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Recurrence patterns in patients with high-grade glioma following temozolomide-based chemoradiotherapy
There is currently no consensus regarding the optimal radiation volume for high-grade glioma (HGG). The brain volume irradiated is associated with the extent of radiation neurotoxicity. When reducing the treatment volume, the risk of geographic tumor miss should be considered. In such cases, the rec...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950878/ https://www.ncbi.nlm.nih.gov/pubmed/27446566 http://dx.doi.org/10.3892/mco.2016.936 |
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author | Zhou, Xiaofeng Liao, Xiaofang Zhang, Bicheng He, Huijuan Shui, Yongjie Xu, Wenhong Jiang, Chaogen Shen, Li Wei, Qichun |
author_facet | Zhou, Xiaofeng Liao, Xiaofang Zhang, Bicheng He, Huijuan Shui, Yongjie Xu, Wenhong Jiang, Chaogen Shen, Li Wei, Qichun |
author_sort | Zhou, Xiaofeng |
collection | PubMed |
description | There is currently no consensus regarding the optimal radiation volume for high-grade glioma (HGG). The brain volume irradiated is associated with the extent of radiation neurotoxicity. When reducing the treatment volume, the risk of geographic tumor miss should be considered. In such cases, the recurrence patterns and, particularly, the rate of marginal tumor recurrence, are important indices for determining the optimal radiation volume. In the present study, a smaller-target delineation protocol with limited margins was adopted. The postoperative enhancing tumor and resection cavity were defined as gross tumor volume (GTV); 1 and 2 cm were added to the GTV to create clinical target volume (CTV1 and CTV2), which received 60 and 54 Gy, respectively. At a median follow-up of 14 months, 54 HGG patients developed tumor recurrence. The median overall and progression-free survival were 14 and 10.5 months, respectively. A total of 34 patients developed central recurrence, 8 presented with in-field recurrence, 2 developed marginal recurrence, 2 had distant recurrence and 11 patients developed cerebrospinal fluid dissemination, 2 of whom developed central recurrence, with 1 patient simultaneously developing marginal recurrence. Local recurrence (central and in-field) was found to be the main recurrence pattern. As the rate of marginal recurrence was low (<5%), it appears that the smaller irradiated volume in the present study was appropriate. However, clinical trials investigating limited irradiation volume are required to validate our findings. |
format | Online Article Text |
id | pubmed-4950878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-49508782016-07-21 Recurrence patterns in patients with high-grade glioma following temozolomide-based chemoradiotherapy Zhou, Xiaofeng Liao, Xiaofang Zhang, Bicheng He, Huijuan Shui, Yongjie Xu, Wenhong Jiang, Chaogen Shen, Li Wei, Qichun Mol Clin Oncol Articles There is currently no consensus regarding the optimal radiation volume for high-grade glioma (HGG). The brain volume irradiated is associated with the extent of radiation neurotoxicity. When reducing the treatment volume, the risk of geographic tumor miss should be considered. In such cases, the recurrence patterns and, particularly, the rate of marginal tumor recurrence, are important indices for determining the optimal radiation volume. In the present study, a smaller-target delineation protocol with limited margins was adopted. The postoperative enhancing tumor and resection cavity were defined as gross tumor volume (GTV); 1 and 2 cm were added to the GTV to create clinical target volume (CTV1 and CTV2), which received 60 and 54 Gy, respectively. At a median follow-up of 14 months, 54 HGG patients developed tumor recurrence. The median overall and progression-free survival were 14 and 10.5 months, respectively. A total of 34 patients developed central recurrence, 8 presented with in-field recurrence, 2 developed marginal recurrence, 2 had distant recurrence and 11 patients developed cerebrospinal fluid dissemination, 2 of whom developed central recurrence, with 1 patient simultaneously developing marginal recurrence. Local recurrence (central and in-field) was found to be the main recurrence pattern. As the rate of marginal recurrence was low (<5%), it appears that the smaller irradiated volume in the present study was appropriate. However, clinical trials investigating limited irradiation volume are required to validate our findings. D.A. Spandidos 2016-08 2016-06-15 /pmc/articles/PMC4950878/ /pubmed/27446566 http://dx.doi.org/10.3892/mco.2016.936 Text en Copyright: © Zhou et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Zhou, Xiaofeng Liao, Xiaofang Zhang, Bicheng He, Huijuan Shui, Yongjie Xu, Wenhong Jiang, Chaogen Shen, Li Wei, Qichun Recurrence patterns in patients with high-grade glioma following temozolomide-based chemoradiotherapy |
title | Recurrence patterns in patients with high-grade glioma following temozolomide-based chemoradiotherapy |
title_full | Recurrence patterns in patients with high-grade glioma following temozolomide-based chemoradiotherapy |
title_fullStr | Recurrence patterns in patients with high-grade glioma following temozolomide-based chemoradiotherapy |
title_full_unstemmed | Recurrence patterns in patients with high-grade glioma following temozolomide-based chemoradiotherapy |
title_short | Recurrence patterns in patients with high-grade glioma following temozolomide-based chemoradiotherapy |
title_sort | recurrence patterns in patients with high-grade glioma following temozolomide-based chemoradiotherapy |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950878/ https://www.ncbi.nlm.nih.gov/pubmed/27446566 http://dx.doi.org/10.3892/mco.2016.936 |
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