Development of a Model to Predict Progression Free Survival After Treatment With Erlotinib in E3503
Development of a Model to Predict Progression Free Survival After Treatment With Erlotinib in E3503
RATIONALE: Studying samples of tissue from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict how patients respond to treatment with erlotinib.
PURPOSE: This laboratory study is developing a model to predict progression-free survival after erlotinib in patients with non-small cell lung cancer.
OBJECTIVES:
OUTLINE: Tissue samples are analyzed by whole genome mapping for single nucleotide polymorphism (SNP) rate and by signal detection rate and by quantitative immunohistochemistry for mesenchymal (vimentin/cytokeratin) and epithelial (E-cadherin) marker transitions. After biomarker identification and gene mapping are complete, a model to predict progression-free survival in these patients is developed.
PROJECTED ACCRUAL: A total of 137 samples will be accrued for this study.
DISEASE CHARACTERISTICS:
Diagnosis of non-small cell lung cancer, including any of the following subtypes:
Stage IIIB or IV or recurrent disease
Must have received treatment with erlotinib hydrochloride on clinical trial ECOG-E3503
PATIENT CHARACTERISTICS:
PRIOR CONCURRENT THERAPY: