Protein and RNA Expression Patterns in Predicting Response to Treatment in Patients With Lung Cancer

Sponsor
Vanderbilt-Ingram Cancer Center (Other)
Overall Status
Completed
CT.gov ID
NCT00897650
Collaborator
National Cancer Institute (NCI) (NIH)
204
1
139
1.5

Study Details

Study Description

Brief Summary

RATIONALE: Studying samples of tumor tissue and blood in the laboratory from patients with cancer may help doctors learn more about changes that occur in genetic material (DNA and RNA) and may also identify protein expression patterns related to cancer. It may also help doctors predict how patients will respond to treatment.

PURPOSE: This research study evaluates changes in DNA, RNA, and proteins with the goal of predicting response to treatment in patients with lung cancer.

Condition or Disease Intervention/Treatment Phase
  • Genetic: DNA/RNA sequencing and expression levels
  • Genetic: Protein expression analysis
  • Procedure: Lung tumor biopsy
  • Procedure: Blood sample

Detailed Description

OBJECTIVES:
  • To determine protein and/or RNA expression patterns capable of predicting tumor response to therapy in tumor tissue samples from patients with lung cancer or suspected of having lung cancer.

  • To characterize the genes and proteins found to be predictive of response in order to help elucidate the molecular biology underlying cancer chemosensitivity.

  • To evaluate DNA mutations found within the lung cancer sample which may be predictive of response or resistance to certain therapeutic agents.

OUTLINE: Patients undergo collection of tumor tissue by percutaneous fine needle aspiration, core biopsy, thoracentesis, or during any medically indicated procedure involving removal of lung cancer tissue. Tissue samples are analyzed by a variety of techniques, including DNA sequencing, RNA sequencing and expression levels, protein assessment [by immunohistochemistry, western blot, Matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-MS]). The goal of these studies is to identify of gene mutations, gene expression levels, and proteins predictive of treatment response. Blood samples are also collected to obtain normal DNA for analysis.

After completion of study, patients will be followed until their death.

Study Design

Study Type:
Observational
Actual Enrollment :
204 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Molecular Fingerprints in Lung Cancer: Predicting Tumor Response to Therapy
Study Start Date :
Dec 1, 2005
Actual Primary Completion Date :
Jul 1, 2016
Actual Study Completion Date :
Jul 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Lung cancer

Patients with a diagnosis of invasive lung cancer.

Genetic: DNA/RNA sequencing and expression levels
Lung tumor tissue will be collected.

Genetic: Protein expression analysis
Lung tumor tissue will be collected.
Other Names:
  • Matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI)
  • Immunohistochemistry
  • Western blot
  • RPPA
  • Procedure: Lung tumor biopsy
    Tissue will be collected by percutaneous fine needle aspiration, a percutaneous core biopsy, or during a medically indicated procedure during which lung tumor tissue will be removed

    Procedure: Blood sample
    Patients will be asked for a venous blood sample

    Outcome Measures

    Primary Outcome Measures

    1. DNA, RNA, and Protein expression patterns and mutational analysis [After lung tumor tissue and blood collection.]

      DNA, RNA, and Protein expression patterns and mutation status in lung tumor tissue that are capable of predicting tumor response to therapy

    Secondary Outcome Measures

    1. Characterization of genes and proteins predictive of response to therapy [After lung tumor tissue and blood collection]

      Identify genes and proteins predictive of response to therapy and that can be used to identify novel mechanisms underlying lung cancer behavior

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 120 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Inclusion criteria

    • Diagnosis of suspected lung cancer or lung cancer

    Exclusion criteria

    • Inability to undergo therapy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Vanderbilt-Ingram Cancer Center Nashville Tennessee United States 37232-6838

    Sponsors and Collaborators

    • Vanderbilt-Ingram Cancer Center
    • National Cancer Institute (NCI)

    Investigators

    • Study Chair: Christine Lovly, MD, PhD, Vanderbilt-Ingram Cancer Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Christine Lovly, MD, PhD, Assistant Professor of Medicine and Cancer Biology, Vanderbilt-Ingram Cancer Center
    ClinicalTrials.gov Identifier:
    NCT00897650
    Other Study ID Numbers:
    • VICC THO 0547
    • P30CA068485
    • VU-VICC-THO-0547
    • P50CA090949
    First Posted:
    May 12, 2009
    Last Update Posted:
    Jul 19, 2017
    Last Verified:
    Jul 1, 2017
    Keywords provided by Christine Lovly, MD, PhD, Assistant Professor of Medicine and Cancer Biology, Vanderbilt-Ingram Cancer Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 19, 2017