首页> 外文期刊>The lancet oncology >Nivolumab monotherapy in recurrent metastatic urothelial carcinoma (CheckMate 032): a multicentre, open-label, two-stage, multi-arm, phase 1/2 trial
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Nivolumab monotherapy in recurrent metastatic urothelial carcinoma (CheckMate 032): a multicentre, open-label, two-stage, multi-arm, phase 1/2 trial

机译:Nivolumab单药治疗复发性转移性尿路上皮癌(CheckMate 032):一项多中心,开放标签,两阶段,多组,1/2期试验

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Background Few effective treatments exist for patients with advanced urothelial carcinoma that has progressed after platinum-based chemotherapy. We assessed the activity and safety of nivolumab in patients with locally advanced or metastatic urothelial carcinoma whose disease progressed after previous platinum-based chemotherapy. Methods In this phase 1/2, multicentre, open-label study, we enrolled patients (age >= 18 years) with urothelial carcinoma of the renal pelvis, ureter, bladder, or urethra at 16 sites in Finland, Germany, Spain, the UK, and the USA. Patients were not selected by PD-L1 expression, but tumour PD-L1 membrane expression was assessed retrospectively. Patients received nivolumab 3 mg/kg intravenously every 2 weeks until disease progression or treatment discontinuation because of unacceptable toxicity or other protocol-defined reasons, whichever occurred later. The primary endpoint was objective response by investigator assessment. All patients who received at least one dose of the study drug were included in the analyses. We report an interim analysis of this ongoing trial. CheckMate 032 is registered with ClinicalTrials.gov, NCT01928394.
机译:背景技术铂类化学疗法治疗后进展的晚期尿路上皮癌患者几乎没有有效的治疗方法。我们评估了nivolumab在局部晚期或转移性尿路上皮癌患者中的活性和安全性,这些患者的病情在先前的铂类化疗后有所进展。方法在这一1/2阶段,多中心,开放标签的研究中,我们在芬兰,德国,西班牙,美国,美国和欧洲的16个地方招募了肾盂,输尿管,膀胱或尿道的尿路上皮癌患者(年龄> = 18岁)。英国和美国。未通过PD-L1表达选择患者,但回顾性评估了肿瘤PD-L1膜表达。患者每2周静脉注射3 mg / kg的nivolumab,直到由于不可接受的毒性或其他方案定义的原因(以较迟发生为准),疾病进展或治疗中止。主要终点是研究者评估的客观反应。所有接受至少一剂研究药物的患者均纳入分析。我们报告了该正在进行的试验的中期分析。 CheckMate 032已在ClinicalTrials.gov(NCT01928394)中注册。

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