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The association of diabetes and anti-diabetic medications with clinical outcomes in multiple myeloma

BACKGROUND: Insulin/insulin-like growth factor-1 signalling may underlie the promoting effect of type 2 diabetes on cancer. This study examined the association of diabetes, including steroid-induced diabetes (SID), and the impact of anti-diabetic medication on clinical outcomes of multiple myeloma (...

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Autores principales: Wu, W, Merriman, K, Nabaah, A, Seval, N, Seval, D, Lin, H, Wang, M, Qazilbash, M H, Baladandayuthapani, V, Berry, D, Orlowski, R Z, Lee, M-H, Yeung, S-C J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4119980/
https://www.ncbi.nlm.nih.gov/pubmed/24921909
http://dx.doi.org/10.1038/bjc.2014.307
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author Wu, W
Merriman, K
Nabaah, A
Seval, N
Seval, D
Lin, H
Wang, M
Qazilbash, M H
Baladandayuthapani, V
Berry, D
Orlowski, R Z
Lee, M-H
Yeung, S-C J
author_facet Wu, W
Merriman, K
Nabaah, A
Seval, N
Seval, D
Lin, H
Wang, M
Qazilbash, M H
Baladandayuthapani, V
Berry, D
Orlowski, R Z
Lee, M-H
Yeung, S-C J
author_sort Wu, W
collection PubMed
description BACKGROUND: Insulin/insulin-like growth factor-1 signalling may underlie the promoting effect of type 2 diabetes on cancer. This study examined the association of diabetes, including steroid-induced diabetes (SID), and the impact of anti-diabetic medication on clinical outcomes of multiple myeloma (MM). METHODS: A retrospective review was conducted of 1240 MM patients. Overall survival (OS) and MM disease status prior to death were analysed. RESULTS: Diabetic patients had a significantly shorter OS than non-diabetic patients (median: 65.4 vs 98.7 months). In multivariate analysis, SID was a significant predictor of decreased OS, along with age, comorbidity, MM stage, and cytogenetic abnormalities. Analyzing only the diabetic MM patients, Cox regression showed that metformin predicted an increased OS, whereas use of insulin/analogues predicted a decreased OS. Competing risk analysis showed that DM was associated with increased cumulative incidence of death with progressive MM. Among the diabetics, multivariate regression showed that insulin/analogues were associated with increased, but metformin with decreased death with progressive MM. Potential immortal time bias was evaluated by landmark analyses. CONCLUSIONS: DM, SID in particular, is associated with poor clinical outcomes in MM. Insulin/analogues are associated with poor outcomes, whereas metformin is associated with improved outcomes. No conclusion about causal relationships can be made at this time. Managing hyperglycaemia with non-insulin regimens should be investigated in randomised trials.
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spelling pubmed-41199802015-07-29 The association of diabetes and anti-diabetic medications with clinical outcomes in multiple myeloma Wu, W Merriman, K Nabaah, A Seval, N Seval, D Lin, H Wang, M Qazilbash, M H Baladandayuthapani, V Berry, D Orlowski, R Z Lee, M-H Yeung, S-C J Br J Cancer Epidemiology BACKGROUND: Insulin/insulin-like growth factor-1 signalling may underlie the promoting effect of type 2 diabetes on cancer. This study examined the association of diabetes, including steroid-induced diabetes (SID), and the impact of anti-diabetic medication on clinical outcomes of multiple myeloma (MM). METHODS: A retrospective review was conducted of 1240 MM patients. Overall survival (OS) and MM disease status prior to death were analysed. RESULTS: Diabetic patients had a significantly shorter OS than non-diabetic patients (median: 65.4 vs 98.7 months). In multivariate analysis, SID was a significant predictor of decreased OS, along with age, comorbidity, MM stage, and cytogenetic abnormalities. Analyzing only the diabetic MM patients, Cox regression showed that metformin predicted an increased OS, whereas use of insulin/analogues predicted a decreased OS. Competing risk analysis showed that DM was associated with increased cumulative incidence of death with progressive MM. Among the diabetics, multivariate regression showed that insulin/analogues were associated with increased, but metformin with decreased death with progressive MM. Potential immortal time bias was evaluated by landmark analyses. CONCLUSIONS: DM, SID in particular, is associated with poor clinical outcomes in MM. Insulin/analogues are associated with poor outcomes, whereas metformin is associated with improved outcomes. No conclusion about causal relationships can be made at this time. Managing hyperglycaemia with non-insulin regimens should be investigated in randomised trials. Nature Publishing Group 2014-07-29 2014-06-12 /pmc/articles/PMC4119980/ /pubmed/24921909 http://dx.doi.org/10.1038/bjc.2014.307 Text en Copyright © 2014 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Epidemiology
Wu, W
Merriman, K
Nabaah, A
Seval, N
Seval, D
Lin, H
Wang, M
Qazilbash, M H
Baladandayuthapani, V
Berry, D
Orlowski, R Z
Lee, M-H
Yeung, S-C J
The association of diabetes and anti-diabetic medications with clinical outcomes in multiple myeloma
title The association of diabetes and anti-diabetic medications with clinical outcomes in multiple myeloma
title_full The association of diabetes and anti-diabetic medications with clinical outcomes in multiple myeloma
title_fullStr The association of diabetes and anti-diabetic medications with clinical outcomes in multiple myeloma
title_full_unstemmed The association of diabetes and anti-diabetic medications with clinical outcomes in multiple myeloma
title_short The association of diabetes and anti-diabetic medications with clinical outcomes in multiple myeloma
title_sort association of diabetes and anti-diabetic medications with clinical outcomes in multiple myeloma
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4119980/
https://www.ncbi.nlm.nih.gov/pubmed/24921909
http://dx.doi.org/10.1038/bjc.2014.307
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