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Standard fractionation intensity modulated radiation therapy (IMRT) of primary and recurrent glioblastoma multiforme

BACKGROUND: Intensity-modulated radiation therapy (IMRT) affords unparalleled capacity to deliver conformal radiation doses to tumors in the central nervous system. However, to date, there are few reported outcomes from using IMRT, either alone or as a boost technique, for standard fractionation rad...

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Detalles Bibliográficos
Autores principales: Fuller, Clifton D, Choi, Mehee, Forthuber, Britta, Wang, Samuel J, Rajagiriyil, Nancy, Salter, Bill J, Fuss, Martin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1939706/
https://www.ncbi.nlm.nih.gov/pubmed/17629934
http://dx.doi.org/10.1186/1748-717X-2-26
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author Fuller, Clifton D
Choi, Mehee
Forthuber, Britta
Wang, Samuel J
Rajagiriyil, Nancy
Salter, Bill J
Fuss, Martin
author_facet Fuller, Clifton D
Choi, Mehee
Forthuber, Britta
Wang, Samuel J
Rajagiriyil, Nancy
Salter, Bill J
Fuss, Martin
author_sort Fuller, Clifton D
collection PubMed
description BACKGROUND: Intensity-modulated radiation therapy (IMRT) affords unparalleled capacity to deliver conformal radiation doses to tumors in the central nervous system. However, to date, there are few reported outcomes from using IMRT, either alone or as a boost technique, for standard fractionation radiotherapy for glioblastoma multiforme (GBM). METHODS: Forty-two patients were treated with IMRT alone (72%) or as a boost (28%) after 3-dimensional conformal radiation therapy (3D-CRT). Thirty-three patients with primary disease and 9 patients with recurrent tumors were included. Thirty-four patients (81%) had surgery, with gross tumor resection in 13 patients (36%); 22 patients (53%) received chemo-radiotherapy. The median total radiation dose for all patients was 60 Gy with a range from 30.6 to 74 Gy. Standard fractions of 1.8 Gy/day to 2.0 Gy/day were utilized. RESULTS: Median survival was 8.7 months, with 37 patients (88%) deceased at last contact. Nonparametric analysis showed no survival difference in IMRT-boost vs. IMRT-only groups. CONCLUSION: While technically feasible, preliminary results suggest delivering standard radiation doses by IMRT did not improve survival outcomes in this series compared to historical controls. In light of this lack of a survival benefit and the costs associated with use of IMRT, future prospective trials are needed to evaluate non-survival endpoints such as quality of life and functional preservation. Short of such evidence, the use of IMRT for treatment of GBM needs to be carefully rationalized.
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spelling pubmed-19397062007-08-03 Standard fractionation intensity modulated radiation therapy (IMRT) of primary and recurrent glioblastoma multiforme Fuller, Clifton D Choi, Mehee Forthuber, Britta Wang, Samuel J Rajagiriyil, Nancy Salter, Bill J Fuss, Martin Radiat Oncol Research BACKGROUND: Intensity-modulated radiation therapy (IMRT) affords unparalleled capacity to deliver conformal radiation doses to tumors in the central nervous system. However, to date, there are few reported outcomes from using IMRT, either alone or as a boost technique, for standard fractionation radiotherapy for glioblastoma multiforme (GBM). METHODS: Forty-two patients were treated with IMRT alone (72%) or as a boost (28%) after 3-dimensional conformal radiation therapy (3D-CRT). Thirty-three patients with primary disease and 9 patients with recurrent tumors were included. Thirty-four patients (81%) had surgery, with gross tumor resection in 13 patients (36%); 22 patients (53%) received chemo-radiotherapy. The median total radiation dose for all patients was 60 Gy with a range from 30.6 to 74 Gy. Standard fractions of 1.8 Gy/day to 2.0 Gy/day were utilized. RESULTS: Median survival was 8.7 months, with 37 patients (88%) deceased at last contact. Nonparametric analysis showed no survival difference in IMRT-boost vs. IMRT-only groups. CONCLUSION: While technically feasible, preliminary results suggest delivering standard radiation doses by IMRT did not improve survival outcomes in this series compared to historical controls. In light of this lack of a survival benefit and the costs associated with use of IMRT, future prospective trials are needed to evaluate non-survival endpoints such as quality of life and functional preservation. Short of such evidence, the use of IMRT for treatment of GBM needs to be carefully rationalized. BioMed Central 2007-07-14 /pmc/articles/PMC1939706/ /pubmed/17629934 http://dx.doi.org/10.1186/1748-717X-2-26 Text en Copyright © 2007 Fuller et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Fuller, Clifton D
Choi, Mehee
Forthuber, Britta
Wang, Samuel J
Rajagiriyil, Nancy
Salter, Bill J
Fuss, Martin
Standard fractionation intensity modulated radiation therapy (IMRT) of primary and recurrent glioblastoma multiforme
title Standard fractionation intensity modulated radiation therapy (IMRT) of primary and recurrent glioblastoma multiforme
title_full Standard fractionation intensity modulated radiation therapy (IMRT) of primary and recurrent glioblastoma multiforme
title_fullStr Standard fractionation intensity modulated radiation therapy (IMRT) of primary and recurrent glioblastoma multiforme
title_full_unstemmed Standard fractionation intensity modulated radiation therapy (IMRT) of primary and recurrent glioblastoma multiforme
title_short Standard fractionation intensity modulated radiation therapy (IMRT) of primary and recurrent glioblastoma multiforme
title_sort standard fractionation intensity modulated radiation therapy (imrt) of primary and recurrent glioblastoma multiforme
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1939706/
https://www.ncbi.nlm.nih.gov/pubmed/17629934
http://dx.doi.org/10.1186/1748-717X-2-26
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