CASCADE-LUNG is a multisite, prospective, observational, blood specimen collection study in the elevated-risk lung cancer screening population. The primary objective is to demonstrate the performance characteristics, including sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of the DELFI Lung Cancer Screening Test (DLCST) for the detection of pathologically-confirmed lung cancer in a screening population using LDCT, pathology, and follow-up as the reference method.
DELFI identifies circulating fragments of DNA (cfDNA) and plasma biomarkers to detect cancer. Participants will be enrolled into the DELFI-L201 study after informed consent and eligibility is confirmed. The study purpose is to validate the performance of the DELFI-based test for the detection of lung cancer among individuals eligible for routine lung cancer screening. Participants will have blood collected and medical record review at baseline and will have medical record reviews at additional timepoints.
Study Type
OBSERVATIONAL
Enrollment
11,935
Subjects enrolled in DELFI-L201 will have blood specimens collected (\~30 mL) at enrollment or up to 30 days after enrollment.
Performance characteristics (sensitivity, specificity, PPV, NPV) of the DLCST.
Time frame: Approximately 24 months
Performance characteristics (sensitivity, specificity, PPV, NPV) of the DLCST.
Time frame: Up to approximately 36 months
Adverse events (AEs) associated with the blood specimen collection.
Time frame: Point in time blood collection (1 day) at enrollment
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