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首页> 外文期刊>Clinical lung cancer >Rationale for treatment and study design of tailor: a randomized phase III trial of second-line erlotinib versus docetaxel in the treatment of patients affected by advanced non-small-cell lung cancer with the absence of epidermal growth factor receptor mutations.
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Rationale for treatment and study design of tailor: a randomized phase III trial of second-line erlotinib versus docetaxel in the treatment of patients affected by advanced non-small-cell lung cancer with the absence of epidermal growth factor receptor mutations.

机译:治疗的理由和量身定制的研究设计:厄洛替尼与多西紫杉醇二线治疗不存在表皮生长因子受体突变的晚期非小细胞肺癌患者的三线随机试验。

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摘要

We present the rationale and study design of the Tarceva Italian Lung Optimization trial phase III, multicenter, open-label, randomized trial on efficacy of second-line therapies in different subgroups of non-small-cell lung cancer (NSCLC) patients identified using molecular and clinical evaluations. To date, we can assume that advanced NSCLC epidermal growth factor receptor (EGFR)-mutated patients benefit from EGFR tyrosine kinase inhibitors, such as gefitinib and erlotinib, whereas their role in the treatment of patients who do not have EGFR mutations is controversial. The aim of this study is to assess whether it is possible to optimize second-line treatment in NSCLC patients with absence of EGFR mutations. Moreover, the predictive value of the K-ras mutation, EGFR protein expression, and EGFR gene copy number, as well as a smoking habit and histotype for determining a different effect of erlotinib compared with chemotherapy will be assessed in patients who do not have EGFR mutations. The primary endpoint is overall survival; the secondary endpoints are progression-free survival, response rate, quality of life, and toxicity. We have planned to collect blood samples to identify different prognosis-related polymorphisms and to assess their sensitivity and specificity in the detection of EGFR and K-ras mutations with respect to histologic samples.
机译:我们提供了Tarceva Italian Lung Optimization试验第三阶段(多中心,开放标签,随机试验)的理论依据和研究设计,该试验针对使用分子鉴定的非小细胞肺癌(NSCLC)不同亚组的二线疗法的疗效和临床评估。迄今为止,我们可以假定晚期NSCLC表皮生长因子受体(EGFR)突变的患者受益于EGFR酪氨酸激酶抑制剂,如吉非替尼和厄洛替尼,而它们在治疗无EGFR突变的患者中的作用尚存争议。这项研究的目的是评估在没有EGFR突变的NSCLC患者中是否有可能优化二线治疗。此外,在没有EGFR的患者中,将评估K-ras突变,EGFR蛋白表达和EGFR基因拷贝数的预测价值,以及吸烟习惯和组织类型对确定厄洛替尼与化疗相比具有不同作用的预测价值。突变。主要终点是总体生存率;次要终点是无进展生存期,缓解率,生活质量和毒性。我们计划收集血液样本以鉴定不同的预后相关多态性,并评估它们在检测与组织学样本有关的EGFR和K-ras突变中的敏感性和特异性。

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