Metformin Hydrochloride in Preventing Esophageal Cancer in Patients With Barrett Esophagus

Inclusion Criteria:

Histologically confirmed diagnosis of Barrett esophagus, with no dysplasia, indeterminate for dysplasia, or low-grade dysplasia as defined by the presence of specialized columnar epithelium on histology and >= 2 cm of involvement on endoscopy
Adequate Barrett mucosa, which is defined as >= 1 out of 4 research samples (i.e., >= 25%) with >= 50% intestinal metaplasia in biopsies required to satisfy the endpoints of the study
No history of esophageal carcinoma or other cancer(s) (except for non-melanoma skin cancers)
No erosive esophagitis or ulcerative esophagitis, unless treatment with a proton pump inhibitor (PPI) results in healed erosions or ulcers prior to entry endoscopy

No history of high-grade dysplasia or cancer (confirmed locally by esophagogastroduodenoscopy [EGD] and Pathology reports)

No ulcer, plaque, nodule, stricture, or other luminal irregularity within the Barrett segment, unless clinical biopsy produces no evidence of high-grade dysplasia or cancer
ECOG performance status =< 1
Hemoglobin >= 10 g/dL
Leukocytes >= 3,000/mL (>= 2,500/mL for African-American participants)
Absolute neutrophil count >= 1,500/mL (>= 1,000/mL for African-American participants)
Platelets >= 100,000/mL
Total bilirubin =< institutional upper limit of normal (ULN)
AST (SGOT) and ALT (SGPT) =< 1.5 times institutional ULN
Creatinine =< institutional ULN
Willingness to provide tissue samples for research purposes
No contraindication to esophagogastroduodenoscopy (EGD)
Willingness, for both men and women, to use adequate contraception (hormonal or barrier method of birth control; surgical intervention; abstinence) prior to study entry and for the duration of study participation
A negative (serum or urine) pregnancy test done =< 7 days prior to Pre-Registration, for women of childbearing potential only
No pregnant or nursing women
No participants with diabetes mellitus
No history of vitamin B12 deficiency or megaloblastic anemia
No history of lactic acidosis
No diseases associated with weight loss: anorexia, bulimia, or nausea
No history of allergic reactions attributed to compounds of similar chemical or biologic composition to metformin

No participants with HIV, cirrhosis of any cause, NASH (non-alcoholic steatohepatitis), or hepatitis (auto-immune or infectious)

For participants diagnosed with any other hepatic impairment, consult with protocol principal investigator (PI)
No metabolic acidosis, acute or chronic, including ketoacidosis
No uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements; this includes significant medical conditions including renal failure, hepatic failure, sepsis, and hypoxia
No genetics disorders such as family history of hereditary gastrointestinal polyp disorder (e.g., familial adenomatous polyposis [FAP], hereditary non-polyposis colorectal cancer [HNPCC], Peutz-Jegher disease)
No chronic alcohol use or a history of alcohol abuse (defined as ingestion of >= 3 drinks per day)
No kidney disease or renal insufficiency (defined as serum creatinine outside the normal institutional limits)
Currently on a proton pump inhibitor (PPI) >= 4 weeks (any PPI taken at least once daily is acceptable)
No medication(s) for weight loss ≤ 2 months prior to Pre-Registration
No treatment with medications that may increase metformin hydrochloride levels: cationic drugs, e.g., digoxin, amiloride, procainamide, ranitidine, trimethoprim, quinidine, quinine, vancomycin, triamterene, and morphine
No treatment with other oral hypoglycemic agents
No participant use of metformin, cimetidine (Tagamet), furosemide (Lasix), or nifedipine (Cardizem), or any other drug contraindicated for use with metformin
No receipt of any other investigational agents =< 3 months prior to Pre-Registration, except innocuous agents with no known interaction with the study agent (e.g., standard dose multivitamins or topical agents for limited skin conditions), at the discretion of the Protocol Lead Investigator at each Participating Site

No participants who have undergone ablation or other local therapies (e.g., percutaneous dilatational tracheostomy [PDT], cryotherapy, radiofrequency, argon plasma coagulation [APC], or multipolar electrocoagulation [MPEC])

Patients treated with endoscopic mucosal resection [EMR] allowed
No participants anticipating elective surgery during the study period
No participants planning to undergo elective radiologic studies involving intravascular administration of iodinated contrast materials