首页> 美国卫生研究院文献>Current Controlled Trials in Cardiovascular Medicine >Open-label randomized multicentre phase II study to assess the efficacy and tolerability of sunitinib by dose administration regimen (dose modification or dose interruptions) in patients with advanced or metastatic renal cell carcinoma: study protocol of the SURF trial
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Open-label randomized multicentre phase II study to assess the efficacy and tolerability of sunitinib by dose administration regimen (dose modification or dose interruptions) in patients with advanced or metastatic renal cell carcinoma: study protocol of the SURF trial

机译:开放标签随机多中心II期研究通过剂量给药方案(剂量修改或剂量中断)评估舒尼替尼在晚期或转移性肾细胞癌患者中的疗效和耐受性:SURF试验的研究方案

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摘要

BackgroundSunitinib is a tyrosine kinase inhibitor approved in the first-line metastatic renal cell carcinoma (MRCC) setting at the dose of 50 mg daily for 4 weeks followed by a pause of 2 weeks. Due to toxicity, this standard schedule (50 mg daily 4/2) can induce up to 50% of sunitinib dose modification (reduction and/or interruption). The current recommendation in such case is to reduce the dose to 37.5 mg per day (standard schedule 4/2). Recent data highlight an alternative schedule: 2 weeks of treatment followed by 1 week of pause (experimental schedule 2/1). The SURF trial is set up to evaluate prospectively experimental schedule 2/1 when toxicity occurs. This article displays the key elements of the study protocol.
机译:背景舒尼替尼是一线转移性肾细胞癌(MRCC)设置中批准的酪氨酸激酶抑制剂,剂量为每天50 mg,持续4周,然后停顿2周。由于毒性,此标准时间表(每天4/2每天50 mg)可诱导高达50%的舒尼替尼剂量调整(减少和/或中断)。在这种情况下,当前的建议是将剂量减少到每天37.5 mg(标准计划4/2)。最新数据强调了另一种时间表:治疗2周,然后暂停1周(实验时间表2/1)。建立SURF试验是为了评估毒性发生时的前瞻性实验计划2/1。本文显示了研究方案的关键要素。

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