Trials / Completed
CompletedNCT02418234
T790M Mutation on ctDNA in Patients With NSCLC After EGFR-TKI Failure
Frequency and Abundance of T790M Mutation on Circulating Tumor DNA in Patients With Non-small Cell Lung Cancer After Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors Treatment Failure: a Perspective Observational Study
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 314 (actual)
- Sponsor
- First People's Hospital of Hangzhou · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the frequency and abundance of T790M mutation among the different Clinical modes of EGFR-TKI failure.
Detailed description
An observational, non-interventional, multi-central study of comparison of the frequency and abundance of T790M mutation using both amplification refractory mutation system (ARMS) and digital droplet PCR (ddPCR) methods among the different Clinical modes of non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) failure
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | mutation detection | |
| OTHER | ARMS and ddPCR | |
| GENETIC | ctDNA analysis |
Timeline
- Start date
- 2015-03-01
- Primary completion
- 2016-04-01
- Completion
- 2017-11-01
- First posted
- 2015-04-16
- Last updated
- 2018-03-12
- Results posted
- 2016-08-08
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT02418234. Inclusion in this directory is not an endorsement.