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The effect of metformin on breast cancer outcomes in patients with type 2 diabetes
Observational data suggest that metformin use decreases breast cancer (BC) incidence in women with diabetes; the impact of metformin on BC outcomes in this population is less clear. The purpose of this analysis was to explore whether metformin use influences BC outcomes in women with type 2 diabetes...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303170/ https://www.ncbi.nlm.nih.gov/pubmed/24944108 http://dx.doi.org/10.1002/cam4.259 |
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author | Oppong, Bridget A Pharmer, Lindsay A Oskar, Sabine Eaton, Anne Stempel, Michelle Patil, Sujata King, Tari A |
author_facet | Oppong, Bridget A Pharmer, Lindsay A Oskar, Sabine Eaton, Anne Stempel, Michelle Patil, Sujata King, Tari A |
author_sort | Oppong, Bridget A |
collection | PubMed |
description | Observational data suggest that metformin use decreases breast cancer (BC) incidence in women with diabetes; the impact of metformin on BC outcomes in this population is less clear. The purpose of this analysis was to explore whether metformin use influences BC outcomes in women with type 2 diabetes. Prospective institutional databases were reviewed to identify patients with diabetes who received chemotherapy for stages I–III BC from 2000 to 2005. Patients diagnosed with diabetes before or within 6 months of BC diagnosis were included. Males and those with type I, gestational, or steroid-induced diabetes were excluded. Patients were stratified based on metformin use, at baseline, defined as use at time of BC diagnosis or at diabetes diagnosis if within 6 months of BC diagnosis. Kaplan–Meier methods were used to estimate rates of recurrence-free survival (RFS), overall survival (OS), and contralateral breast cancer (CBC). We identified 313 patients with diabetes who received chemotherapy for BC, 141 (45%) fulfilled inclusion criteria and 76 (54%) used metformin at baseline. There were no differences in clinical presentation or tumor characteristics between metformin users and nonusers. At a median follow-up of 87 months (range, 6.9–140.4 months), there was no difference in RFS (P = 0.61), OS (P = 0.462), or CBC (P = 0.156) based on metformin use. Five-year RFS was 90.4% (95% CI, 84–97) in metformin users and 85.4% (95% CI, 78–94) in nonusers. In this cohort of patients with type 2 diabetes receiving systemic chemotherapy for invasive BC, the use of metformin was not associated with improved outcomes. |
format | Online Article Text |
id | pubmed-4303170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43031702015-01-22 The effect of metformin on breast cancer outcomes in patients with type 2 diabetes Oppong, Bridget A Pharmer, Lindsay A Oskar, Sabine Eaton, Anne Stempel, Michelle Patil, Sujata King, Tari A Cancer Med Clinical Cancer Research Observational data suggest that metformin use decreases breast cancer (BC) incidence in women with diabetes; the impact of metformin on BC outcomes in this population is less clear. The purpose of this analysis was to explore whether metformin use influences BC outcomes in women with type 2 diabetes. Prospective institutional databases were reviewed to identify patients with diabetes who received chemotherapy for stages I–III BC from 2000 to 2005. Patients diagnosed with diabetes before or within 6 months of BC diagnosis were included. Males and those with type I, gestational, or steroid-induced diabetes were excluded. Patients were stratified based on metformin use, at baseline, defined as use at time of BC diagnosis or at diabetes diagnosis if within 6 months of BC diagnosis. Kaplan–Meier methods were used to estimate rates of recurrence-free survival (RFS), overall survival (OS), and contralateral breast cancer (CBC). We identified 313 patients with diabetes who received chemotherapy for BC, 141 (45%) fulfilled inclusion criteria and 76 (54%) used metformin at baseline. There were no differences in clinical presentation or tumor characteristics between metformin users and nonusers. At a median follow-up of 87 months (range, 6.9–140.4 months), there was no difference in RFS (P = 0.61), OS (P = 0.462), or CBC (P = 0.156) based on metformin use. Five-year RFS was 90.4% (95% CI, 84–97) in metformin users and 85.4% (95% CI, 78–94) in nonusers. In this cohort of patients with type 2 diabetes receiving systemic chemotherapy for invasive BC, the use of metformin was not associated with improved outcomes. BlackWell Publishing Ltd 2014-08 2014-06-18 /pmc/articles/PMC4303170/ /pubmed/24944108 http://dx.doi.org/10.1002/cam4.259 Text en © 2014 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Cancer Research Oppong, Bridget A Pharmer, Lindsay A Oskar, Sabine Eaton, Anne Stempel, Michelle Patil, Sujata King, Tari A The effect of metformin on breast cancer outcomes in patients with type 2 diabetes |
title | The effect of metformin on breast cancer outcomes in patients with type 2 diabetes |
title_full | The effect of metformin on breast cancer outcomes in patients with type 2 diabetes |
title_fullStr | The effect of metformin on breast cancer outcomes in patients with type 2 diabetes |
title_full_unstemmed | The effect of metformin on breast cancer outcomes in patients with type 2 diabetes |
title_short | The effect of metformin on breast cancer outcomes in patients with type 2 diabetes |
title_sort | effect of metformin on breast cancer outcomes in patients with type 2 diabetes |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303170/ https://www.ncbi.nlm.nih.gov/pubmed/24944108 http://dx.doi.org/10.1002/cam4.259 |
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