Metformin for the Treatment of Insulin Resistance in Women With Stage I-III Breast Cancer Completing Chemotherapy

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexFemale
Age18+
SponsorCity of Hope Medical Center

About this trial

This phase III trial evaluates how often women develop insulin resistance and type-2 diabetes and compares metformin with usual care to usual care alone in treating insulin resistance in women with stage I-III breast cancer after chemotherapy. Insulin resistance occurs when cells stop responding to insulin and is a risk factor for developing diabetes and heart disease. Higher levels of insulin have been shown to be associated with aggressive breast cancer. Metformin hydrochloride decreases the amount of glucose (a type of sugar) released into the bloodstream from the liver and increases the body's use of the glucose. Metformin as well as standard of care diet and exercise education is known to lower blood sugar. However, chemotherapy may accelerate metabolic disorders, such as high blood sugar, and the impact of metformin in these breast cancer survivors is not known. Giving metformin with usual care may be more effective than usual care alone in preventing or reversing insulin resistance in women with stage I-III breast cancer after chemotherapy.

Eligibility criteria

Qualifiers

Documented informed consent of the participant and/or legally authorized representative

Agreement to allow lab draw of approximately 26 mL of blood (less than 2 tablespoons)

To check blood counts, organ function and disease at baseline and 12 months

Review of clinical charts at pre-registration* (refer to Study Calendar), baseline, 3 months, 6 months,12 months, and 24 months

Disqualifiers

Currently taking metformin or any other oral antidiabetic medications. Weight loss medications are permitted - e.g. semaglutide

Taking tamoxifen or aromatase inhibitor

Contraindication to metformin prevention such as acute hypersensitivity or allergic reaction to metformin

Participants with acute or chronic renal insufficiency (a glomerular filtration rate [GFR] < 60 mL/min/1.73m²) or those with acute renal insufficiency of any severity due to hepato-renal syndrome or in the peri-operative liver transplantation period

Trial design

Treatments tested in this trial

  • Biospecimen Collection
  • Educational Intervention
  • Extended Release Metformin Hydrochloride
  • Questionnaire Administration

Treatment groups

80 Participants
are divided into 2 treatment groups

Sponsors and collaborators

City of Hope Medical Center

Lead sponsor

National Cancer Institute (NCI)

Collaborator