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Survival outcomes after stereotactic body radiotherapy for 79 Japanese patients with hepatocellular carcinoma
Stereotactic body radiotherapy (SBRT) is a relatively new treatment for liver tumor. Outcomes of SBRT for liver tumors unsuitable for ablation or surgical resection were evaluated. A total of 79 patients treated with SBRT for primary hepatocellular carcinoma (HCC) between 2004 and 2012 in six Japane...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426924/ https://www.ncbi.nlm.nih.gov/pubmed/25691453 http://dx.doi.org/10.1093/jrr/rru130 |
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author | Yamashita, Hideomi Onishi, Hiroshi Murakami, Naoya Matsumoto, Yasuo Matsuo, Yukinori Nomiya, Takuma Nakagawa, Keiichi |
author_facet | Yamashita, Hideomi Onishi, Hiroshi Murakami, Naoya Matsumoto, Yasuo Matsuo, Yukinori Nomiya, Takuma Nakagawa, Keiichi |
author_sort | Yamashita, Hideomi |
collection | PubMed |
description | Stereotactic body radiotherapy (SBRT) is a relatively new treatment for liver tumor. Outcomes of SBRT for liver tumors unsuitable for ablation or surgical resection were evaluated. A total of 79 patients treated with SBRT for primary hepatocellular carcinoma (HCC) between 2004 and 2012 in six Japanese institutions were studied retrospectively. Patients treated with SBRT preceded by trans-arterial chemoembolization were eligible. Their median age was 73 years, 76% were males, and their Child–Pugh scores were Grades A (85%) and B (11%) before SBRT. The median biologically effective dose (α/β = 10 Gy) was 96.3 Gy. The median follow-up time was 21.0 months for surviving patients. The 2-year overall survival (OS), progression-free survival (PFS), and distant metastasis-free survival were 53%, 40% and 76%, respectively. Sex and serum PIVKA-II values were significant predictive factors for OS. Hypovascular or hypervascular types of HCC, sex and clinical stage were significant predictive factors for PFS. The 2-year PFS was 66% in Stage I vs 18% in Stages II–III. Multivariate analysis indicated that clinical stage was the only significant predictive factor for PFS. No Grade 3 laboratory toxicities in the acute, sub-acute, and chronic phases were observed. PFS after SBRT for liver tumor was satisfactory, especially for Stage I HCC, even though these patients were unsuitable for resection and ablation. SBRT is safe and might be an alternative to resection and ablation. |
format | Online Article Text |
id | pubmed-4426924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44269242015-05-15 Survival outcomes after stereotactic body radiotherapy for 79 Japanese patients with hepatocellular carcinoma Yamashita, Hideomi Onishi, Hiroshi Murakami, Naoya Matsumoto, Yasuo Matsuo, Yukinori Nomiya, Takuma Nakagawa, Keiichi J Radiat Res Oncology Stereotactic body radiotherapy (SBRT) is a relatively new treatment for liver tumor. Outcomes of SBRT for liver tumors unsuitable for ablation or surgical resection were evaluated. A total of 79 patients treated with SBRT for primary hepatocellular carcinoma (HCC) between 2004 and 2012 in six Japanese institutions were studied retrospectively. Patients treated with SBRT preceded by trans-arterial chemoembolization were eligible. Their median age was 73 years, 76% were males, and their Child–Pugh scores were Grades A (85%) and B (11%) before SBRT. The median biologically effective dose (α/β = 10 Gy) was 96.3 Gy. The median follow-up time was 21.0 months for surviving patients. The 2-year overall survival (OS), progression-free survival (PFS), and distant metastasis-free survival were 53%, 40% and 76%, respectively. Sex and serum PIVKA-II values were significant predictive factors for OS. Hypovascular or hypervascular types of HCC, sex and clinical stage were significant predictive factors for PFS. The 2-year PFS was 66% in Stage I vs 18% in Stages II–III. Multivariate analysis indicated that clinical stage was the only significant predictive factor for PFS. No Grade 3 laboratory toxicities in the acute, sub-acute, and chronic phases were observed. PFS after SBRT for liver tumor was satisfactory, especially for Stage I HCC, even though these patients were unsuitable for resection and ablation. SBRT is safe and might be an alternative to resection and ablation. Oxford University Press 2015-05 2015-02-16 /pmc/articles/PMC4426924/ /pubmed/25691453 http://dx.doi.org/10.1093/jrr/rru130 Text en © The Author 2015. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Oncology Yamashita, Hideomi Onishi, Hiroshi Murakami, Naoya Matsumoto, Yasuo Matsuo, Yukinori Nomiya, Takuma Nakagawa, Keiichi Survival outcomes after stereotactic body radiotherapy for 79 Japanese patients with hepatocellular carcinoma |
title | Survival outcomes after stereotactic body radiotherapy for 79 Japanese patients with hepatocellular carcinoma |
title_full | Survival outcomes after stereotactic body radiotherapy for 79 Japanese patients with hepatocellular carcinoma |
title_fullStr | Survival outcomes after stereotactic body radiotherapy for 79 Japanese patients with hepatocellular carcinoma |
title_full_unstemmed | Survival outcomes after stereotactic body radiotherapy for 79 Japanese patients with hepatocellular carcinoma |
title_short | Survival outcomes after stereotactic body radiotherapy for 79 Japanese patients with hepatocellular carcinoma |
title_sort | survival outcomes after stereotactic body radiotherapy for 79 japanese patients with hepatocellular carcinoma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426924/ https://www.ncbi.nlm.nih.gov/pubmed/25691453 http://dx.doi.org/10.1093/jrr/rru130 |
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