Clinical Trials Directory

Trials / Unknown

UnknownNCT03546452

A Prospective Study to Evaluate the Consistency of Next-Generation Sequencing(NGS)-Panels by Using Malignant Hydrothorax Form NSCLC

A Prospective Study to Evaluate the Results of Different NGS- Panels in Mutation Detection and Tumor Mutation Burden(TMB) Calculation by Using Malignant Hydrothorax From NSCLC

Status
Unknown
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
Shanghai Chest Hospital · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers

Summary

A prospective study to evaluate consistency of different NGS-panel. Cell free DNA is purified from each malignant hydrothorax from NSCLC .Different NGS-panels are applied to perform in vitro diagnosis to detect Single Nucleotide Variants(SNV) and to calculate TMB value in these DNA samples.Consistency of enrolled NGS-panels are then evaluated by statistical analysis.

Detailed description

1. Chest Hospital in accordance with the clinical requirements of the treatment required to extract ML hydrothorax sent to hospital pathology department for exfoliated Cell diagnosis and production of cell wax block, while the additional responsibility for the extraction of hydrothorax 500ml, and collect 10ml venous blood sample, Venous blood samples are stored in either the A cell-free DNA Blood collection Tube (STRECK tube) or the ethylenediaminetetraacetic acid(EDTA) anticoagulant tube. 2. Amoy Diagnostics Co., Ltd. (AmoyDx) is responsible for plasma separation after sampling 2 hours, plasma is frozen by the chest Hospital, AmoyDx completes the purification of peripheral blood cells genomic DNA , and which is divided into 6 parts ,5 of which are send to in vitro diagnostic products (IVD) enterprises to perform NGS-Panel detection. 3. 100ml hydrothorax is send to each IVD enterprise. 4. Each IVD enterprise carries on the hydrothorax cell free DNA and peripheral blood cell genomic DNA NGS-Panel detection according to their own protocol. 5. Each IVD enterprise will complete the test within 7-10 working days and fill out the results in accordance with the report template provided by this research project (provided by Guangzhou Burning Rock Medical Examination Institute Co., Ltd.) and submit to sponsor by email. 6. Sponsor would use whole exon panel (WES) to obtain an TMB value if needed. 7. Employ four-grid analysis to evaluate positive compliance rate, negative compliance rate, total compliance rate of all submitted data. 8. Employ kappa test to evaluate the consistency of each two detections.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTin vitro NGS-panelcell free DNA ,which was purified from hydrothorax, is used to be tested by NGS-panel

Timeline

Start date
2018-05-18
Primary completion
2018-09-30
Completion
2019-05-01
First posted
2018-06-06
Last updated
2018-06-07

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03546452. Inclusion in this directory is not an endorsement.