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Gamma Knife Surgery as Monotherapy with Clinically Relevant Doses Prolongs Survival in a Human GBM Xenograft Model
Object. Gamma knife surgery (GKS) may be used for recurring glioblastomas (GBMs). However, patients have then usually undergone multimodal treatment, which makes it difficult to specifically validate GKS independent of established treatments. Thus, we developed an experimental brain tumor model to a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842058/ https://www.ncbi.nlm.nih.gov/pubmed/24312904 http://dx.doi.org/10.1155/2013/139674 |
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author | Sandvei Skeie, Bente Wang, Jian Dodoo, Ernest Heggdal, Jan Ingeman Grønli, Janne Sleire, Linda Bragstad, Sidsel Ganz, Jeremy C. Chekenya, Martha Mørk, Sverre Pedersen, Paal-Henning Enger, Per Øyvind |
author_facet | Sandvei Skeie, Bente Wang, Jian Dodoo, Ernest Heggdal, Jan Ingeman Grønli, Janne Sleire, Linda Bragstad, Sidsel Ganz, Jeremy C. Chekenya, Martha Mørk, Sverre Pedersen, Paal-Henning Enger, Per Øyvind |
author_sort | Sandvei Skeie, Bente |
collection | PubMed |
description | Object. Gamma knife surgery (GKS) may be used for recurring glioblastomas (GBMs). However, patients have then usually undergone multimodal treatment, which makes it difficult to specifically validate GKS independent of established treatments. Thus, we developed an experimental brain tumor model to assess the efficacy and radiotoxicity associated with GKS. Methods. GBM xenografts were implanted intracerebrally in nude rats, and engraftment was confirmed with MRI. The rats were allocated to GKS, with margin doses of 12 Gy or 18 Gy, or to no treatment. Survival time was recorded, tumor sections were examined, and radiotoxicity was evaluated in a behavioral open field test. Results. In the first series, survival from the time of implantation was 96 days in treated rats and 72 days in controls (P < 0.001). In a second experiment, survival was 72 days in the treatment group versus 54 days in controls (P < 0.006). Polynuclear macrophages and fibrosis was seen in groups subjected to GKS. Untreated rats with GBM xenografts displayed less mobility than GKS-treated animals in the open field test 4 weeks after treatment (P = 0.04). Conclusion. GKS administered with clinically relevant doses prolongs survival in rats harboring GBM xenografts, and the associated toxicity is mild. |
format | Online Article Text |
id | pubmed-3842058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-38420582013-12-05 Gamma Knife Surgery as Monotherapy with Clinically Relevant Doses Prolongs Survival in a Human GBM Xenograft Model Sandvei Skeie, Bente Wang, Jian Dodoo, Ernest Heggdal, Jan Ingeman Grønli, Janne Sleire, Linda Bragstad, Sidsel Ganz, Jeremy C. Chekenya, Martha Mørk, Sverre Pedersen, Paal-Henning Enger, Per Øyvind Biomed Res Int Research Article Object. Gamma knife surgery (GKS) may be used for recurring glioblastomas (GBMs). However, patients have then usually undergone multimodal treatment, which makes it difficult to specifically validate GKS independent of established treatments. Thus, we developed an experimental brain tumor model to assess the efficacy and radiotoxicity associated with GKS. Methods. GBM xenografts were implanted intracerebrally in nude rats, and engraftment was confirmed with MRI. The rats were allocated to GKS, with margin doses of 12 Gy or 18 Gy, or to no treatment. Survival time was recorded, tumor sections were examined, and radiotoxicity was evaluated in a behavioral open field test. Results. In the first series, survival from the time of implantation was 96 days in treated rats and 72 days in controls (P < 0.001). In a second experiment, survival was 72 days in the treatment group versus 54 days in controls (P < 0.006). Polynuclear macrophages and fibrosis was seen in groups subjected to GKS. Untreated rats with GBM xenografts displayed less mobility than GKS-treated animals in the open field test 4 weeks after treatment (P = 0.04). Conclusion. GKS administered with clinically relevant doses prolongs survival in rats harboring GBM xenografts, and the associated toxicity is mild. Hindawi Publishing Corporation 2013 2013-11-10 /pmc/articles/PMC3842058/ /pubmed/24312904 http://dx.doi.org/10.1155/2013/139674 Text en Copyright © 2013 Bente Sandvei Skeie et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sandvei Skeie, Bente Wang, Jian Dodoo, Ernest Heggdal, Jan Ingeman Grønli, Janne Sleire, Linda Bragstad, Sidsel Ganz, Jeremy C. Chekenya, Martha Mørk, Sverre Pedersen, Paal-Henning Enger, Per Øyvind Gamma Knife Surgery as Monotherapy with Clinically Relevant Doses Prolongs Survival in a Human GBM Xenograft Model |
title | Gamma Knife Surgery as Monotherapy with Clinically Relevant Doses Prolongs Survival in a Human GBM Xenograft Model |
title_full | Gamma Knife Surgery as Monotherapy with Clinically Relevant Doses Prolongs Survival in a Human GBM Xenograft Model |
title_fullStr | Gamma Knife Surgery as Monotherapy with Clinically Relevant Doses Prolongs Survival in a Human GBM Xenograft Model |
title_full_unstemmed | Gamma Knife Surgery as Monotherapy with Clinically Relevant Doses Prolongs Survival in a Human GBM Xenograft Model |
title_short | Gamma Knife Surgery as Monotherapy with Clinically Relevant Doses Prolongs Survival in a Human GBM Xenograft Model |
title_sort | gamma knife surgery as monotherapy with clinically relevant doses prolongs survival in a human gbm xenograft model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842058/ https://www.ncbi.nlm.nih.gov/pubmed/24312904 http://dx.doi.org/10.1155/2013/139674 |
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