Combination Chemotherapy Before and After Surgery in Treating Patients With Localized Pancreatic Cancer

You may be eligible if

• Pathologic or cytologic documentation of pancreatic adenocarcinoma
• Resectable pancreatic adenocarcinoma disease as defined as follows:
• * No evidence of extrapancreatic disease by cross sectional imaging, PET scan, or laparoscopy, including nodal involvement beyond the peripancreatic tissues and/or distant metastases;
• * No evidence of tumor extension to superior mesenteric artery, hepatic artery, celiac axis, aorta, or inferior vena cava, and no evidence of occlusion or encasement of the superior mesenteric vein or superior mesenteric vein/portal vein confluence, as assessed by computed tomography (CT) using pancreatic protocol (or magnetic resonance imaging \[MRI\] in patients who cannot undergo CT) and EUS
• No prior treatment (chemotherapy, biological therapy, or radiotherapy) for resectable pancreatic cancer
• No prior treatment with oxaliplatin, irinotecan (irinotecan hydrochloride), fluorouracil or capecitabine
• Patients who received chemotherapy \> 5 years ago for malignancies other than pancreatic cancer are eligible
• There is no evidence of the second malignancy at the time of study entry
• \> 4 weeks since major surgery
• No other concurrent anticancer therapy
• Eastern Cooperative Oncology Group (ECOG) performance status: 0-1
• No other malignancy within past five years except basal cell carcinoma of the skin, cervical carcinoma in situ, or non-metastatic prostate cancer
• Paraffin block or slides must be available
• Adequate organ function
• No interstitial pneumonia or extensive and symptomatic interstitial fibrosis of the lung
• No \>= grade 2 sensory peripheral neuropathy
• No uncontrolled seizure disorder, active neurological disease, or known central nervous system (CNS) disease
• No significant cardiac disease, including the following: unstable angina, New York Heart Association class II-IV congestive heart failure, myocardial infarction within six months prior to study enrollment
• No history of chronic diarrhea
• Not pregnant and not nursing
• No other medical condition or reason that, in the opinion of the investigator, would preclude study participation
• Absolute neutrophil count \>= 1,500/uL
• Platelet count \>= 100,000/uL
• Hemoglobin \>= 9 g/dL
• Creatinine \< 1.5 X upper limit of normal (ULN) or
• Estimated glomerular filtration rate (GFR) \> 30 ml/min
• Bilirubin =\< 1.5 X ULN
• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =\< 3 X ULN
• Negative pregnancy test in women of childbearing age