Biomarker Study Accompanying the AIO-TRK-0114 Study (MARBLE)
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
- 否
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
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
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
Martin Schuler, Prof. Dr. med.
Director, Department of Medical Oncology
Universität Duisburg-Essen
