Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mohamad, Osama, Imai, Reiko, Kamada, Tadashi, Nitta, Yuki, Araki, Nobuhito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
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
_version_ 1783323707991654400
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
work_keys_str_mv AT mohamadosama carbonionradiotherapyforinoperablepediatricosteosarcoma
AT imaireiko carbonionradiotherapyforinoperablepediatricosteosarcoma
AT kamadatadashi carbonionradiotherapyforinoperablepediatricosteosarcoma
AT nittayuki carbonionradiotherapyforinoperablepediatricosteosarcoma
AT arakinobuhito carbonionradiotherapyforinoperablepediatricosteosarcoma
AT carbonionradiotherapyforinoperablepediatricosteosarcoma