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Impact of glycemia on survival of glioblastoma patients treated with radiation and temozolomide

Evidence suggests hyperglycemia is associated with worse outcomes in glioblastoma (GB). This study aims to confirm the association between glycemia during radiotherapy (RT) and temozolomide (TMZ) treatment and overall survival (OS) in patients with newly diagnosed GB. This retrospective study includ...

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Autores principales: Tieu, Minh Thi, Lovblom, Leif E., McNamara, Mairéad G., Mason, Warren, Laperriere, Normand, Millar, Barbara-Ann, Ménard, Cynthia, Kiehl, Tim-Rasmus, Perkins, Bruce A., Chung, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498235/
https://www.ncbi.nlm.nih.gov/pubmed/26015297
http://dx.doi.org/10.1007/s11060-015-1815-0
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author Tieu, Minh Thi
Lovblom, Leif E.
McNamara, Mairéad G.
Mason, Warren
Laperriere, Normand
Millar, Barbara-Ann
Ménard, Cynthia
Kiehl, Tim-Rasmus
Perkins, Bruce A.
Chung, Caroline
author_facet Tieu, Minh Thi
Lovblom, Leif E.
McNamara, Mairéad G.
Mason, Warren
Laperriere, Normand
Millar, Barbara-Ann
Ménard, Cynthia
Kiehl, Tim-Rasmus
Perkins, Bruce A.
Chung, Caroline
author_sort Tieu, Minh Thi
collection PubMed
description Evidence suggests hyperglycemia is associated with worse outcomes in glioblastoma (GB). This study aims to confirm the association between glycemia during radiotherapy (RT) and temozolomide (TMZ) treatment and overall survival (OS) in patients with newly diagnosed GB. This retrospective study included GB patients treated with RT and TMZ from 2004 to 2011, randomly divided into independent derivation and validation datasets. Time-weighted mean (TWM) glucose and dexamethasone dose were collected from start of RT to 4 weeks after RT. Univariate (UVA) and multivariable (MVA) analyses investigated the association of TWM glucose and other prognostic factors with overall survival (OS). In total, 393 patients with median follow-up of 14 months were analyzed. In the derivation set (n = 196) the median OS was 15 months and median TWM glucose was 6.3 mmol/L. For patients with a TWM glucose ≤6.3 and >6.3 mmol/L, median OS was 16 and 13 months, respectively (p = 0.03). On UVA, TWM glucose, TWM dexamethasone, age, extent of surgery, and performance status were associated with OS. On MVA, TWM glucose remained an independent predictor of OS (p = 0.03) along with TWM dexamethasone, age, and surgery. The validation set (n = 197), with similar baseline characteristics, confirmed that TWM glucose ≤6.3 mmol/L was independently associated with longer OS (p = 0.005). This study demonstrates and validates that glycemia is an independent predictor for survival in GB patients treated with RT and TMZ.
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spelling pubmed-44982352015-07-15 Impact of glycemia on survival of glioblastoma patients treated with radiation and temozolomide Tieu, Minh Thi Lovblom, Leif E. McNamara, Mairéad G. Mason, Warren Laperriere, Normand Millar, Barbara-Ann Ménard, Cynthia Kiehl, Tim-Rasmus Perkins, Bruce A. Chung, Caroline J Neurooncol Clinical Study Evidence suggests hyperglycemia is associated with worse outcomes in glioblastoma (GB). This study aims to confirm the association between glycemia during radiotherapy (RT) and temozolomide (TMZ) treatment and overall survival (OS) in patients with newly diagnosed GB. This retrospective study included GB patients treated with RT and TMZ from 2004 to 2011, randomly divided into independent derivation and validation datasets. Time-weighted mean (TWM) glucose and dexamethasone dose were collected from start of RT to 4 weeks after RT. Univariate (UVA) and multivariable (MVA) analyses investigated the association of TWM glucose and other prognostic factors with overall survival (OS). In total, 393 patients with median follow-up of 14 months were analyzed. In the derivation set (n = 196) the median OS was 15 months and median TWM glucose was 6.3 mmol/L. For patients with a TWM glucose ≤6.3 and >6.3 mmol/L, median OS was 16 and 13 months, respectively (p = 0.03). On UVA, TWM glucose, TWM dexamethasone, age, extent of surgery, and performance status were associated with OS. On MVA, TWM glucose remained an independent predictor of OS (p = 0.03) along with TWM dexamethasone, age, and surgery. The validation set (n = 197), with similar baseline characteristics, confirmed that TWM glucose ≤6.3 mmol/L was independently associated with longer OS (p = 0.005). This study demonstrates and validates that glycemia is an independent predictor for survival in GB patients treated with RT and TMZ. Springer US 2015-05-27 2015 /pmc/articles/PMC4498235/ /pubmed/26015297 http://dx.doi.org/10.1007/s11060-015-1815-0 Text en © The Author(s) 2015 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.
spellingShingle Clinical Study
Tieu, Minh Thi
Lovblom, Leif E.
McNamara, Mairéad G.
Mason, Warren
Laperriere, Normand
Millar, Barbara-Ann
Ménard, Cynthia
Kiehl, Tim-Rasmus
Perkins, Bruce A.
Chung, Caroline
Impact of glycemia on survival of glioblastoma patients treated with radiation and temozolomide
title Impact of glycemia on survival of glioblastoma patients treated with radiation and temozolomide
title_full Impact of glycemia on survival of glioblastoma patients treated with radiation and temozolomide
title_fullStr Impact of glycemia on survival of glioblastoma patients treated with radiation and temozolomide
title_full_unstemmed Impact of glycemia on survival of glioblastoma patients treated with radiation and temozolomide
title_short Impact of glycemia on survival of glioblastoma patients treated with radiation and temozolomide
title_sort impact of glycemia on survival of glioblastoma patients treated with radiation and temozolomide
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498235/
https://www.ncbi.nlm.nih.gov/pubmed/26015297
http://dx.doi.org/10.1007/s11060-015-1815-0
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