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Phase II study of metformin for reduction of obesity-associated breast cancer risk: a randomized controlled trial protocol

BACKGROUND: Two-thirds of U.S. adult women are overweight or obese. High body mass index (BMI) and adult weight gain are risk factors for a number of chronic diseases, including postmenopausal breast cancer. The higher postmenopausal breast cancer risk in women with elevated BMI is likely to be attr...

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Autores principales: Martinez, Jessica A., Chalasani, Pavani, Thomson, Cynthia A., Roe, Denise, Altbach, Maria, Galons, Jean-Philippe, Stopeck, Alison, Thompson, Patricia A., Villa-Guillen, Diana Evelyn, Chow, H-H. Sherry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950218/
https://www.ncbi.nlm.nih.gov/pubmed/27430256
http://dx.doi.org/10.1186/s12885-016-2551-3
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author Martinez, Jessica A.
Chalasani, Pavani
Thomson, Cynthia A.
Roe, Denise
Altbach, Maria
Galons, Jean-Philippe
Stopeck, Alison
Thompson, Patricia A.
Villa-Guillen, Diana Evelyn
Chow, H-H. Sherry
author_facet Martinez, Jessica A.
Chalasani, Pavani
Thomson, Cynthia A.
Roe, Denise
Altbach, Maria
Galons, Jean-Philippe
Stopeck, Alison
Thompson, Patricia A.
Villa-Guillen, Diana Evelyn
Chow, H-H. Sherry
author_sort Martinez, Jessica A.
collection PubMed
description BACKGROUND: Two-thirds of U.S. adult women are overweight or obese. High body mass index (BMI) and adult weight gain are risk factors for a number of chronic diseases, including postmenopausal breast cancer. The higher postmenopausal breast cancer risk in women with elevated BMI is likely to be attributable to related metabolic disturbances including altered circulating sex steroid hormones and adipokines, elevated pro-inflammatory cytokines, and insulin resistance. Metformin is a widely used antidiabetic drug that has demonstrated favorable effects on metabolic disturbances and as such may lead to lower breast cancer risk in obese women. Further, the anti-proliferative effects of metformin suggest it may decrease breast density, an accepted biomarker of breast cancer risk. METHODS/DESIGN: This is a Phase II randomized, double-blind, placebo-controlled trial of metformin in overweight/obese premenopausal women who have elements of metabolic syndrome. Eligible participants will be randomized to receive metformin 850 mg BID (n = 75) or placebo (n = 75) for 12 months. The primary endpoint is change in breast density, based on magnetic resonance imaging (MRI) acquired fat-water features. Secondary outcomes include changes in serum insulin levels, serum insulin-like growth factor (IGF)-1 to insulin-like growth factor binding protein (IGFBP)-3 ratio, serum IGF-2 levels, serum testosterone levels, serum leptin to adiponectin ratio, body weight, and waist circumference. Exploratory outcomes include changes in metabolomic profiles in plasma and nipple aspirate fluid. Changes in tissue architecture as well as cellular and molecular targets in breast tissue collected in a subgroup of participants will also be explored. DISCUSSION: The study will evaluate whether metformin can result in favorable changes in breast density, select proteins and hormones, products of body metabolism, and body weight and composition. The study should help determine the potential breast cancer preventive activity of metformin in a growing population at risk for multiple diseases. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02028221. Registered on January 2, 2014. Grant #: 1R01CA172444-01A1 awarded on Sept 11, 2013.
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spelling pubmed-49502182016-07-20 Phase II study of metformin for reduction of obesity-associated breast cancer risk: a randomized controlled trial protocol Martinez, Jessica A. Chalasani, Pavani Thomson, Cynthia A. Roe, Denise Altbach, Maria Galons, Jean-Philippe Stopeck, Alison Thompson, Patricia A. Villa-Guillen, Diana Evelyn Chow, H-H. Sherry BMC Cancer Study Protocol BACKGROUND: Two-thirds of U.S. adult women are overweight or obese. High body mass index (BMI) and adult weight gain are risk factors for a number of chronic diseases, including postmenopausal breast cancer. The higher postmenopausal breast cancer risk in women with elevated BMI is likely to be attributable to related metabolic disturbances including altered circulating sex steroid hormones and adipokines, elevated pro-inflammatory cytokines, and insulin resistance. Metformin is a widely used antidiabetic drug that has demonstrated favorable effects on metabolic disturbances and as such may lead to lower breast cancer risk in obese women. Further, the anti-proliferative effects of metformin suggest it may decrease breast density, an accepted biomarker of breast cancer risk. METHODS/DESIGN: This is a Phase II randomized, double-blind, placebo-controlled trial of metformin in overweight/obese premenopausal women who have elements of metabolic syndrome. Eligible participants will be randomized to receive metformin 850 mg BID (n = 75) or placebo (n = 75) for 12 months. The primary endpoint is change in breast density, based on magnetic resonance imaging (MRI) acquired fat-water features. Secondary outcomes include changes in serum insulin levels, serum insulin-like growth factor (IGF)-1 to insulin-like growth factor binding protein (IGFBP)-3 ratio, serum IGF-2 levels, serum testosterone levels, serum leptin to adiponectin ratio, body weight, and waist circumference. Exploratory outcomes include changes in metabolomic profiles in plasma and nipple aspirate fluid. Changes in tissue architecture as well as cellular and molecular targets in breast tissue collected in a subgroup of participants will also be explored. DISCUSSION: The study will evaluate whether metformin can result in favorable changes in breast density, select proteins and hormones, products of body metabolism, and body weight and composition. The study should help determine the potential breast cancer preventive activity of metformin in a growing population at risk for multiple diseases. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02028221. Registered on January 2, 2014. Grant #: 1R01CA172444-01A1 awarded on Sept 11, 2013. BioMed Central 2016-07-19 /pmc/articles/PMC4950218/ /pubmed/27430256 http://dx.doi.org/10.1186/s12885-016-2551-3 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Martinez, Jessica A.
Chalasani, Pavani
Thomson, Cynthia A.
Roe, Denise
Altbach, Maria
Galons, Jean-Philippe
Stopeck, Alison
Thompson, Patricia A.
Villa-Guillen, Diana Evelyn
Chow, H-H. Sherry
Phase II study of metformin for reduction of obesity-associated breast cancer risk: a randomized controlled trial protocol
title Phase II study of metformin for reduction of obesity-associated breast cancer risk: a randomized controlled trial protocol
title_full Phase II study of metformin for reduction of obesity-associated breast cancer risk: a randomized controlled trial protocol
title_fullStr Phase II study of metformin for reduction of obesity-associated breast cancer risk: a randomized controlled trial protocol
title_full_unstemmed Phase II study of metformin for reduction of obesity-associated breast cancer risk: a randomized controlled trial protocol
title_short Phase II study of metformin for reduction of obesity-associated breast cancer risk: a randomized controlled trial protocol
title_sort phase ii study of metformin for reduction of obesity-associated breast cancer risk: a randomized controlled trial protocol
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950218/
https://www.ncbi.nlm.nih.gov/pubmed/27430256
http://dx.doi.org/10.1186/s12885-016-2551-3
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