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Detection of Early Lung Cancer by Serum Protein Expression Profiling

University of British Columbia logo

University of British Columbia

Status

Unknown

Conditions

Non-small Cell Lung Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT00175578
C04-0640

Details and patient eligibility

About

Promising new technology exists to examine small proteins that are shed by cancers into the blood stream. The purpose of this study is to see if there are differences in the proteins and protein levels in blood from individuals with early stage lung cancer compared to healthy adults.

Full description

A prospective longitudinal patient-based pilot study is proposed whereby surfaced enhanced laser desorption ionization time-of-flight mass spectroscopy (SELDI-TOF-MS) will be used to discover and validate serum proteomic expression profiles diagnostic of early lung cancer. A unique approach will be used to compare the serum proteomic expression profiles of patients with non-small cell lung cancer compared to healthy heavy smoking adults, as well as differences before and after anatomic pulmonary resection with curative intent. Discriminatory proteins will be selected by their differential expression before compared to after surgical removal of a tumor. The protein profile of blood obtained from the draining pulmonary vein at the time of resection will be used to identify materials potentially shed by the tumor that may serve as biomarkers in peripheral blood. The serum samples will be used to develop a training data set and then a test set for validation using a class prediction model. Candidate proteomic patterns will then serve as a basis for a larger prospective multi-centre clinical trial.

Enrollment

220 estimated patients

Sex

All

Ages

45 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Presence of early stage non-small cell lung cancer
  • Elective surgical resection of lung lesion at Vancouver General Hospital (VGH)
  • No preoperative chemoradiation therapy
  • No previous cancer
  • Ability to provide informed consent

Trial contacts and locations

1

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Central trial contact

Jennifer Rattenbury

Data sourced from clinicaltrials.gov

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