.6% (95% CI, 11.9%–26.4%) and 53.4% (95% CI, 44.2%–62.5%). Conclusion Nivolumab demonstrated activity in unclassified nccRCC and ccRCC with 20% rhabdoid; further randomized clinical trials are warranted. Implications for Practice This article reports on the clinical activity and safety of immune checkpoint inhibitors in non-clear cell kidney cancer. The retrospective data with the meta-analysis provides a summary that will help guide the treatment of this rare and heterogeneous group of kidney cancers.
机译:仅介绍Nivolumab和与Ipilimumab的组合被批准用于治疗接受先前血管内皮生长因子受体酪氨酸激酶抑制剂(VEGFR-TKI)的转移性肾细胞癌(RCC)和治疗幼稚的患者。然而,非透明细胞RCC(NCCRCC)中Nivolumab的临床活性是未知的,因为这些患者被排除在试验中。材料和方法我们审查了接受NCCRMAB的NCCRUMAB和CCRCC的患者的记录,其中20%Rhabdoid与主要终点,以评估客观反应率(ORR)。我们使用Recist V1.1评估了射线照相响应。次要终点是无进展的存活率(PFS)和总存活(OS)。我们还审查了鉴定了关于NCCRCC中免疫检查点抑制剂临床活性的研究,并对ORR和疾病控制率的比例进行了荟萃分析的研究。结果12名患者(30%)具有乳头状组织学,11名(27.5%)未分类,8(20%)具有Rhabdoid组分的CCRCC,5(12.5%)具有致铬,3(7.5%)易位,1(2.5 %)具有粘液管和主轴细胞癌。总体而言,7名患者(21.6%,95%置信区间[CI],8.7%-37.9%)具有客观反应,其中包括三名患者(8.8%,95%置信区间[CI],1.9%-23.7%)达成完全缓解。在24.5分钟的中间后续行动中(95%CI,17.7-32.6),中位数PFS为4.9分(95%CI,3.53-10.27)和中位数操作系统是21.7个单门(95%CI,7.83 MO无法达到) 。没有治疗有关的死亡。我们还确定了两项回顾性研究,报告了NCCRCC接收PD-1 / PD-L1检查点延迟的NCCRCC患者的最佳ORR。总群组的ORR和DCR分别为18.6%(95%CI,11.9%-26.4%和53.4%(95%CI,44.2%-62.5%)。结论Nivolumab在未分类的NCCRCC和CCRCC中表现出具有&gt的活性; 20%Rhabdoid;需要进一步随机临床试验。本文对实践的影响本文报告了非透明细胞肾癌中免疫检查点抑制剂的临床活性和安全性。具有Meta-Analysis的回顾性数据提供了一个摘要,可以帮助指导这种稀有和异质肾癌组的治疗。

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