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High-dose radiotherapy is associated with better local control of bone metastasis from hepatocellular carcinoma
We evaluated the pain and radiologic response, time to progression, and dose-response relationship after palliative radiotherapy for bone metastasis from hepatocellular carcinoma. We retrospectively reviewed the medical records of 91 patients between January 2004 and August 2012. The reviewed medica...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362477/ https://www.ncbi.nlm.nih.gov/pubmed/28146433 http://dx.doi.org/10.18632/oncotarget.14858 |
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author | Jung, In-Hye Yoon, Sang Min Kwak, Jungwon Park, Jin-Hong Song, Si Yeol Lee, Sang-Wook Ahn, Seung Do Choi, Eun Kyung Kim, Jong Hoon |
author_facet | Jung, In-Hye Yoon, Sang Min Kwak, Jungwon Park, Jin-Hong Song, Si Yeol Lee, Sang-Wook Ahn, Seung Do Choi, Eun Kyung Kim, Jong Hoon |
author_sort | Jung, In-Hye |
collection | PubMed |
description | We evaluated the pain and radiologic response, time to progression, and dose-response relationship after palliative radiotherapy for bone metastasis from hepatocellular carcinoma. We retrospectively reviewed the medical records of 91 patients between January 2004 and August 2012. The reviewed medical records included data on changes in pain, local tumor progression, and radiologic response evaluated via follow-up images. The radiologic response was assessed based on the Response Evaluation Criteria In Solid Tumors. The pain response was defined according to the International Bone Metastases Consensus Working Party palliative radiotherapy endpoints. Median radiation dose was 40 Gy (range, 20–66 Gy), with various fraction sizes (range, 2.0–6.0 Gy). Pain response rate was 81.4%. During the follow-up periods, radiologic local tumor progression was found in 42 patients (46.2%). The median time to progression was 14.1 months. When the patients were divided into two groups according to their radiation dose (< 55 Gy(10) vs. ≥ 55 Gy(10)), the pain response rates of the high- and low-dose groups did not differ significantly (p = 0.728). However, the radiologic response rate and the time to progression showed significant differences between the two groups (p = 0.009 and p = 0.018, respectively). With dose escalation, higher radiologic response rates and a longer time to progression were achieved in patients with mass-forming bone metastases from hepatocellular carcinoma. |
format | Online Article Text |
id | pubmed-5362477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53624772017-04-24 High-dose radiotherapy is associated with better local control of bone metastasis from hepatocellular carcinoma Jung, In-Hye Yoon, Sang Min Kwak, Jungwon Park, Jin-Hong Song, Si Yeol Lee, Sang-Wook Ahn, Seung Do Choi, Eun Kyung Kim, Jong Hoon Oncotarget Research Paper We evaluated the pain and radiologic response, time to progression, and dose-response relationship after palliative radiotherapy for bone metastasis from hepatocellular carcinoma. We retrospectively reviewed the medical records of 91 patients between January 2004 and August 2012. The reviewed medical records included data on changes in pain, local tumor progression, and radiologic response evaluated via follow-up images. The radiologic response was assessed based on the Response Evaluation Criteria In Solid Tumors. The pain response was defined according to the International Bone Metastases Consensus Working Party palliative radiotherapy endpoints. Median radiation dose was 40 Gy (range, 20–66 Gy), with various fraction sizes (range, 2.0–6.0 Gy). Pain response rate was 81.4%. During the follow-up periods, radiologic local tumor progression was found in 42 patients (46.2%). The median time to progression was 14.1 months. When the patients were divided into two groups according to their radiation dose (< 55 Gy(10) vs. ≥ 55 Gy(10)), the pain response rates of the high- and low-dose groups did not differ significantly (p = 0.728). However, the radiologic response rate and the time to progression showed significant differences between the two groups (p = 0.009 and p = 0.018, respectively). With dose escalation, higher radiologic response rates and a longer time to progression were achieved in patients with mass-forming bone metastases from hepatocellular carcinoma. Impact Journals LLC 2017-01-27 /pmc/articles/PMC5362477/ /pubmed/28146433 http://dx.doi.org/10.18632/oncotarget.14858 Text en Copyright: © 2017 Jung et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Jung, In-Hye Yoon, Sang Min Kwak, Jungwon Park, Jin-Hong Song, Si Yeol Lee, Sang-Wook Ahn, Seung Do Choi, Eun Kyung Kim, Jong Hoon High-dose radiotherapy is associated with better local control of bone metastasis from hepatocellular carcinoma |
title | High-dose radiotherapy is associated with better local control of bone metastasis from hepatocellular carcinoma |
title_full | High-dose radiotherapy is associated with better local control of bone metastasis from hepatocellular carcinoma |
title_fullStr | High-dose radiotherapy is associated with better local control of bone metastasis from hepatocellular carcinoma |
title_full_unstemmed | High-dose radiotherapy is associated with better local control of bone metastasis from hepatocellular carcinoma |
title_short | High-dose radiotherapy is associated with better local control of bone metastasis from hepatocellular carcinoma |
title_sort | high-dose radiotherapy is associated with better local control of bone metastasis from hepatocellular carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362477/ https://www.ncbi.nlm.nih.gov/pubmed/28146433 http://dx.doi.org/10.18632/oncotarget.14858 |
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