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Radiation therapy combined with bone-modifying agents ameliorates local control of osteolytic bone metastases in breast cancer

Bone-modifying agents (BMAs) are frequently used for the treatment of bone metastases. Both BMA and radiation therapy (RT) are effective; however, there are few studies that have evaluated the efficacy of the combination treatment. We evaluated the effectiveness of RT + BMA in breast cancer-induced...

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Autores principales: Tanaka, Hidekazu, Makita, Chiyoko, Manabe, Yuki, Kajima, Miki, Matsuyama, Katsuya, Matsuo, Masayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299266/
https://www.ncbi.nlm.nih.gov/pubmed/32266394
http://dx.doi.org/10.1093/jrr/rraa020
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author Tanaka, Hidekazu
Makita, Chiyoko
Manabe, Yuki
Kajima, Miki
Matsuyama, Katsuya
Matsuo, Masayuki
author_facet Tanaka, Hidekazu
Makita, Chiyoko
Manabe, Yuki
Kajima, Miki
Matsuyama, Katsuya
Matsuo, Masayuki
author_sort Tanaka, Hidekazu
collection PubMed
description Bone-modifying agents (BMAs) are frequently used for the treatment of bone metastases. Both BMA and radiation therapy (RT) are effective; however, there are few studies that have evaluated the efficacy of the combination treatment. We evaluated the effectiveness of RT + BMA in breast cancer-induced osteolytic bone metastasis as compared to BMA alone. A total of 43 lesions in 25 patients were evaluated. The median follow-up period was 18 (range, 2–90) months. None of the lesions was treated with chemotherapy or molecular targeted drugs during the follow-up period for evaluating the local response. Patients with complete or partial response were considered as responders, while those with stable or progressive disease were considered as non-responders. The rate of response with RT + BMA was significantly higher than that with BMA alone (P = 0.001). The cumulative incidence rate of response at 6 months was 54.4% in the RT + BMA group and 27.5% in the BMA alone group. The median time to response was 4 (range, 2–11) months in the RT + BMA group and 6 (range, 4–16) months in the BMA alone group. The overall survival rate in the responder group (83.1% at 1 year) was significantly higher than that in the non-responder group (37.5% at 1 year) (P = 0.029). In conclusion, RT combined with BMA was found to be more effective than BMA alone for the treatment of osteolytic bone metastasis, which thereby improves the prognosis.
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spelling pubmed-72992662020-06-23 Radiation therapy combined with bone-modifying agents ameliorates local control of osteolytic bone metastases in breast cancer Tanaka, Hidekazu Makita, Chiyoko Manabe, Yuki Kajima, Miki Matsuyama, Katsuya Matsuo, Masayuki J Radiat Res Regular Paper Bone-modifying agents (BMAs) are frequently used for the treatment of bone metastases. Both BMA and radiation therapy (RT) are effective; however, there are few studies that have evaluated the efficacy of the combination treatment. We evaluated the effectiveness of RT + BMA in breast cancer-induced osteolytic bone metastasis as compared to BMA alone. A total of 43 lesions in 25 patients were evaluated. The median follow-up period was 18 (range, 2–90) months. None of the lesions was treated with chemotherapy or molecular targeted drugs during the follow-up period for evaluating the local response. Patients with complete or partial response were considered as responders, while those with stable or progressive disease were considered as non-responders. The rate of response with RT + BMA was significantly higher than that with BMA alone (P = 0.001). The cumulative incidence rate of response at 6 months was 54.4% in the RT + BMA group and 27.5% in the BMA alone group. The median time to response was 4 (range, 2–11) months in the RT + BMA group and 6 (range, 4–16) months in the BMA alone group. The overall survival rate in the responder group (83.1% at 1 year) was significantly higher than that in the non-responder group (37.5% at 1 year) (P = 0.029). In conclusion, RT combined with BMA was found to be more effective than BMA alone for the treatment of osteolytic bone metastasis, which thereby improves the prognosis. Oxford University Press 2020-04-08 /pmc/articles/PMC7299266/ /pubmed/32266394 http://dx.doi.org/10.1093/jrr/rraa020 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of The Japanese Radiation Research Society and Japanese Society for Radiation Oncology. All rights reserved. For Permissions, please email: journals.permissions@oup.com 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 non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Regular Paper
Tanaka, Hidekazu
Makita, Chiyoko
Manabe, Yuki
Kajima, Miki
Matsuyama, Katsuya
Matsuo, Masayuki
Radiation therapy combined with bone-modifying agents ameliorates local control of osteolytic bone metastases in breast cancer
title Radiation therapy combined with bone-modifying agents ameliorates local control of osteolytic bone metastases in breast cancer
title_full Radiation therapy combined with bone-modifying agents ameliorates local control of osteolytic bone metastases in breast cancer
title_fullStr Radiation therapy combined with bone-modifying agents ameliorates local control of osteolytic bone metastases in breast cancer
title_full_unstemmed Radiation therapy combined with bone-modifying agents ameliorates local control of osteolytic bone metastases in breast cancer
title_short Radiation therapy combined with bone-modifying agents ameliorates local control of osteolytic bone metastases in breast cancer
title_sort radiation therapy combined with bone-modifying agents ameliorates local control of osteolytic bone metastases in breast cancer
topic Regular Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299266/
https://www.ncbi.nlm.nih.gov/pubmed/32266394
http://dx.doi.org/10.1093/jrr/rraa020
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