Pilot Biomarker Modulation Study of Metformin and Omega-3 Fatty Acids in Woman With a History of Early Stage Breast Cancer

Katherine D. Crew1 site in 1 country19 target enrollmentJanuary 22, 2015

ConditionsStage 0 Breast Carcinoma Breast Neoplasms Stage I Breast Carcinoma Stage II Breast Carcinoma Stage III Breast Carcinoma

InterventionsMetformin Omega-3 fatty acids

DrugsMetformin Omega-3 fatty acids

Overview

Phase: Phase 1
Intervention: Metformin
Conditions: Stage 0 Breast Carcinoma
Sponsor: Katherine D. Crew
Enrollment: 19
Locations: 1
Primary Endpoint: Number of participants successfully completing the 1-year intervention
Status: Completed
Last Updated: 3 years ago

Overview Investigators Eligibility Criteria Arms & Interventions Outcomes Sites Similar Trials

Overview

Brief Summary

The purpose of this study is to determine whether it is feasible to give a combination of Metformin and omega-3 fatty acids for one year to women with a history of early stage breast cancer. We will also evaluate whether the metformin and omega-3 fatty acids combination causes changes in breast tissue, blood, and mammograms.

Detailed Description

Metformin is a medication used to treat and prevent diabetes and omega-3 fatty acids has been shown to lower cholesterol and improve cardiovascular health. Research has shown that Metformin and omega-3 fatty acids may also be effective in preventing cancer. In this study, we want to find out what effects, good and/or bad, the Metformin and omega-3 fatty acids combination has on you and your risk of developing a new breast cancer.

Registry

clinicaltrials.gov

Start Date

January 22, 2015

End Date

April 19, 2017

Last Updated

3 years ago

Study Type

Interventional

Study Design

Single Group

Sex

Female

Investigators

Sponsor

Katherine D. Crew

Responsible Party

Sponsor Investigator

Principal Investigator

Katherine D. Crew

Assistant Professor of Medicine and Epidemiology

Columbia University

Eligibility Criteria

Inclusion Criteria

•History of histologically-confirmed stage 0, I, II, or III breast carcinoma without evidence of disease at trial entry. Participants with a resected local recurrence are eligible
•Minimum of 6 months since last chemotherapy, biologic therapy (i.e., trastuzumab), radiation therapy, and/or breast surgery and no evidence of recurrent disease
•Minimum of 6 months since completion of adjuvant tamoxifen (tamoxifen is known to lower mammographic density119-121). Current use of a third generation aromatase inhibitor \[AI\] (i.e., anastrozole, letrozole, exemestane) is permitted provided that the participant has been on a stable dose for the past 6 months
•Age 21 to 75 years. Both pre- and postmenopausal women will be included in this study. We will exclude perimenopausal women, defined as menstrual cycle irregularity (variable cycle length that differs from normal by more than 7 days) and an Follicle-Stimulating Hormone (FSH) greater than 20 mili international units
•Negative serum pregnancy testing
•Normal mammogram of the contralateral breast within the past 12 months, defined as no new suspicious calcifications or other abnormal findings warranting a breast biopsy
•Eastern Cooperative Oncology Group (ECOG) performance status less than 2
•Participants must have normal organ and marrow function within 28 days prior to randomization
•Body mass index (BMI) greater than or equal to 25 kilograms per meter squared or baseline fasting glucose of less than 126 milligrams per deciliter
•Participants must have a baseline mammographic density greater than or equal to 25 percent based upon the Breast Imaging Reporting and Data System (BIRADS) density score of 2, 3, or

Exclusion Criteria

•History of histologically-confirmed bilateral breast cancer
•History of or plans for bilateral mastectomies
•Evidence of metastatic breast cancer
•Prior radiation therapy or implant in the contralateral breast
•Known diabetes (type 1 or 2) or baseline fasting glucose greater than 126 milligrams per deciliter
•Any condition associated with increased risk of metformin-associated lactic acidosis (e.g., congestive heart failure defined as New York Heart Association \[NYHA\] Class III or IV functional status, history of acidosis of any type, intake of 3 or more alcoholic beverages per day on average over the past 6 months)
•Currently taking metformin, sulfonylureas, thiazolidinediones, or insulin for any reason
•History of allergic reactions attributed to compounds of similar chemical or biologic composition to metformin or omega-3 fatty acids
•Receiving hormone replacement therapy, tamoxifen, or raloxifene within 6 months of trial entry
•Participants may not be receiving any other investigational agents for 30 days prior to baseline evaluation and during the study intervention

Arms & Interventions

Main Arm

Open Label- Metformin and Omega-3 fatty acids for 12 months post baseline data collection.

Intervention: Metformin

Main Arm

Open Label- Metformin and Omega-3 fatty acids for 12 months post baseline data collection.

Intervention: Omega-3 fatty acids

Outcomes

Primary Outcomes

Number of participants successfully completing the 1-year intervention

Time Frame: 12 months (approximately)

The primary objective is to assess the safety and feasibility of a one-year intervention of metformin and omega-3 fatty acids in early stage breast cancer patients who completed adjuvant treatment.

Secondary Outcomes

Percent in reduction of mammographic density(baseline, 12 months)
Change in fasting serum insulin microunits per milliliter(baseline, month 3, 6, 9, and 12)
Change in C-peptide nanograms per milliliter(baseline, month 3, 6, 9, and 12)
Change in insulin-like growth factor 1 (IGF-1) nanograms per milliliter(baseline, month 3, 6, 9, and 12)
Change in insulin-like growth factor binding protein 1 (IGFBP-1) nanograms per milliliter(baseline, month 3, 6, 9, and 12)
Change in insulin-like growth factor binding protein 3 (IGFBP-3) milligrams per liter(baseline, month 3, 6, 9, and 12)
Change in fasting serum glucose milligrams per deciliter(baseline, month 3, 6, 9, and 12)
Change in total cholesterol milligrams per deciliter(baseline, month 3, 6, 9, and 12)
Change in high-density lipoprotein (HDL) milligrams per deciliter(baseline, month 3, 6, 9, and 12)
Change in low-density lipoprotein (LDL) milligrams per deciliter(baseline, month 3, 6, 9, and 12)
Change in Leptin microunits per liter(baseline, month 3, 6, 9, and 12)
Change in adiponectin micrograms per milliliter(baseline, month 3, 6, 9, and 12)
Change in serum C-reactive protein milligrams per deciliter(baseline, month 3, 6, 9, and 12)
Change in Interleukin-6 picograms per milliliter(baseline, month 3, 6, 9, and 12)
Change in body mass index (BMI)(baseline, month 3, 6, 9, and 12)
Change in systolic blood pressure(baseline, month 3, 6, 9, and 12)
Change in diastolic blood pressure(baseline, month 3, 6, 9, and 12)
Change in homeostatus model assessment (HOMA) score(baseline, month 3, 6, 9, and 12)