首页> 外文期刊>Journal of Clinical Oncology >LUX-Lung 4: A Phase II Trial of Afatinib in Patients With Advanced Non-Small-Cell Lung Cancer Who Progressed During Prior Treatment With Erlotinib, Gefitinib, or Both.
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LUX-Lung 4: A Phase II Trial of Afatinib in Patients With Advanced Non-Small-Cell Lung Cancer Who Progressed During Prior Treatment With Erlotinib, Gefitinib, or Both.

机译:LUX-Lung 4:Afatinib在晚期非小细胞肺癌患者中进行的II期临床试验,这些患者在先前用厄洛替尼,吉非替尼或两者同时治疗期间进展。

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New molecular targeted agents are needed for patients with non-small-cell lung cancer (NSCLC) who progress while receiving erlotinib, gefitinib, or both. Afatinib, an oral irreversible ErbB family blocker, has preclinical activity in epidermal growth factor receptor (EGFR [ErbB1]) mutant models with EGFR-activating mutations, including T790M.This was a Japanese single-arm phase II trial conducted in patients with stage IIIB to IV pulmonary adenocarcinoma who progressed after ≥ 12 weeks of prior erlotinib and/or gefitinib. Patients received afatinib 50 mg per day. The primary end point was objective response rate (complete response or partial response) by independent review. Secondary end points included progression-free survival (PFS), overall survival (OS),
机译:非小细胞肺癌(NSCLC)的患者在接受厄洛替尼,吉非替尼或同时接受治疗和治疗的同时进展,需要新的分子靶向药物。口服不可逆性ErbB家族阻滞剂Afatinib在具有EGFR激活突变的表皮生长因子受体(EGFR [ErbB1])突变体模型(包括T790M)中具有临床前活性。这是一项针对IIIB期患者的日本单臂II期临床试验在先前的厄洛替尼和/或吉非替尼≥12周后发展为IV型肺腺癌。患者每天接受阿法替尼50 mg治疗。主要终点是通过独立评审的客观缓解率(完全缓解或部分缓解)。次要终点包括无进展生存期(PFS),总体生存期(OS),

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