跳至主要内容
临床试验/NCT02623257
NCT02623257已完成不适用

A Diagnostic Study to Determine the Prevalence of Epidermal Growth Factor Receptor Mutations Assessed With Circulating Tumor DNA Samples in Advanced Non-small Cell Lung Cancer

First People's Hospital of Hangzhou1 个研究点 分布在 1 个国家目标入组 1,055 人开始时间: 2016年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,055
试验地点
1
主要终点
Proportion of patients with EGFR mutation detected by amplification refractory mutation system (ARMS) assay

研究概览

简要总结

The study aims to explore the prevalence of EGFR mutations assessed with ctDNA samples in advanced NSCLC, who had received ≤ 1 prior systemic chemotherapy regimens.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

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

  • Histologically confirmed stage IIIB/IV NSCLC;
  • Patient had received ≤ 1 prior systemic chemotherapy regimens;
  • Provision of blood (plasma) sample for ctDNA testing;
  • Patient must be able to comply with the protocol;

排除标准

  • Prior received ≥2 systemic chemotherapy regimens;
  • As judged by the investigator, any evidence of severe or uncontrolled systemic disease (e.g. unstable or uncompensated respiratory, cardiac, hepatic or renal disease);
  • Histologically confirmed small cell lung cancer or other metastatic tumors;
  • Patient with no histologic or cytological diagnosis;

结局指标

主要结局

Proportion of patients with EGFR mutation detected by amplification refractory mutation system (ARMS) assay

时间窗: up to 2 years

The investigators will describe the proportion of EGFR mutation on ctDNA detected by ARMS assay in patients with non-small cell lung cancer (NSCLC)

次要结局

  • Distribution of EGFR mutation by ARMS assays among the different Clinical characteristics(up to 2 years)
  • Proportion of patients after first-line chemotherapy failure with EGFR mutation detected by amplification refractory mutation system (ARMS) assay(up to 2 years)
  • Proportion of treatment-naive patients with EGFR mutation detected by amplification refractory mutation system (ARMS) assay(up to 2 years)

研究者

发起方
First People's Hospital of Hangzhou
申办方类型
Other
责任方
Sponsor

研究点 (1)

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