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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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00897234
Enrollment
84
Registered
2009-05-12
Start date
2008-12-31
Completion date
2010-10-31
Last updated
2014-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

recurrent non-small cell lung cancer, stage I non-small cell lung cancer, stage II non-small cell lung cancer, stage IIIA non-small cell lung cancer, stage IIIB non-small cell lung cancer, stage IV non-small cell lung cancer

Brief summary

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.

Detailed description

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.

Interventions

OTHERMass Spectrometry

Levels of Cathepsin D (CD) and fatty acid synthase (FAS) will be measured using isobaric tag labeling coupled with mass spectrometry. RNA concentration will be measured using spectrophometer and purity will be analyzed.

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Non-Small Cell Lung Cancer Patients * Documented diagnosis of non-small cell lung cancer, any stage and any time point in the course of treatment (i.e., at diagnosis, during any treatment, and during post treatment surveillance) * 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

Exclusion criteria

* 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. Written consent must be given for both subjects and controls.

Design outcomes

Primary

MeasureTime frameDescription
Levels of cathepsin DAt Routine Follow-UpMeasure plasma CD levels in patients with non-small cell lung cancer and non-smoker healthy controls using mass spectrometry.

Secondary

MeasureTime frameDescription
Levels of fatty acid synthase (FAS)At Routine Follow-UpMeasure FAS levels in patients with non-small cell lung cancer and non-smoker healthy controls using mass spectrometry.
Global microRNA expressionAt Routine Follow-UpMeasure global microRNA expression by microarray analysis using Illumina probes.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026