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Hypofractionated stereotactic re-irradiation: treatment option in recurrent malignant glioma
BACKGROUND: Hypofractionated stereotactic radiotherapy (HFSRT) is one salvage treatment option in previously irradiated patients with recurrent malignant glioma. We analyzed the results of HFSRT and prognostic factors in a single-institution series. METHODS: Between 1997 and 2003, 19 patients with r...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1156875/ https://www.ncbi.nlm.nih.gov/pubmed/15924621 http://dx.doi.org/10.1186/1471-2407-5-55 |
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author | Vordermark, Dirk Kölbl, Oliver Ruprecht, Klemens Vince, Giles H Bratengeier, Klaus Flentje, Michael |
author_facet | Vordermark, Dirk Kölbl, Oliver Ruprecht, Klemens Vince, Giles H Bratengeier, Klaus Flentje, Michael |
author_sort | Vordermark, Dirk |
collection | PubMed |
description | BACKGROUND: Hypofractionated stereotactic radiotherapy (HFSRT) is one salvage treatment option in previously irradiated patients with recurrent malignant glioma. We analyzed the results of HFSRT and prognostic factors in a single-institution series. METHODS: Between 1997 and 2003, 19 patients with recurrent malignant glioma (14 glioblastoma on most recent histology, 5 anaplastic astrocytoma) were treated with HFSRT. The median interval from post-operative radiotherapy to HFSRT was 19 (range 3–116) months, the median daily single dose 5 (4–10) Gy, the median total dose 30 (20–30) Gy and the median planning target volume 15 (4–70) ml. RESULTS: The median overall survival (OS) was 9.3 (1.9-77.6+) months from the time of HFSRT, 15.4 months for grade III and 7.9 months for grade IV tumors (p = 0.029, log-rank test). Two patients were alive at 34.6 and 77.6 months. OS was longer after a total dose of 30 Gy (11.1 months) than after total doses of <30 Gy (7.4 months; p = 0.051). Of five (26%) reoperations, none was performed for presumed or histologically predominant radiation necrosis. Median time to tumor progression after HFSRT on imaging was 4.9 months (1.3 to 37.3) months. CONCLUSION: HFSRT with conservative total doses of no more than 30 Gy is safe and leads to similar OS times as more aggressive treatment schemes. In individual patients, HFSRT in combination with other salvage treatment modalities, was associated with long-term survival. |
format | Text |
id | pubmed-1156875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-11568752005-06-22 Hypofractionated stereotactic re-irradiation: treatment option in recurrent malignant glioma Vordermark, Dirk Kölbl, Oliver Ruprecht, Klemens Vince, Giles H Bratengeier, Klaus Flentje, Michael BMC Cancer Research Article BACKGROUND: Hypofractionated stereotactic radiotherapy (HFSRT) is one salvage treatment option in previously irradiated patients with recurrent malignant glioma. We analyzed the results of HFSRT and prognostic factors in a single-institution series. METHODS: Between 1997 and 2003, 19 patients with recurrent malignant glioma (14 glioblastoma on most recent histology, 5 anaplastic astrocytoma) were treated with HFSRT. The median interval from post-operative radiotherapy to HFSRT was 19 (range 3–116) months, the median daily single dose 5 (4–10) Gy, the median total dose 30 (20–30) Gy and the median planning target volume 15 (4–70) ml. RESULTS: The median overall survival (OS) was 9.3 (1.9-77.6+) months from the time of HFSRT, 15.4 months for grade III and 7.9 months for grade IV tumors (p = 0.029, log-rank test). Two patients were alive at 34.6 and 77.6 months. OS was longer after a total dose of 30 Gy (11.1 months) than after total doses of <30 Gy (7.4 months; p = 0.051). Of five (26%) reoperations, none was performed for presumed or histologically predominant radiation necrosis. Median time to tumor progression after HFSRT on imaging was 4.9 months (1.3 to 37.3) months. CONCLUSION: HFSRT with conservative total doses of no more than 30 Gy is safe and leads to similar OS times as more aggressive treatment schemes. In individual patients, HFSRT in combination with other salvage treatment modalities, was associated with long-term survival. BioMed Central 2005-05-30 /pmc/articles/PMC1156875/ /pubmed/15924621 http://dx.doi.org/10.1186/1471-2407-5-55 Text en Copyright © 2005 Vordermark et al; licensee BioMed Central Ltd. |
spellingShingle | Research Article Vordermark, Dirk Kölbl, Oliver Ruprecht, Klemens Vince, Giles H Bratengeier, Klaus Flentje, Michael Hypofractionated stereotactic re-irradiation: treatment option in recurrent malignant glioma |
title | Hypofractionated stereotactic re-irradiation: treatment option in recurrent malignant glioma |
title_full | Hypofractionated stereotactic re-irradiation: treatment option in recurrent malignant glioma |
title_fullStr | Hypofractionated stereotactic re-irradiation: treatment option in recurrent malignant glioma |
title_full_unstemmed | Hypofractionated stereotactic re-irradiation: treatment option in recurrent malignant glioma |
title_short | Hypofractionated stereotactic re-irradiation: treatment option in recurrent malignant glioma |
title_sort | hypofractionated stereotactic re-irradiation: treatment option in recurrent malignant glioma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1156875/ https://www.ncbi.nlm.nih.gov/pubmed/15924621 http://dx.doi.org/10.1186/1471-2407-5-55 |
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