Feasibility Study of Lung Cancer Screening Using Cell-Free DNA Liquid Biopsy at Home in High-Risk Current and Former Smokers
Summary
This clinical trial investigates how practical and doable (feasibility) cell-free deoxyribonucleic acid (DNA) liquid biopsy is in screening high-risk patients for lung cancer. Currently, a low dose computed tomography (CT) scan is used to screen for lung cancer, however, due to various factors, few high-risk patients are screened. Liquid biopsy utilizes technology that can detect small amounts of DNA shed by cancer cells and may be able to spot lung cancer at an earlier stage. If a positive result comes back from the liquid biopsy, a patient may be more willing to get a low dose CT (LDCT) scan, possibly confirming the biopsy's findings and thus leading to more early lung cancer detection.
Detailed description
PRIMARY OBJECTIVE: I. To determine the feasibility of lung cancer screening using liquid biopsy in a community setting. SECONDARY OBJECTIVES: I. To determine screening follow-through rates in those who agreed to undergo screening by preferred modality (liquid biopsy versus \[vs\] LDCT). II. To determine the rate of LDCT following liquid biopsy (in those who underwent liquid biopsy) after stratifying by test result (negative versus positive). III. To compare participant sociodemographic factors (age, sex, race/ethnicity, educational background) and survey scores across screening preference (liquid biopsy vs. LDCT). OUTLINE: Participants choose 1 of 2 cohorts. COHORT A: Participants undergo collection of blood sample (liquid biopsy), with option to undergo LDCT if liquid biopsy results are positive. COHORT B: Participants undergo low dose CT with optional liquid biopsy on the same day as LDCT. After completion of study, patients are followed up at 6 months.
Arms & interventions
- ProcedureLiquid Biopsy
Undergo liquid biopsy
- ProcedureLow Dose Computed Tomography of the Chest
Undergo low dose CT
- OtherSurvey Administration
Ancillary studies
Outcome measures
Primary
Screening preference
The proportion of participants who agree to undergo lung cancer screening using liquid biopsy versus LDCT, with a feasibility threshold of at least 30% preferring liquid biopsy.
Time frame: Upon completion of home liquid biopsy or LDCT, an average of 4 weeks.
Secondary
Participants who follow-through on screening 1
Time frame: 6 month follow-up timepoint.
Participants who follow-through on screening 2
Time frame: 6 month follow-up timepoint.
Participants who follow-through on screening 3
Time frame: 6 month follow-up timepoint.
Participants who follow-through on screening 4
Time frame: 6 month follow-up timepoint.
Participants who undergo low dose computed tomography of the chest (LDCT) after receiving liquid biopsy results
Time frame: Up to 6 months
Sociodemographic factors (age, sex, race/ethnicity, educational background)
Time frame: At baseline visit
Survey scores across screening preference 1
Time frame: At 6 month follow up
Survey scores across screening preference 2
Time frame: At 6 month follow up
Survey scores across screening preference 3
Time frame: At 6 month follow up
Survey scores across screening preference 4
Time frame: At 6 month follow up
Survey scores across screening preference 5
Time frame: At 6 month follow up
Eligibility criteria
Study locations (1)
City of Hope Medical Center
Duarte, California, 91010