This study will evaluate the diagnostic performance of liquid biopsy for identifying molecular abnormalities among patients managed by the Multidisciplinary Molecular Biology Meeting. The gold standard considered in this study is the solid biopsy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
238
36 mL will be taken for the study.
Centre Antoine Lacassagne
Nice, France
RECRUITINGSensitivity of liquid biopsy versus solid biopsy (gold standard)
The primary endpoind is the sensitivity of liquid biopsy versus solid biopsy as the gold standard for detecting genomic alterations evaluated in the studied gene panel. The panel will consist of 70 genes common to the PanoraMix panels (125 genes, FFPE) and Avida (104 genes, cpDNA).
Time frame: 1 month
Specificity of liquid biopsy versus solid biopsy (gold standard)
The specificity of liquid biopsy versus solid biopsy as the gold standard in the detection of genomic alterations evaluated in the studied gene panel.
Time frame: 1 month
Failure rate of molecular screening
The failure rate of molecular screening (defined as the inability to provide the genetic profile from the liquid biopsy due to technical failure).
Time frame: 1 month
Clinical factors predictive of the sensitivity of liquid biopsy.
Clinical factors predictive of the sensitivity of liquid biopsy.
Time frame: 1 month
Rate of unexploitable results
The rate of unexploitable results, defined as the rate of results that do not allow for classification for each technique of the results as True Positive, False Positive, False Negative, or True Negative.
Time frame: 1 month
Time required to obtain each analysis
The time required to obtain each analysis, defined as the time between the prescription of the test and the delivery of the result.
Time frame: 1 month
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