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Survival Analysis of Glioblastoma Multiforme
INTRODUCTION: To evaluate the survival of Glioblastoma Multiforme (GBM). MATERIAL AND METHODS: Patients with a pathological diagnosis of Glioblastoma Multiforme (GBM) between 1 January 1994 and 30 November 2013, were retrospectively reviewed. Inclusion criteria: 1) GBM patients with confirmed pathol...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
West Asia Organization for Cancer Prevention
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249474/ https://www.ncbi.nlm.nih.gov/pubmed/30256068 http://dx.doi.org/10.22034/APJCP.2018.19.9.2613 |
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author | Witthayanuwat, Supapan Pesee, Montien Supaadirek, Chunsri Supakalin, Narudom Thamronganantasakul, Komsan Krusun, Srichai |
author_facet | Witthayanuwat, Supapan Pesee, Montien Supaadirek, Chunsri Supakalin, Narudom Thamronganantasakul, Komsan Krusun, Srichai |
author_sort | Witthayanuwat, Supapan |
collection | PubMed |
description | INTRODUCTION: To evaluate the survival of Glioblastoma Multiforme (GBM). MATERIAL AND METHODS: Patients with a pathological diagnosis of Glioblastoma Multiforme (GBM) between 1 January 1994 and 30 November 2013, were retrospectively reviewed. Inclusion criteria: 1) GBM patients with confirmed pathology, 2) GBM patients were treated by multimodality therapy. Exclusion criteria: 1) GBM patients with unconfirmed pathology, 2) GBM patients with spinal involvement, 3) GBM patients with incomplete data records. Seventy-seven patients were treated by multimodality therapy such as surgery plus post-operative radiotherapy (PORT), post-operative Temozolomide (TMZ) concurrent with radiotherapy (CCRT), post-operative CCRT with adjuvant TMZ. The overall survival was calculated by the Kaplan-Meier method and the log-rank test was used to compare the survival curves. A p-value of ≤ 0.05 was considered to be statistically significant. RESULTS: Seventy-seven patients with a median age of 53 years (range 4-76 years) showed a median survival time (MST) of 12 months. In subgroup analyses, the PORT patients revealed a MST of 11 months and 2 year overall survival (OS) rates were 17.2%, the patients with post-operative CCRT with or without adjuvant TMZ revealed a MST of 23 months and 2 year OS rates were 38.2%. The MST of patients by Recursive Partitioning Analysis (RPA), classifications III, IV, V, VI were 26.8 months, 14.2 months, 9.9 months, and 4.0 months, (p <0.001). CONCLUSIONS: The MST of the patients who had post-operative CCRT with or without adjuvant TMZ was better than the PORT group. The RPA classification can be used to predict survival. Multimodality therapy demonstrated the most effective treatment outcome. Temozolomide might be beneficial for GBM patients in order to increase survival time. |
format | Online Article Text |
id | pubmed-6249474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | West Asia Organization for Cancer Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-62494742018-12-07 Survival Analysis of Glioblastoma Multiforme Witthayanuwat, Supapan Pesee, Montien Supaadirek, Chunsri Supakalin, Narudom Thamronganantasakul, Komsan Krusun, Srichai Asian Pac J Cancer Prev Research Article INTRODUCTION: To evaluate the survival of Glioblastoma Multiforme (GBM). MATERIAL AND METHODS: Patients with a pathological diagnosis of Glioblastoma Multiforme (GBM) between 1 January 1994 and 30 November 2013, were retrospectively reviewed. Inclusion criteria: 1) GBM patients with confirmed pathology, 2) GBM patients were treated by multimodality therapy. Exclusion criteria: 1) GBM patients with unconfirmed pathology, 2) GBM patients with spinal involvement, 3) GBM patients with incomplete data records. Seventy-seven patients were treated by multimodality therapy such as surgery plus post-operative radiotherapy (PORT), post-operative Temozolomide (TMZ) concurrent with radiotherapy (CCRT), post-operative CCRT with adjuvant TMZ. The overall survival was calculated by the Kaplan-Meier method and the log-rank test was used to compare the survival curves. A p-value of ≤ 0.05 was considered to be statistically significant. RESULTS: Seventy-seven patients with a median age of 53 years (range 4-76 years) showed a median survival time (MST) of 12 months. In subgroup analyses, the PORT patients revealed a MST of 11 months and 2 year overall survival (OS) rates were 17.2%, the patients with post-operative CCRT with or without adjuvant TMZ revealed a MST of 23 months and 2 year OS rates were 38.2%. The MST of patients by Recursive Partitioning Analysis (RPA), classifications III, IV, V, VI were 26.8 months, 14.2 months, 9.9 months, and 4.0 months, (p <0.001). CONCLUSIONS: The MST of the patients who had post-operative CCRT with or without adjuvant TMZ was better than the PORT group. The RPA classification can be used to predict survival. Multimodality therapy demonstrated the most effective treatment outcome. Temozolomide might be beneficial for GBM patients in order to increase survival time. West Asia Organization for Cancer Prevention 2018 /pmc/articles/PMC6249474/ /pubmed/30256068 http://dx.doi.org/10.22034/APJCP.2018.19.9.2613 Text en Copyright: © Asian Pacific Journal of Cancer Prevention http://creativecommons.org/licenses/BY-SA/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License |
spellingShingle | Research Article Witthayanuwat, Supapan Pesee, Montien Supaadirek, Chunsri Supakalin, Narudom Thamronganantasakul, Komsan Krusun, Srichai Survival Analysis of Glioblastoma Multiforme |
title | Survival Analysis of Glioblastoma Multiforme |
title_full | Survival Analysis of Glioblastoma Multiforme |
title_fullStr | Survival Analysis of Glioblastoma Multiforme |
title_full_unstemmed | Survival Analysis of Glioblastoma Multiforme |
title_short | Survival Analysis of Glioblastoma Multiforme |
title_sort | survival analysis of glioblastoma multiforme |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249474/ https://www.ncbi.nlm.nih.gov/pubmed/30256068 http://dx.doi.org/10.22034/APJCP.2018.19.9.2613 |
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