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临床试验/NCT02595840
NCT02595840终止2 期

Biomarker Study Accompanying the AIO-TRK-0114 Study (MARBLE)

Universität Duisburg-Essen0 个研究点目标入组 4 人开始时间: 2015年11月25日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
4
主要终点
Progression-free Survival in relation to exploratory biomarkers

研究概览

简要总结

To compare the efficacy of afatinib maintenance with pemetrexed maintenance following induction therapy with platinum/ pemetrexed in patients with metastatic EGFR mutated non-small-cell lung cancer progressing after first-line treatment with afatinib as first tyrosine kinase inhibitor with respect to progression-free survival

详细描述

Patients who have progressed after first-line treatment with afatinib as first tyrosine kinase inhibitor (TKI) will be screened while they are receiving second-line (induction) treatment consisting of cisplatin / carboplatin plus pemetrexed given in 21-day cycles. Patients who do not progress (i.e. complete or partial response, or stable disease - CR, PR or SD) after completion of at least three and not more than four chemotherapy cycles will be randomized (1:1 ratio) to receive maintenance therapy with either afatinib (40 mg/d or last tolerated dose during first-line treatment with afatinib as first TKI) or pemetrexed (500 mg/m2 or 375 mg/m2 if dose reduction was required every 21 days) until disease progression or treatment discontinuation because of patient decision or toxicity.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Participation in the AIO-TRK-0114 (MARBLE) study (EudraCT-No. 2014-001983-36)
  • Written informed consent

排除标准

  • Patients who do not meet the inclusion criterial of the AIO-TRK-0114 (MARBLE) study (EudraCT-No. 2014-001983-36)

研究组 & 干预措施

Arm A: Afatinib

Experimental

Afatinib 40 mg/d (30, or 20 mg/d in case of dose reduction during 1st line treatment)

干预措施: Afatinib (Drug)

Arm B: Pemetrexed

Experimental

Pemetrexed 500 mg/m2 (375 mg/m² in case of dose reduction during induction therapy) i.v. on d1 of each 21-day cycle

干预措施: Pemetrexed (Drug)

结局指标

主要结局

Progression-free Survival in relation to exploratory biomarkers

时间窗: until progression

次要结局

  • Objective response rate(Assessed every 6 weeks for 24 weeks, then every 9 weeks)
  • Overall Survival in relation to exploratory biomarkers(continuous assessment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Martin Schuler, Prof. Dr. med.

Director, Department of Medical Oncology

Universität Duisburg-Essen

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