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Clinical outcomes of stereotactic body radiotherapy for spinal metastases from hepatocellular carcinoma
PURPOSE: To investigate the outcomes of patients with spinal metastases from hepatocellular carcinoma (HCC), who were treated by stereotactic body radiotherapy (SBRT). MATERIALS AND METHODS: This retrospective study evaluated 23 patients who underwent SBRT from October 2008 to August 2012 for 36 spi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Radiation Oncology
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607575/ https://www.ncbi.nlm.nih.gov/pubmed/26484305 http://dx.doi.org/10.3857/roj.2015.33.3.217 |
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author | Lee, Eonju Kim, Tae Gyu Park, Hee Chul Yu, Jeong Il Lim, Do Hoon Nam, Heerim Lee, Hyebin Lee, Joon Hyeok |
author_facet | Lee, Eonju Kim, Tae Gyu Park, Hee Chul Yu, Jeong Il Lim, Do Hoon Nam, Heerim Lee, Hyebin Lee, Joon Hyeok |
author_sort | Lee, Eonju |
collection | PubMed |
description | PURPOSE: To investigate the outcomes of patients with spinal metastases from hepatocellular carcinoma (HCC), who were treated by stereotactic body radiotherapy (SBRT). MATERIALS AND METHODS: This retrospective study evaluated 23 patients who underwent SBRT from October 2008 to August 2012 for 36 spinal metastases from HCC. SBRT consisted of approximately 2 fractionation schedules, which were 18 to 40 Gy in 1 to 4 fractions for group A lesions (n = 15) and 50 Gy in 10 fractions for group B lesions (n = 21). RESULTS: The median follow-up period was 7 months (range, 2 to 16 months). Seven patients developed grade 1 or 2 gastrointestinal toxicity, and one developed grade 2 leucopenia. Compression fractures occurred in association with 25% of the lesions, with a median time to fracture of 2 months. Pain relief occurred in 92.3% and 68.4% of group A and B lesions, respectively. Radiologic response (complete and partial response) occurred in 80.0% and 61.9% of group A and B lesions, respectively. The estimated 1-year spinal-tumor progression-free survival rate was 78.5%. The median overall survival period and 1-year overall survival rate were 9 months (range, 2 to 16 months) and 25.7%, respectively. CONCLUSION: SBRT for spinal metastases from HCC is well tolerated and effective at providing pain relief and radiologic response. Because compression fractures develop at a high rate following SBRT for spinal metastases from primary HCC, careful follow up of the patient is required. |
format | Online Article Text |
id | pubmed-4607575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Korean Society for Radiation Oncology |
record_format | MEDLINE/PubMed |
spelling | pubmed-46075752015-10-19 Clinical outcomes of stereotactic body radiotherapy for spinal metastases from hepatocellular carcinoma Lee, Eonju Kim, Tae Gyu Park, Hee Chul Yu, Jeong Il Lim, Do Hoon Nam, Heerim Lee, Hyebin Lee, Joon Hyeok Radiat Oncol J Original Article PURPOSE: To investigate the outcomes of patients with spinal metastases from hepatocellular carcinoma (HCC), who were treated by stereotactic body radiotherapy (SBRT). MATERIALS AND METHODS: This retrospective study evaluated 23 patients who underwent SBRT from October 2008 to August 2012 for 36 spinal metastases from HCC. SBRT consisted of approximately 2 fractionation schedules, which were 18 to 40 Gy in 1 to 4 fractions for group A lesions (n = 15) and 50 Gy in 10 fractions for group B lesions (n = 21). RESULTS: The median follow-up period was 7 months (range, 2 to 16 months). Seven patients developed grade 1 or 2 gastrointestinal toxicity, and one developed grade 2 leucopenia. Compression fractures occurred in association with 25% of the lesions, with a median time to fracture of 2 months. Pain relief occurred in 92.3% and 68.4% of group A and B lesions, respectively. Radiologic response (complete and partial response) occurred in 80.0% and 61.9% of group A and B lesions, respectively. The estimated 1-year spinal-tumor progression-free survival rate was 78.5%. The median overall survival period and 1-year overall survival rate were 9 months (range, 2 to 16 months) and 25.7%, respectively. CONCLUSION: SBRT for spinal metastases from HCC is well tolerated and effective at providing pain relief and radiologic response. Because compression fractures develop at a high rate following SBRT for spinal metastases from primary HCC, careful follow up of the patient is required. The Korean Society for Radiation Oncology 2015-09 2015-09-30 /pmc/articles/PMC4607575/ /pubmed/26484305 http://dx.doi.org/10.3857/roj.2015.33.3.217 Text en Copyright © 2015. The Korean Society for Radiation Oncology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Eonju Kim, Tae Gyu Park, Hee Chul Yu, Jeong Il Lim, Do Hoon Nam, Heerim Lee, Hyebin Lee, Joon Hyeok Clinical outcomes of stereotactic body radiotherapy for spinal metastases from hepatocellular carcinoma |
title | Clinical outcomes of stereotactic body radiotherapy for spinal metastases from hepatocellular carcinoma |
title_full | Clinical outcomes of stereotactic body radiotherapy for spinal metastases from hepatocellular carcinoma |
title_fullStr | Clinical outcomes of stereotactic body radiotherapy for spinal metastases from hepatocellular carcinoma |
title_full_unstemmed | Clinical outcomes of stereotactic body radiotherapy for spinal metastases from hepatocellular carcinoma |
title_short | Clinical outcomes of stereotactic body radiotherapy for spinal metastases from hepatocellular carcinoma |
title_sort | clinical outcomes of stereotactic body radiotherapy for spinal metastases from hepatocellular carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607575/ https://www.ncbi.nlm.nih.gov/pubmed/26484305 http://dx.doi.org/10.3857/roj.2015.33.3.217 |
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