The purpose of this study is to test the safety of high dose omeprazole and see what effects that it has on patients with exocrine pancreatic cancer.
During this study patients will receive treatment of omeprazole at the dose depending on group enrollment * Group A will receive omeprazole 80 mg, twice a day for 12-14 days unless unacceptable toxicity * Group B, will receive omeprazole 20 mg, once a day for 12-14 days Patients will receive treatment for 2\~3 weeks during the study, and 2 months of follow up. Total accrual is anticipated to take 2 years.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
60
Treatment will consist of Omeprazole 12-14 days prior to surgical therapy of pancreatectomy.
Stephenson Cancer Center
Oklahoma City, Oklahoma, United States
RECRUITINGProportion
Proportion of subjects receiving study treatment without adverse events that would significantly delay the surgery
Time frame: 2 years
Safety and Tolerability
Frequency and severity of treatment related adverse events per CTCAE v5
Time frame: 2 years
v-ATPase LC3-I and LC3-II expression
v-ATPase LC3-I and LC3-II expression on pancreatic tumor
Time frame: 2 years
pH
pH of tumor tissue
Time frame: 2 years
Correlation
Correlation of biomarker changes with potential cancer cell apoptosis
Time frame: 2 years
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