Vitamin E δ-Tocotrienol Administered to Subjects With Resectable Pancreatic Exocrine Neoplasia

Inclusion Criteria: * The patient has a resectable tumor or cyst arising from the pancreatic exocrine gland (pancreatic ductal adenocarcinoma, intraductal papillary mucinous neoplasm of the pancreas, or mucinous cystic neoplasm of the pancreas) and is undergoing surgical resection of the neoplasm. * The patient is not a candidate for neoadjuvant chemoradiation therapy (i.e., patients with borderline resectable pancreatic ductal adenocarcinoma who are known to benefit from neoadjuvant treatment regimens). * The patient has an Eastern Cooperative Oncology Group (ECOG) performance status of ≤2. * The patient has adequate organ function as follows: Serum creatinine ≤1.5 mg/dL or calculated creatinine clearance \>60 mL/min; Bilirubin ≤ the institutional upper limit of normal (ULN); Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 times the upper limit of normal if no liver involvement or ≤5 times the upper limit of normal with liver involvement; absolute neutrophil count (ANC) ≥ 1000mm³; Platelet count ≥100,000/mm³. * The patient has the capability of understanding the informed consent document and has signed the informed consent document. * Sexually active patients (male and female) must use medically acceptable methods of contraception during the course of the study. * Female patients of childbearing potential must have a negative pregnancy test at screening. * Able to understand and comply with the requirements of the protocol. Exclusion Criteria: * T…