...
首页> 外文期刊>Clinical lung cancer >Rationale and Study Design of the IRENE-Trial (NVALT-16): A Phase II Trial to Evaluate Iressa Rechallenge in Advanced NSCLC Patients With an Activating EGFR Mutation Who Responded to an EGFR-TKI Used As First-Line or Previous Treatment
【24h】

Rationale and Study Design of the IRENE-Trial (NVALT-16): A Phase II Trial to Evaluate Iressa Rechallenge in Advanced NSCLC Patients With an Activating EGFR Mutation Who Responded to an EGFR-TKI Used As First-Line or Previous Treatment

机译:IRENE试验(NVALT-16)的原理和研究设计:评估具有激活EGFR突变且对EGFR-TKI用作一线或先前治疗有反应的晚期NSCLC患者的易瑞沙再挑战的II期试验

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Background: Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) have shown improved progression-free survival (PFS) and overall survival (OS) over chemotherapy in a molecularly defined subgroup of advanced non-small-cell lung cancer (NSCLC) patients (ie, patients with an activating mutation in the EGFR gene). Nevertheless, all EGFR-mutated NSCLC patients develop TKI resistance eventually and there is no registered treatment or therapeutic strategy available for these patients. Several retrospective or small cohort studies have described patients who re-responded to EGFR-TKI treatment after a TKI-free interval ('drug holiday'). To date, no large prospective evaluation of the clinical effects of EGFR-TKI rechallenge in EGFR-mutated NSCLC patients has been performed. Patients and Methods: The IRENE (Iressa RE-challenge in advanced, EGFR-mutated NSCLC patients who responded to an EGFR-TKI used as first-line or previous treatment) (Dutch association for pulmonologists [NVALT]-16) trial is a multicenter, open-label, single-arm, single-stage, phase II study to evaluate gefitinib rechallenge in EGFR-mutated NSCLC patients who were previously treated with a TKI followed by a subsequent line of treatment (excluding EGFR-TKIs). The primary objective is disease control rate according to Response Evaluation Criteria in Solid Tumors criteria. Secondary objectives are objective response rate, PFS, OS, mutation characterization of sequential biopsies, VeriStrat correlation to PFS and OS, analysis of tumor-derived RNA in blood platelets and analysis of cell-free DNA in blood plasma. Results: The IRENE (NVALT-16) trial will evaluate the safety, efficacy, and feasibility of readministration of gefitinib after an EGFR-TKI-free interval in EGFR-mutated NSCLC patients. Conclusion: The study will evaluate gefitinib re-challenge in EGFR-mutated NSCLC patients. The study will also provide more insight into the dynamic development of molecular characteristics of EGFR-mutated NSCLC along the course of the disease. (C) 2015 Elsevier Inc. All rights reserved.
机译:背景:表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKIs)已显示在晚期非小细胞肺癌(NSCLC)的分子定义亚组中,化学疗法的无进展生存期(PFS)和总体生存期(OS)均得到了改善患者(即具有EGFR基因激活突变的患者)。尽管如此,所有EGFR突变的NSCLC患者最终都会发展为TKI耐药性,并且没有针对这些患者的注册治疗或治疗策略。几项回顾性研究或小型队列研究已经描述了在无TKI间隔后(“药物假期”)对EGFR-TKI治疗产生反应的患者。迄今为止,尚未对EGFR突变的NSCLC患者中EGFR-TKI再挑战的临床效果进行大的前瞻性评估。患者和方法:IRENE(对EGFR-TKI作为一线或先前治疗有反应的晚期,EGFR突变的晚期NSCLC患者的Iressa RE挑战)(荷兰肺病学家协会[NVALT] -16)试验是一个多中心试验,开放标签,单臂,单阶段,II期研究,评估吉非替尼在先前经TKI继之以后续治疗(不包括EGFR-TKIs)治疗的EGFR突变NSCLC患者中的再挑战。主要目标是根据实体肿瘤反应评估标准中的疾病控制率。次要目标是客观应答率,PFS,OS,连续活检的突变特征,与PFS和OS的VeriStrat相关性,对血小板中肿瘤来源的RNA的分析以及血浆中无细胞DNA的分析。结果:IRENE(NVALT-16)试验将评估在EGFR突变的NSCLC患者中,无EGFR-TKI间隔后吉非替尼重新给药的安全性,疗效和可行性。结论:这项研究将评估吉非替尼对EGFR突变的NSCLC患者的再挑战。该研究还将提供更多关于EGFR突变的NSCLC在疾病过程中分子特征动态发展的见解。 (C)2015 Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号