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Blood Samples From Patients With Non-Small Cell Lung Cancer and From Healthy Volunteers
This study is currently recruiting participants.
Study NCT00897234   Information provided by National Cancer Institute (NCI)
First Received: May 9, 2009   Last Updated: June 16, 2009   History of Changes

May 9, 2009
June 16, 2009
December 2008
April 2010   (final data collection date for primary outcome measure)
Levels of cathepsin D [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00897234 on ClinicalTrials.gov Archive Site
Levels of fatty acid synthase [ Designated as safety issue: No ]
Same as current
 
Blood Samples From Patients With Non-Small Cell Lung Cancer and From Healthy Volunteers
Plasma Quantification of Cathepsin D and FAS in Non-Small Cell Lung Cancer

RATIONALE: Studying samples of blood from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer.

PURPOSE: This research study is looking at blood samples from patients with non-small cell lung cancer and from healthy volunteers.

OBJECTIVES:

  • Measure plasma cathepsin D levels in patients with non-small cell lung cancer and in healthy volunteers using mass spectometry.
  • Measure fatty acid synthase levels in these patients and healthy volunteers using mass spectometry.

OUTLINE: Blood samples are collected from patients and healthy volunteers to measure the levels of cathepsin D and fatty acid synthase by proteomic profiling and mass spectrometry.

 
Observational
 
Lung Cancer
  • Genetic: proteomic profiling
  • Other: laboratory biomarker analysis
  • Other: mass spectrometry
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
100
 
April 2010   (final data collection date for primary outcome measure)

DISEASE CHARACTERISTICS:

  • Must meet one of the following criteria:

    • Documented diagnosis of non-small cell lung cancer

      • Any stage
      • Any time point in the course of treatment
      • Measurable disease by CT scan within the past 4 weeks
    • Healthy volunteer

      • Non-smoking, defined as < 5 packs/year history of smoking and cessation of smoking ≥ 6 months ago OR a never smoker
      • Not regularly exposed (i.e., daily) to second-hand smoke

PATIENT CHARACTERISTICS:

  • No severe underlying lung disease (i.e., chronic obstructive pulmonary disease with FEV_1 < 1.0 L, pulmonary fibrosis, bronchiectasis, cystic fibrosis, etc.) as determined by enrolling researcher

PRIOR CONCURRENT THERAPY:

  • Not specified
Both
18 Years and older
Yes
 
United States
 
NCT00897234
Robert Arthur Kratzke, Masonic Cancer Center at University of Minnesota
CDR0000631983, UMN-2008NTLS094, 08O9M47482
Masonic Cancer Center, University of Minnesota
National Cancer Institute (NCI)
Principal Investigator: Robert A. Kratzke, MD Masonic Cancer Center, University of Minnesota
National Cancer Institute (NCI)
June 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP