Purpose

This research trial studies the long term follow-up for early detection of lung cancer in current or former smokers. Following up on smokers by collecting and analyzing specimens in the laboratory, performing chest computed tomography (CT) scans, as well as reviewing medical records may help doctors detect lung cancer at an earlier stage.

Condition

Eligibility

Eligible Ages
Between 55 Years and 80 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Current smoker or former smoker, if former smoker participants must have quit smoking within the past 15 years - >= 30 pack year of smoking history - Participant is uninsured

Exclusion Criteria

  • History of diagnosis/treatment of lung cancer in the past 2 years - History of head/neck or esophageal cancer in the last 1 year - Inability to provide informed consent

Study Design

Phase
Study Type
Observational
Observational Model
Case-Only
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Screening Patients are followed up at 1, 2, 3, 4, and 5 years and undergo collection of sputum, nasal epithelium, buccal epithelium, blood, and urine samples. Patients also undergo pulmonary function tests, chest CT, and review of medical records
  • Procedure: Biospecimen Collection
    Undergo collection of sputum
  • Procedure: Biospecimen collection
    Undergo collection of nasal epithelium
  • Procedure: Biospecimen collection
    Undergo collection of buccal epithelium
  • Procedure: Biospecimen collection
    Undergo collection of blood
  • Procedure: Biospecimen collection
    Undergo collection of urine
  • Procedure: Pulmonary Function Test
    Undergo pulmonary function test
  • Procedure: Computed Tomography (CT)
    Undergo chest CT
    Other names:
    • Undergo chest CT
  • Other: Laboratory Biomarker
    Correlative studies

More Details

Status
Active, not recruiting
Sponsor
Vanderbilt-Ingram Cancer Center

Study Contact

Detailed Description

PRIMARY OBJECTIVES: I. To provide screening for lung cancer in an underserved and high risk population for lung cancer. II. To collect clinical and demographic information and research bio specimens prospectively on high risk individuals. III. To analyze the association between suspected lung cancer risk factors and outcomes such as pre-malignant lesions and diagnosis of lung cancer. IV. To identify and validate biomarkers that are associated with lung cancer risk factors and premalignant lesions. V. To assess the association between patient characteristics and test results to the genetic and histological characteristics of lung preinvasive lesions and cancers. VI. To describe this high-risk cohort and to identify the patients eligible for future clinical trials (e.g. chemoprevention). OUTLINE: Patients are followed up at 1, 2, 3, 4, and 5 years and undergo collection of sputum, nasal epithelium, buccal epithelium, blood, and urine samples. Patients also undergo pulmonary function tests, chest CT, and review of medical records.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.