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Survival advantage observed with the use of metformin in patients with type II diabetes and colorectal cancer

BACKGROUND: Patients with type II diabetes mellitus (DM) have an increased risk of adenomatous colorectal (CRC) polyps and CRC cancer. The use of the anti-hyperglycemic agent metformin is associated with a reduced incidence of cancer-related deaths. METHODS: We retrospectively evaluated the medical...

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Autores principales: Garrett, C R, Hassabo, H M, Bhadkamkar, N A, Wen, S, Baladandayuthapani, V, Kee, B K, Eng, C, Hassan, M M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326682/
https://www.ncbi.nlm.nih.gov/pubmed/22421948
http://dx.doi.org/10.1038/bjc.2012.71
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author Garrett, C R
Hassabo, H M
Bhadkamkar, N A
Wen, S
Baladandayuthapani, V
Kee, B K
Eng, C
Hassan, M M
author_facet Garrett, C R
Hassabo, H M
Bhadkamkar, N A
Wen, S
Baladandayuthapani, V
Kee, B K
Eng, C
Hassan, M M
author_sort Garrett, C R
collection PubMed
description BACKGROUND: Patients with type II diabetes mellitus (DM) have an increased risk of adenomatous colorectal (CRC) polyps and CRC cancer. The use of the anti-hyperglycemic agent metformin is associated with a reduced incidence of cancer-related deaths. METHODS: We retrospectively evaluated the medical records of 4758 patients seen at a single institution and determined that 424 patients were identified by their physicians as having type II DM and CRC cancer. Data were subsequently acquired determining the subject's age, body mass index (BMI), and disease date of diagnosis, stage, site of cancer, treatment, and survival. RESULTS: Patients with type II DM and CRC cancer treated with metformin as one of their diabetic medications had a survival of 76.9 months (95% CI=61.4–102.4) as compared with 56.9 months in those patients not treated with metformin (95% CI=44.8–68.8), P=0.048. By using a multivariable Cox regression model adjusted for age, sex, race, BMI, and initial stage of disease, we demonstrated that type II diabetic patients treated with metformin had a 30% improvement in overall survival (OS) when compared with diabetic patients treated with other diabetic agents. CONCLUSION: Colorectal cancer patients with DM treated with metformin as part of their diabetic therapy appear to have a superior OS.
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spelling pubmed-33266822013-04-10 Survival advantage observed with the use of metformin in patients with type II diabetes and colorectal cancer Garrett, C R Hassabo, H M Bhadkamkar, N A Wen, S Baladandayuthapani, V Kee, B K Eng, C Hassan, M M Br J Cancer Clinical Study BACKGROUND: Patients with type II diabetes mellitus (DM) have an increased risk of adenomatous colorectal (CRC) polyps and CRC cancer. The use of the anti-hyperglycemic agent metformin is associated with a reduced incidence of cancer-related deaths. METHODS: We retrospectively evaluated the medical records of 4758 patients seen at a single institution and determined that 424 patients were identified by their physicians as having type II DM and CRC cancer. Data were subsequently acquired determining the subject's age, body mass index (BMI), and disease date of diagnosis, stage, site of cancer, treatment, and survival. RESULTS: Patients with type II DM and CRC cancer treated with metformin as one of their diabetic medications had a survival of 76.9 months (95% CI=61.4–102.4) as compared with 56.9 months in those patients not treated with metformin (95% CI=44.8–68.8), P=0.048. By using a multivariable Cox regression model adjusted for age, sex, race, BMI, and initial stage of disease, we demonstrated that type II diabetic patients treated with metformin had a 30% improvement in overall survival (OS) when compared with diabetic patients treated with other diabetic agents. CONCLUSION: Colorectal cancer patients with DM treated with metformin as part of their diabetic therapy appear to have a superior OS. Nature Publishing Group 2012-04-10 2012-03-15 /pmc/articles/PMC3326682/ /pubmed/22421948 http://dx.doi.org/10.1038/bjc.2012.71 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical Study
Garrett, C R
Hassabo, H M
Bhadkamkar, N A
Wen, S
Baladandayuthapani, V
Kee, B K
Eng, C
Hassan, M M
Survival advantage observed with the use of metformin in patients with type II diabetes and colorectal cancer
title Survival advantage observed with the use of metformin in patients with type II diabetes and colorectal cancer
title_full Survival advantage observed with the use of metformin in patients with type II diabetes and colorectal cancer
title_fullStr Survival advantage observed with the use of metformin in patients with type II diabetes and colorectal cancer
title_full_unstemmed Survival advantage observed with the use of metformin in patients with type II diabetes and colorectal cancer
title_short Survival advantage observed with the use of metformin in patients with type II diabetes and colorectal cancer
title_sort survival advantage observed with the use of metformin in patients with type ii diabetes and colorectal cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326682/
https://www.ncbi.nlm.nih.gov/pubmed/22421948
http://dx.doi.org/10.1038/bjc.2012.71
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