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Survival as a Function of Nonsteroidal Anti-inflammatory Drug Use in Patients with Glioblastoma
Background Findings of both case control and in vitro investigations suggest that non-steroidal anti-inflammatory drugs (NSAIDs) may play a beneficial role in the occurrence, growth, and subsistence of glioblastoma multiforme (GBM) brain tumor in humans. Objective In the present retrospective cohort...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6235638/ https://www.ncbi.nlm.nih.gov/pubmed/30443448 http://dx.doi.org/10.7759/cureus.3277 |
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author | Bruhns, Ryan P James, Whitney S Torabi, Mohammad Borgstrom, Mark Roussas, Adam Lemole, Michael |
author_facet | Bruhns, Ryan P James, Whitney S Torabi, Mohammad Borgstrom, Mark Roussas, Adam Lemole, Michael |
author_sort | Bruhns, Ryan P |
collection | PubMed |
description | Background Findings of both case control and in vitro investigations suggest that non-steroidal anti-inflammatory drugs (NSAIDs) may play a beneficial role in the occurrence, growth, and subsistence of glioblastoma multiforme (GBM) brain tumor in humans. Objective In the present retrospective cohort study, we assessed the impact of NSAID use on survival in patients diagnosed with and treated for GBM brain tumors. Methods The impact of NSAID use and six other potential prognostic indicators of survival were assessed in 71 patients treated for GBM brain tumors from February 2011 to June 2016. Survival analysis and cross-tabulation analyses were performed to examine the potential relationship between NSAID use and occurrence of intracranial hemorrhage over the course of treatment for GBM. Results Kaplan-Meier analysis revealed no significant difference in survival between patients with and without NSAID use (p = 0.75; 95% CI: 10.12, 18.13). Multiple Cox regression analysis identified only treatment with chemotherapy as imposing any statistically significant effect on survival (Hazard Ratio (HR) = 3.31; p < 0.001; 95% CI: 1.80, 6.07). Cross-tabulation revealed no significant effect of NSAID use on occurrence of hemorrhage during treatment, X(2) (2, N = 71) = 0.65, p(2-Sided) = 0.42, (Fisher’s Exact Test: p2-sided = 0.56, p1-sided = 0.31). Conclusion These results suggest that history of NSAID use is not a determinant of survival in GBM patients. More rigorous, prospective investigations of the effect of NSAID use on tumor progression are necessary before the utility of this family of drugs in the treatment of GBM can be adequately appraised. |
format | Online Article Text |
id | pubmed-6235638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-62356382018-11-15 Survival as a Function of Nonsteroidal Anti-inflammatory Drug Use in Patients with Glioblastoma Bruhns, Ryan P James, Whitney S Torabi, Mohammad Borgstrom, Mark Roussas, Adam Lemole, Michael Cureus Preventive Medicine Background Findings of both case control and in vitro investigations suggest that non-steroidal anti-inflammatory drugs (NSAIDs) may play a beneficial role in the occurrence, growth, and subsistence of glioblastoma multiforme (GBM) brain tumor in humans. Objective In the present retrospective cohort study, we assessed the impact of NSAID use on survival in patients diagnosed with and treated for GBM brain tumors. Methods The impact of NSAID use and six other potential prognostic indicators of survival were assessed in 71 patients treated for GBM brain tumors from February 2011 to June 2016. Survival analysis and cross-tabulation analyses were performed to examine the potential relationship between NSAID use and occurrence of intracranial hemorrhage over the course of treatment for GBM. Results Kaplan-Meier analysis revealed no significant difference in survival between patients with and without NSAID use (p = 0.75; 95% CI: 10.12, 18.13). Multiple Cox regression analysis identified only treatment with chemotherapy as imposing any statistically significant effect on survival (Hazard Ratio (HR) = 3.31; p < 0.001; 95% CI: 1.80, 6.07). Cross-tabulation revealed no significant effect of NSAID use on occurrence of hemorrhage during treatment, X(2) (2, N = 71) = 0.65, p(2-Sided) = 0.42, (Fisher’s Exact Test: p2-sided = 0.56, p1-sided = 0.31). Conclusion These results suggest that history of NSAID use is not a determinant of survival in GBM patients. More rigorous, prospective investigations of the effect of NSAID use on tumor progression are necessary before the utility of this family of drugs in the treatment of GBM can be adequately appraised. Cureus 2018-09-10 /pmc/articles/PMC6235638/ /pubmed/30443448 http://dx.doi.org/10.7759/cureus.3277 Text en Copyright © 2018, Bruhns et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Preventive Medicine Bruhns, Ryan P James, Whitney S Torabi, Mohammad Borgstrom, Mark Roussas, Adam Lemole, Michael Survival as a Function of Nonsteroidal Anti-inflammatory Drug Use in Patients with Glioblastoma |
title | Survival as a Function of Nonsteroidal Anti-inflammatory Drug Use in Patients with Glioblastoma |
title_full | Survival as a Function of Nonsteroidal Anti-inflammatory Drug Use in Patients with Glioblastoma |
title_fullStr | Survival as a Function of Nonsteroidal Anti-inflammatory Drug Use in Patients with Glioblastoma |
title_full_unstemmed | Survival as a Function of Nonsteroidal Anti-inflammatory Drug Use in Patients with Glioblastoma |
title_short | Survival as a Function of Nonsteroidal Anti-inflammatory Drug Use in Patients with Glioblastoma |
title_sort | survival as a function of nonsteroidal anti-inflammatory drug use in patients with glioblastoma |
topic | Preventive Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6235638/ https://www.ncbi.nlm.nih.gov/pubmed/30443448 http://dx.doi.org/10.7759/cureus.3277 |
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