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Radiosurgery of Spinal Meningiomas and Schwannomas
Purpose of this study is to analyze local control, clinical symptoms and toxicity after image-guided radiosurgery of spinal meningiomas and schwannomas. Standard treatment of benign spinal lesions is microsurgical resection. While a few publications have reported about radiosurgery for benign spinal...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527413/ https://www.ncbi.nlm.nih.gov/pubmed/22181328 http://dx.doi.org/10.7785/tcrt.2012.500231 |
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author | Kufeld, M. Wowra, B. Muacevic, A. Zausinger, Stefan Tonn, Jörg-Christian |
author_facet | Kufeld, M. Wowra, B. Muacevic, A. Zausinger, Stefan Tonn, Jörg-Christian |
author_sort | Kufeld, M. |
collection | PubMed |
description | Purpose of this study is to analyze local control, clinical symptoms and toxicity after image-guided radiosurgery of spinal meningiomas and schwannomas. Standard treatment of benign spinal lesions is microsurgical resection. While a few publications have reported about radiosurgery for benign spinal lesions, this is the first study analyzing the outcome of robotic radiosurgery for benign spinal tumors, treated exclusively with a non-invasive, fiducial free, single-fraction setup. Thirty-six patients with spinal meningiomas or schwannomas were treated, utilizing a robotic radiosurgery system (CyberKnife®, Accuray Inc. Sunnyvale CA), and were followed prospectively. Medical history, histology, clinical symptoms and radiographic outcome were recorded. Thirty-nine spinal lesions were treated because of tumor recurrence, remnants after microsurgery, multiple lesions, or rejection of open surgery. Median age was 45 years (range 18–80 years). Median target volume was 3.4 cm(3) (range 0.2–43.4 cm(3)). Histology revealed 28 schwannomas and 11 meningiomas (WHO grade I). All spinal levels were affected. Median prescription dose was 14 Gray (95% C.I. 13.4–14 Gy) to the 70% isodose. After a median follow-up of 18 months (range 6–50 months) no local tumor progression was detected. 20 lesions (51%) remained stable, 19 tumors (49%) decreased in size. One patient with schwannomatosis was treated repeatedly for three new tumor locations. Pain was the initial symptom in 16 of 25 schwannoma patients, and in 3 of 11 patients with meningiomas. Pain levels decreased in 8/19 patients. All but one patient with motor deficits remained clinically stable. No myelopathic signs where found. Single-session radiosurgery for benign spinal tumors in selected patients has proven to inhibit tumor progression within the observed period without signs of early toxicity. Radiosurgery offers an additional treatment option, if microsurgery is not feasible in cases of tumor recurrence, post-resection remnants, multiple lesions, or medical comorbidity. |
format | Online Article Text |
id | pubmed-4527413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-45274132015-09-25 Radiosurgery of Spinal Meningiomas and Schwannomas Kufeld, M. Wowra, B. Muacevic, A. Zausinger, Stefan Tonn, Jörg-Christian Technol Cancer Res Treat Articles Purpose of this study is to analyze local control, clinical symptoms and toxicity after image-guided radiosurgery of spinal meningiomas and schwannomas. Standard treatment of benign spinal lesions is microsurgical resection. While a few publications have reported about radiosurgery for benign spinal lesions, this is the first study analyzing the outcome of robotic radiosurgery for benign spinal tumors, treated exclusively with a non-invasive, fiducial free, single-fraction setup. Thirty-six patients with spinal meningiomas or schwannomas were treated, utilizing a robotic radiosurgery system (CyberKnife®, Accuray Inc. Sunnyvale CA), and were followed prospectively. Medical history, histology, clinical symptoms and radiographic outcome were recorded. Thirty-nine spinal lesions were treated because of tumor recurrence, remnants after microsurgery, multiple lesions, or rejection of open surgery. Median age was 45 years (range 18–80 years). Median target volume was 3.4 cm(3) (range 0.2–43.4 cm(3)). Histology revealed 28 schwannomas and 11 meningiomas (WHO grade I). All spinal levels were affected. Median prescription dose was 14 Gray (95% C.I. 13.4–14 Gy) to the 70% isodose. After a median follow-up of 18 months (range 6–50 months) no local tumor progression was detected. 20 lesions (51%) remained stable, 19 tumors (49%) decreased in size. One patient with schwannomatosis was treated repeatedly for three new tumor locations. Pain was the initial symptom in 16 of 25 schwannoma patients, and in 3 of 11 patients with meningiomas. Pain levels decreased in 8/19 patients. All but one patient with motor deficits remained clinically stable. No myelopathic signs where found. Single-session radiosurgery for benign spinal tumors in selected patients has proven to inhibit tumor progression within the observed period without signs of early toxicity. Radiosurgery offers an additional treatment option, if microsurgery is not feasible in cases of tumor recurrence, post-resection remnants, multiple lesions, or medical comorbidity. SAGE Publications 2012-02 /pmc/articles/PMC4527413/ /pubmed/22181328 http://dx.doi.org/10.7785/tcrt.2012.500231 Text en ©Adenine Press (2012) |
spellingShingle | Articles Kufeld, M. Wowra, B. Muacevic, A. Zausinger, Stefan Tonn, Jörg-Christian Radiosurgery of Spinal Meningiomas and Schwannomas |
title | Radiosurgery of Spinal Meningiomas and Schwannomas |
title_full | Radiosurgery of Spinal Meningiomas and Schwannomas |
title_fullStr | Radiosurgery of Spinal Meningiomas and Schwannomas |
title_full_unstemmed | Radiosurgery of Spinal Meningiomas and Schwannomas |
title_short | Radiosurgery of Spinal Meningiomas and Schwannomas |
title_sort | radiosurgery of spinal meningiomas and schwannomas |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527413/ https://www.ncbi.nlm.nih.gov/pubmed/22181328 http://dx.doi.org/10.7785/tcrt.2012.500231 |
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