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Inclusion / Exclusion Criteria

DISEASE CHARACTERISTICS:

  • 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
  • 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 of the esophagus (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

PATIENT CHARACTERISTICS:

  • ECOG performance status ≤ 1
  • Hemoglobin ≥ 10 g/dL
  • Leukocytes ≥ 3,000/μL (≥ 2,500/μL for African-American participants)
  • Absolute neutrophil count ≥ 1,500/μL (≥ 1,000/μL for African-American participants)
  • Platelets ≥ 100,000/μL
  • 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 or bulimia
  • 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 above institutional upper limit of normal)
  • No history of other cancer(s) with the following exceptions:
    • Non-melanoma skin cancers
    • Cancer(s) for which diagnosis and treatment was completed ≥ 3 years prior to pre-registration

PRIOR CONCURRENT THERAPY:

  • 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 other oral hypoglycemic agents
  • No participant use of non-study metformin or other biguanides
  • 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
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University of Pennsylvania | Perelman School of Medicine