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Epidermal Growth Factor Receptor Is Related to Poor Survival in Glioblastomas: Single-Institution Experience

PURPOSE: There are conflicting results surrounding the prognostic significance of epidermal growth factor receptor (EGFR) status in glioblastoma (GBM) patients. Accordingly, we attempted to assess the influence of EGFR expression on the survival of GBM patients receiving postoperative radiotherapy....

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Autores principales: Choi, Youngmin, Song, Young-Jin, Lee, Hyung-Sik, Hur, Won-Joo, Sung, Ki-Han, Kim, Ki-Uk, Choi, Sun-Seob, Kim, Su-Jin, Kim, Dae-Cheol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521249/
https://www.ncbi.nlm.nih.gov/pubmed/23225805
http://dx.doi.org/10.3349/ymj.2013.54.1.101
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author Choi, Youngmin
Song, Young-Jin
Lee, Hyung-Sik
Hur, Won-Joo
Sung, Ki-Han
Kim, Ki-Uk
Choi, Sun-Seob
Kim, Su-Jin
Kim, Dae-Cheol
author_facet Choi, Youngmin
Song, Young-Jin
Lee, Hyung-Sik
Hur, Won-Joo
Sung, Ki-Han
Kim, Ki-Uk
Choi, Sun-Seob
Kim, Su-Jin
Kim, Dae-Cheol
author_sort Choi, Youngmin
collection PubMed
description PURPOSE: There are conflicting results surrounding the prognostic significance of epidermal growth factor receptor (EGFR) status in glioblastoma (GBM) patients. Accordingly, we attempted to assess the influence of EGFR expression on the survival of GBM patients receiving postoperative radiotherapy. MATERIALS AND METHODS: Thirty three GBM patients who had received surgery and postoperative radiotherapy at our institute, between March 1997 and February 2006, were included. The evaluation of EGFR expression with immunohistochemistry was available for 30 patients. Kaplan-Meier survival analysis and Cox regression were used for statistical analysis. RESULTS: EGFR was expressed in 23 patients (76.7%), and not expressed in seven (23.3%). Survival in EGFR expressing GBM patients was significantly less than that in non-expressing patients (median survival: 12.5 versus 17.5 months, p=0.013). Patients who received more than 60 Gy showed improved survival over those who received up to 60 Gy (median survival: 17.0 versus 9.0 months, p=0.000). Negative EGFR expression and a higher radiation dose were significantly correlated with improved survival on multivariate analysis. Survival rates showed no differences according to age, sex, and surgical extent. CONCLUSION: The expression of EGFR demonstrated a significantly deleterious effect on the survival of GBM patients. Therefore, approaches targeting EGFR should be considered in potential treatment methods for GBM patients, in addition to current management strategies.
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spelling pubmed-35212492013-01-01 Epidermal Growth Factor Receptor Is Related to Poor Survival in Glioblastomas: Single-Institution Experience Choi, Youngmin Song, Young-Jin Lee, Hyung-Sik Hur, Won-Joo Sung, Ki-Han Kim, Ki-Uk Choi, Sun-Seob Kim, Su-Jin Kim, Dae-Cheol Yonsei Med J Original Article PURPOSE: There are conflicting results surrounding the prognostic significance of epidermal growth factor receptor (EGFR) status in glioblastoma (GBM) patients. Accordingly, we attempted to assess the influence of EGFR expression on the survival of GBM patients receiving postoperative radiotherapy. MATERIALS AND METHODS: Thirty three GBM patients who had received surgery and postoperative radiotherapy at our institute, between March 1997 and February 2006, were included. The evaluation of EGFR expression with immunohistochemistry was available for 30 patients. Kaplan-Meier survival analysis and Cox regression were used for statistical analysis. RESULTS: EGFR was expressed in 23 patients (76.7%), and not expressed in seven (23.3%). Survival in EGFR expressing GBM patients was significantly less than that in non-expressing patients (median survival: 12.5 versus 17.5 months, p=0.013). Patients who received more than 60 Gy showed improved survival over those who received up to 60 Gy (median survival: 17.0 versus 9.0 months, p=0.000). Negative EGFR expression and a higher radiation dose were significantly correlated with improved survival on multivariate analysis. Survival rates showed no differences according to age, sex, and surgical extent. CONCLUSION: The expression of EGFR demonstrated a significantly deleterious effect on the survival of GBM patients. Therefore, approaches targeting EGFR should be considered in potential treatment methods for GBM patients, in addition to current management strategies. Yonsei University College of Medicine 2013-01-01 2012-11-28 /pmc/articles/PMC3521249/ /pubmed/23225805 http://dx.doi.org/10.3349/ymj.2013.54.1.101 Text en © Copyright: Yonsei University College of Medicine 2013 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Choi, Youngmin
Song, Young-Jin
Lee, Hyung-Sik
Hur, Won-Joo
Sung, Ki-Han
Kim, Ki-Uk
Choi, Sun-Seob
Kim, Su-Jin
Kim, Dae-Cheol
Epidermal Growth Factor Receptor Is Related to Poor Survival in Glioblastomas: Single-Institution Experience
title Epidermal Growth Factor Receptor Is Related to Poor Survival in Glioblastomas: Single-Institution Experience
title_full Epidermal Growth Factor Receptor Is Related to Poor Survival in Glioblastomas: Single-Institution Experience
title_fullStr Epidermal Growth Factor Receptor Is Related to Poor Survival in Glioblastomas: Single-Institution Experience
title_full_unstemmed Epidermal Growth Factor Receptor Is Related to Poor Survival in Glioblastomas: Single-Institution Experience
title_short Epidermal Growth Factor Receptor Is Related to Poor Survival in Glioblastomas: Single-Institution Experience
title_sort epidermal growth factor receptor is related to poor survival in glioblastomas: single-institution experience
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521249/
https://www.ncbi.nlm.nih.gov/pubmed/23225805
http://dx.doi.org/10.3349/ymj.2013.54.1.101
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