Lung Cancer Clinical Trial
Official title:
COX-2 Activity in Early and Advanced NSCLC and The Effect of Short-Term Administration of Specific COX-2 Inhibitors (Celecoxib)
RATIONALE: Studying samples of tissue, blood, and urine 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 clinical trial is studying celecoxib in treating patients with stage I, stage
II, or stage IIIA non-small cell lung cancer.
OBJECTIVES:
- To assess cyclo-oxygenase-2 (COX-2) activity in patients with early-stage non-small
cell lung cancer (NSCLC) and correlate the results with serum vascular endothelial
growth factor (VEGF) levels, tumor microvessel density score, tumor prostaglandin E2
(PGE_2) and matrix metalloproteinases (MMP) levels, and the major urinary metabolite of
PGE_2, PGE-M.
- To assess the effect of specific COX-2 inhibitors (celecoxib) on COX-2 expression
within the primary tumor, serum VEGF levels and tumor microvascular density, tumor
PGE_2 and MMP levels, and urinary PGE-M in a cohort of patients with early-stage NSCLC.
OUTLINE: Patients receive oral celecoxib 400 mg twice a day for 5 days in the absence of
disease progression or unaccepted toxicity. Patients with early-stage disease then undergo
surgery.
Biopsy, serum, and urine samples are obtained at baseline and after celecoxib treatment. The
biopsy specimen are examined for the expression of cyclo-oxygenase-2 (COX-2), PGE_2, and
selected MMPs by immunohistochemistry, western blotting, and northern blotting. Serum and
urine samples are analyzed for VEGF and PGE-M expression. COX-2 tumor expression is
correlated with serum VEGF levels; tumor MMP-2, MMP-9, and PGE_2 expression; urinary PGE-M
and microvessel density scores.
;
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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