This study aims to look at a comparison of liquid biopsy (blood sample) analysis compared with tissue biopsy in patients with advanced lung cancer
The primary aim of this study is to investigate the concordance of Inivata liquid biopsy panel with standard tissue biopsy analysis for detecting genomic alterations in patients with advanced non-squamous non-small cell lung cancer (NSCLC).
Study Type
OBSERVATIONAL
Enrollment
34
Mercy Hospital Cancer Center/Clinical Research
Fort Smith, Arkansas, United States
Mercy Cancer Center
Joplin, Missouri, United States
Mercy Clinic
Springfield, Missouri, United States
Mercy Clinic Oncology & Hematology
Oklahoma City, Oklahoma, United States
Concordance in the detection of molecular abnormalities using Inivata liquid biopsy panel with detection using standard of care tissue biopsy analysis.
The primary endpoint is concordance in detecting molecular abnormalities using Inivata liquid biopsy panel compared with detection using tissue biopsy analysis.
Time frame: 12 months
Sensitivity of Inivata liquid biopsy analysis relative to matched tissue analysis
Detection of sensitivity of molecular abnormalities using Inivata liquid biopsy panel relative to standard of care tissue biopsy analysis
Time frame: 12 months
Specificity of Inivata liquid biopsy analysis relative to matched tissue analysis
Detection of specificity of molecular abnormalities using Inivata liquid biopsy panel relative to standard of care tissue biopsy analysis
Time frame: 12 months
Description of the ctDNA profile of genomic alterations in patients where tumour tissue is limited versus that observed where tumour biopsy is achieved
Description of the ctDNA profile of genomic alterations in patients where tumour tissue is limited (Quantity Not Sufficient) versus that observed where tumour biopsy is achieved.
Time frame: 12 months
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Lehigh Valley Health Networks
Allentown, Pennsylvania, United States
Gibbs Cancer Center & Research Institute
Spartanburg, South Carolina, United States