Biomarkers for Diagnosis of Lung Nodules

Sponsor
University of Colorado, Denver (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT01085864
Collaborator
(none)
468
1
212.7
2.2

Study Details

Study Description

Brief Summary

A need exists for non-invasive testing to aid in clinical decision-making for Computerized Tomography (CT) scan detected lung nodules of indeterminate etiology. The investigators hypothesize that biomarkers detectable in blood, sputum or urine may be useful for guiding clinical decisions in the setting of CT detected lung nodules to determine which nodules are malignant and which are benign. The investigators also hypothesize that these biomarkers will decrease in concentration to the normal range after successful surgical treatment of malignant lung nodules.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The Biomarkers for Diagnosis of Lung Nodules Study is a prospective study of a cohort of 500 individuals with lung nodules of indeterminate etiology that are identified by CT scans. Either biopsy or repeat CT scans must be clinically indicated to determine the etiology of the nodule. Patients will be asked to allow investigators access to CT scan images and spirometry data, and provide blood, sputum, urine, and exhaled breath samples over the course of the study. Patients will also be asked to allow investigators to access pathology records if a biopsy or surgical excision of the nodule is clinically indicated.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    468 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Biomarkers for Diagnosis of Lung Nodules
    Actual Study Start Date :
    Jan 8, 2010
    Anticipated Primary Completion Date :
    Nov 1, 2026
    Anticipated Study Completion Date :
    Oct 1, 2027

    Arms and Interventions

    Arm Intervention/Treatment
    Patients with lung nodules on CT scan.

    Patients with lung nodules on CT scan.

    Outcome Measures

    Primary Outcome Measures

    1. Evaluation of biomarkers in blood, sputum or urine. [Baseline, 3-6 months, 12 months, 24 months, time of biopsy or surgery (if applicable), and 6 months post surgery (if applicable).]

      The primary hypothesis is that biomarkers detectable in blood, sputum, or urine will be useful for guiding clinical decisions in the setting of CT detected lung nodules.

    Secondary Outcome Measures

    1. Evaluation of biomarkers after successful surgical treatment of malignant lung nodules. [Within 3 years]

      The secondary hypothesis is that these biomarkers will decrease in concentration to the normal range after successful surgical treatment of malignant lung nodules.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 85 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Adult 18-85 years of age

    2. Patients referred to pulmonologists, oncologists, or thoracic surgeons for the evaluation of peripheral lung nodules found on CT scan.

    3. Repeat CT scans, biopsy or surgical excision are clinically indicated to determine the etiology of the nodule.

    4. One or more lung nodules must be between 8 mm and 30 mm in the greatest diameter.

    5. Patients must be fully informed of the investigational nature of the procedure and sign an informed consent.

    Exclusion Criteria:
    1. Lung nodules or masses greater than 30 mm in the greatest dimension.

    2. Lung nodules that have solid calcification.

    3. Lung nodules or masses with CT evidence of partial or complete obstruction of a lobar bronchus, main stem bronchus or the trachea.

    4. No prior cancer with the exception of non-melanoma skin cancer.

    5. Life expectancy of < 6 months

    6. Any individual who does not give oral and written consent for participation -

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Colorado Anschutz Medical Campus Aurora Colorado United States 80045

    Sponsors and Collaborators

    • University of Colorado, Denver

    Investigators

    • Principal Investigator: York E Miller, M.D., University of Colorado, Denver

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Colorado, Denver
    ClinicalTrials.gov Identifier:
    NCT01085864
    Other Study ID Numbers:
    • 09-1106.cc
    First Posted:
    Mar 12, 2010
    Last Update Posted:
    Nov 4, 2021
    Last Verified:
    Nov 1, 2021

    Study Results

    No Results Posted as of Nov 4, 2021