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临床试验/NCT03519958
NCT03519958撤回不适用

An Observational, Multi-centre Study on EGFR T790M Mutation Testing Practices and Outcomes Conducted Among Locally Advanced/Metastatic NSCLC Patients Who Progressed on Previous EGFR Tyrosine-kinase Inhibitor (TKI) Therapy in Hong Kong

AstraZeneca0 个研究点开始时间: 2018年9月30日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
AstraZeneca
主要终点
EGFR T790M mutation prevalance

研究概览

简要总结

To describe the T790M mutation status of patients with locally advanced/metastatic NSCLC who progressed on previous EGFR TKI treatment in a real-world setting.

详细描述

This is a multi-center, observational study of patients with locally advanced/metastatic NSCLC who progressed on previous EGFR TKI treatment. Eligible patients will be recruited from participating sites in Hong Kong over a 12 months enrolment period.

Plasma and urine samples will be collected from enrolled patients. Plasma circulating tumor DNA (ctDNA) and urine ctDNA will be analyzed by droplet digital PCR (ddPCR) for detection of T790M mutation and EGFR sensitizing mutations. Patients who are T790M plasma-negative, regardless of the urine testing results, will be recommended to undergo re-biopsy (defined as tissue sampling or cytology sampling), tissue/cytology T790M testing, and to provide a second plasma sample for a second plasma T790M test (tested by ddPCR).

Enrolled patients who subsequently receive osimertinib treatment will be followed up as per routine practice at the investigational site. Patient data will be collected for 12 months or until death or loss to follow-up, whichever occurs earlier, from the first prescription of osimertinib. All clinical decisions will be at the discretion of the treating physician.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

EGFR T790M mutation prevalance

时间窗: 3 years

Based on the plasma-tissue testing algorithm in NSCLC patients who progressed on previous EGFR TKI therapy

次要结局

  • Demographics(Baseline)
  • Disease Characteristics(3 years)
  • Proportion of Valid Tissue T790M Testing Result(3 years)
  • False Negative Proportation(3 years)
  • Number of particapants with complications assoicated with re-biopsy(3 years)
  • Clinical Outcomes in tissue/cytology-positive(3 years)
  • T790M Plasma Outcome(3 years)
  • Reasons for not performing re-biopsy(3 years)
  • Clinical Outcomes in urine-positive(3 years)
  • Clinical Outcomes in T790M plasma-positive subejects(3 years)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

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