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Carbon ion radiotherapy for inoperable pediatric osteosarcoma
BACKGROUND: Unresectable pediatric osteosarcoma has poor outcomes with conventional treatments. RESULTS: Twenty-six patients aged 11–20 years (median 16) had inoperable osteosarcoma of the trunk (24 pelvic, 1 mediastinal and 1 paravertebral) without any other lesion at initial examination. There wer...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955418/ https://www.ncbi.nlm.nih.gov/pubmed/29796166 http://dx.doi.org/10.18632/oncotarget.25165 |
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author | Mohamad, Osama Imai, Reiko Kamada, Tadashi Nitta, Yuki Araki, Nobuhito |
author_facet | Mohamad, Osama Imai, Reiko Kamada, Tadashi Nitta, Yuki Araki, Nobuhito |
author_sort | Mohamad, Osama |
collection | PubMed |
description | BACKGROUND: Unresectable pediatric osteosarcoma has poor outcomes with conventional treatments. RESULTS: Twenty-six patients aged 11–20 years (median 16) had inoperable osteosarcoma of the trunk (24 pelvic, 1 mediastinal and 1 paravertebral) without any other lesion at initial examination. There were 22 primary, 1 locally recurrent and 3 metastatic cases. Median CIRT dose was 70.4 Gy RBE (relative biological effectiveness) delivered in 16 fractions. Median follow-up was 32.7 months. Overall survival was 50.0% and 41.7% at 3 and 5 years, respectively. Ten patients survived for more than 5 years (range 5–20.7 years). Local control was 69.9% and 62.9% at 3 and 5 years, respectively and progression-free survival was 34.6% at 3 and 5 years. Only largest tumor diameter correlated with 5-year overall survival and local control. There were 4 grade 3-4 CIRT-related late toxicities, 1 case of bone fracture and no treatment-related mortalities. All patients (except 1) were able to ambulate after CIRT. CONCLUSIONS: CIRT was safe and efficacious in the treatment of inoperable pediatric osteosarcoma with improved local control and overall survival compared to conventional treatments. METHODS: We retrospectively reviewed the records of pediatric and adolescent patients who received carbon ion radiotherapy (CIRT) for inoperable osteosarcoma between 1996 and 2014. |
format | Online Article Text |
id | pubmed-5955418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-59554182018-05-24 Carbon ion radiotherapy for inoperable pediatric osteosarcoma Mohamad, Osama Imai, Reiko Kamada, Tadashi Nitta, Yuki Araki, Nobuhito Oncotarget Research Paper BACKGROUND: Unresectable pediatric osteosarcoma has poor outcomes with conventional treatments. RESULTS: Twenty-six patients aged 11–20 years (median 16) had inoperable osteosarcoma of the trunk (24 pelvic, 1 mediastinal and 1 paravertebral) without any other lesion at initial examination. There were 22 primary, 1 locally recurrent and 3 metastatic cases. Median CIRT dose was 70.4 Gy RBE (relative biological effectiveness) delivered in 16 fractions. Median follow-up was 32.7 months. Overall survival was 50.0% and 41.7% at 3 and 5 years, respectively. Ten patients survived for more than 5 years (range 5–20.7 years). Local control was 69.9% and 62.9% at 3 and 5 years, respectively and progression-free survival was 34.6% at 3 and 5 years. Only largest tumor diameter correlated with 5-year overall survival and local control. There were 4 grade 3-4 CIRT-related late toxicities, 1 case of bone fracture and no treatment-related mortalities. All patients (except 1) were able to ambulate after CIRT. CONCLUSIONS: CIRT was safe and efficacious in the treatment of inoperable pediatric osteosarcoma with improved local control and overall survival compared to conventional treatments. METHODS: We retrospectively reviewed the records of pediatric and adolescent patients who received carbon ion radiotherapy (CIRT) for inoperable osteosarcoma between 1996 and 2014. Impact Journals LLC 2018-05-01 /pmc/articles/PMC5955418/ /pubmed/29796166 http://dx.doi.org/10.18632/oncotarget.25165 Text en Copyright: © 2018 Mohamad 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 (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Mohamad, Osama Imai, Reiko Kamada, Tadashi Nitta, Yuki Araki, Nobuhito Carbon ion radiotherapy for inoperable pediatric osteosarcoma |
title | Carbon ion radiotherapy for inoperable pediatric osteosarcoma |
title_full | Carbon ion radiotherapy for inoperable pediatric osteosarcoma |
title_fullStr | Carbon ion radiotherapy for inoperable pediatric osteosarcoma |
title_full_unstemmed | Carbon ion radiotherapy for inoperable pediatric osteosarcoma |
title_short | Carbon ion radiotherapy for inoperable pediatric osteosarcoma |
title_sort | carbon ion radiotherapy for inoperable pediatric osteosarcoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955418/ https://www.ncbi.nlm.nih.gov/pubmed/29796166 http://dx.doi.org/10.18632/oncotarget.25165 |
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