PRIMARY OBJECTIVES:
I. To determine the effect of escalating doses of metformin (metformin hydrochloride) given pre-operatively on pancreatic cancer cell proliferation and apoptosis.
SECONDARY OBJECTIVES:
I. To assess toxicity of escalating doses of metformin given pre-operatively in patients with resectable pancreatic carcinoma.
II. To measure the effect of metformin on the expression of phosphorylated acetyl-CoA carboxylase alpha (ACC), phosphorylated mechanistic target of rapamycin (serine/threonine kinase) (mTOR), and pancreatic cancer stem cells.
OUTLINE: Patients are randomized to 1 of 3 treatment groups.
GROUP I: Patients undergo observation.
GROUP II: Patients receive metformin hydrochloride orally (PO) twice daily (BID) for at least 7 days in the absence of disease progression or unacceptable toxicity.
GROUP III: Patients receive metformin hydrochloride as in Group II.
After completion of study treatment, patients are followed up 30 days.