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Clinical Trials/NCT00899457
NCT00899457
Completed
Not Applicable

Molecular Predictors of Lung Cancer Behavior: Controls

Vanderbilt-Ingram Cancer Center3 sites in 1 country37 target enrollmentApril 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy, no Evidence of Disease
Sponsor
Vanderbilt-Ingram Cancer Center
Enrollment
37
Locations
3
Primary Endpoint
Collection of biological specimens to use as controls in the study of lung cancer progression
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

RATIONALE: Studying samples of blood, urine, sputum, mouth cells, and bronchial tissue from healthy participants in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors learn more about the development of cancer.

PURPOSE: This laboratory study is looking for molecular markers in predicting lung cancer development using tissue samples from healthy participants.

Detailed Description

OBJECTIVES: * To obtain biological specimens from healthy participants with no known risk of lung cancer to use as controls in the study of lung cancer progression. * To identify new molecular abnormalities specific to the development of squamous cell carcinoma of the lung. OUTLINE: Serum, urine, sputum, and buccal cell samples are collected. Patients also undergo bronchoscopy for collection of bronchial tissue and bronchial brush samples. The samples are used for genomic and proteomic studies to identify new molecular abnormalities specific to the development of lung cancer.

Registry
clinicaltrials.gov
Start Date
April 2008
End Date
August 2010
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pierre P. Massion, MD

Associate Professor of Medicine (Allergy, Pulmonary & Critical Care) and Cancer Biology; Pulmonary and Critical Care Medicine Doctor

Vanderbilt-Ingram Cancer Center

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Collection of biological specimens to use as controls in the study of lung cancer progression

Time Frame: Off study date, up to one year

Specimens are collected from healthy participants with no known risk of lung cancer

Secondary Outcomes

  • Selection of important genes/proteins differentially expressed between study groups (e.g., normal vs low-grade vs high-grade vs invasive) and between normal smokers vs normal non-smokers(off-study date, up to one year)
  • Identification of new molecular abnormalities specific to the development of squamous cell carcinoma of the lung(off-study date, up to one year)

Study Sites (3)

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