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Analysis of the Incidence of Expression of Tumor Antigens in Pathologically Proven Stage I, II and III Non-Small Cell Lung Cancer(NSCLC) in Asiatic Patients

GlaxoSmithKline (GSK) logo

GlaxoSmithKline (GSK)

Status

Completed

Conditions

Pathologically Proven Stage I, II and III Non-Small Cell Lung Cancer (NSCLC)

Treatments

Other: Data acquisition and analysis

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

This study aims to investigate the expression of Melanoma-associated antigen 3 (MAGE-A3), Melanoma-associated antigen C2 (MAGE-C2), New York esophageal squamous cell carcinoma 1 (NY-ESO-1), L antigen family member 1 (LAGE-1), Wilms' tumor gene (WT1) and PRAME (PReferentially expressed Antigen of MElanoma) tumor antigens in a large number of pathologically proven stage I, II and III NSCLC samples of Asiatic patients.

Full description

This study will be based upon the analysis of samples and patient-related data already available at the various investigation sites. There will be no study treatment and no study-specific procedure carried out on the patients.

Clinical data collected will include patient demographics (age, gender), Tumor, Node, Metastasis (staging system) [TNM stage], histopathologic description and the patient smoker status. Strict anonymity of patient data will be maintained.

This retrospective study is based upon the analysis of archived formalin-fixed paraffin-embedded tissue samples and patient-related data already available at the investigational site.

Enrollment

377 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

For inclusion of a tissue sample, all of the following criteria must be met:

  • The patient had pathologically proven stage I, II or III NSCLC.
  • All the data required are available from patient's records.
  • Many patients may no longer be alive, or no longer be in contact with the investigation sites. Thus, patients will not be required to give their informed consent before inclusion in the study.

Exclusion criteria

  • Not applicable

Trial design

377 participants in 1 patient group

Cancer Group
Description:
Patients with pathologically proven stage I, II and III NSCLC.
Treatment:
Other: Data acquisition and analysis

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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