首页> 美国卫生研究院文献>Journal of Clinical Oncology >Efficacy and Tolerability of First-Line Cetuximab Plus Leucovorin Fluorouracil and Oxaliplatin (FOLFOX-4) Versus FOLFOX-4 in Patients With RAS Wild-Type Metastatic Colorectal Cancer: The Open-Label Randomized Phase III TAILOR Trial
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Efficacy and Tolerability of First-Line Cetuximab Plus Leucovorin Fluorouracil and Oxaliplatin (FOLFOX-4) Versus FOLFOX-4 in Patients With RAS Wild-Type Metastatic Colorectal Cancer: The Open-Label Randomized Phase III TAILOR Trial

机译:一线西妥昔单抗联合白细胞素氟尿嘧啶和奥沙利铂(FOLFOX-4)与FOLFOX-4在RAS野生型转移性结直肠癌患者中的疗效和耐受性:开放标签随机III期TAILOR试验

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摘要

PurposeCetuximab in combination with chemotherapy is a standard-of-care first-line treatment regimen for patients with RAS wild-type (wt) metastatic colorectal cancer (mCRC); however, the efficacy of cetuximab plus leucovorin, fluorouracil, and oxaliplatin (FOLFOX) has never before been proven in a controlled and randomized phase III trial. To our knowledge, the TAILOR trial ( identifier: ) is the first randomized, multicenter, phase III study of the addition of cetuximab to first-line FOLFOX prospectively choosing a RAS wt population and thus providing confirmative data for the efficacy and safety of cetuximab plus FOLFOX versus FOLFOX alone.
机译:目的西妥昔单抗联合化疗是针对RAS野生型(wt)转移性结直肠癌(mCRC)患者的标准一线治疗方案;但是,西妥昔单抗联合亚叶酸钙,氟尿嘧啶和奥沙利铂(FOLFOX)的功效从未在对照和随机的III期临床试验中得到证实。据我们所知,TAILOR试验(标识符:)是将西妥昔单抗添加至一线FOLFOX中的第一项随机,多中心,III期研究,前瞻性选择了RAS wt人群,从而为西妥昔单抗plus的有效性和安全性提供了验证性数据。 FOLFOX与单独的FOLFOX。

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