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临床试验/NCT03381066
NCT03381066Unknown3 期

A Phase III, Randomized, Multi-center Study to Determine the Efficacy of the Intercalating Combination Treatment of Chemotherapy and Gefitinib or Chemotherapy as Adjuvant Treatment in NSCLC With Common EGFR Mutations.

Yonsei University1 个研究点 分布在 1 个国家目标入组 225 人开始时间: 2018年4月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
入组人数
225
试验地点
1
主要终点
disease-free survival

研究概览

简要总结

This study aims to compare the efficacy of intercalating chemotherapy (gefitinib and pemetrexed/cisplatin) and chemotherapy (navelbine/cisplatin) in completely resected NSCLC with common EGFR mutations.

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
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Completely resected non-squamous cell NSCLC with stage IIa to IIIb (excluding N3) according to Version 8 of the IASLC Staging Manual in Thoracic Oncology
  • Tumors with common EGFR mutations (19del or L858R)
  • Adequate oran function

排除标准

  • Patients who were exposed to the chemotherapy or EGFR TKIs for NSCLC.
  • Patients with interstitial lung disease

研究组 & 干预措施

Intercalating arm

Experimental

gefitinib, pemetrexed,cisplatin

干预措施: gefitinib, pemetrexed,cisplatin (Drug)

chemotherapy alone arm

Active Comparator

Vinorelbine, cisplatin

干预措施: Vinorelbine, cisplatin (Drug)

结局指标

主要结局

disease-free survival

时间窗: 5 years

Time from the randomization to recurrence or any cause of death.

次要结局

  • Overall survival(5 year)
  • Number of participants with treatment-related adverse events as assessed by CTCAE4.0(5 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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