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Hypofractionated radiotherapy after conservative surgery for breast cancer: analysis of acute and late toxicity

BACKGROUND: A variety of hypofractionated radiotherapy schedules has been proposed after breast conserving surgery in the attempt to shorten the overall treatment time. The aim of the present study is to assess acute and late toxicity of using daily fractionation of 2.25 Gy to a total dose of 45 Gy...

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Autores principales: Deantonio, Letizia, Gambaro, Giuseppina, Beldì, Debora, Masini, Laura, Tunesi, Sara, Magnani, Corrado, Krengli, Marco
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000406/
https://www.ncbi.nlm.nih.gov/pubmed/21092288
http://dx.doi.org/10.1186/1748-717X-5-112
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author Deantonio, Letizia
Gambaro, Giuseppina
Beldì, Debora
Masini, Laura
Tunesi, Sara
Magnani, Corrado
Krengli, Marco
author_facet Deantonio, Letizia
Gambaro, Giuseppina
Beldì, Debora
Masini, Laura
Tunesi, Sara
Magnani, Corrado
Krengli, Marco
author_sort Deantonio, Letizia
collection PubMed
description BACKGROUND: A variety of hypofractionated radiotherapy schedules has been proposed after breast conserving surgery in the attempt to shorten the overall treatment time. The aim of the present study is to assess acute and late toxicity of using daily fractionation of 2.25 Gy to a total dose of 45 Gy to the whole breast in a mono-institutional series. METHODS: Eighty-five women with early breast cancer were assigned to receive 45 Gy followed by a boost to the tumour bed. Early and late toxicity were scored according to the Radiation Therapy Oncology Group criteria. For comparison, a group of 70 patients with similar characteristics and treated with conventional fractionation of 2 Gy to a total dose of 50 Gy in 25 fractions followed by a boost, was retrospectively selected. RESULTS: Overall median treatment duration was 29 days for hypofractionated radiotherapy and 37 days for conventional radiotherapy. Early reactions were observed in 72/85 (85%) patients treated with hypofractionation and in 67/70 (96%) patients treated with conventional fractionation (p = 0.01). Late toxicity was observed in 8 patients (10%) in the hypofractionation group and in 10 patients (15%) in the conventional fractionation group, respectively (p = 0.4). CONCLUSIONS: The hypofractionated schedule delivering 45 Gy in 20 fractions shortened the overall treatment time by 1 week with a reduction of skin acute toxicity and no increase of late effects compared to the conventional fractionation. Our results support the implementation of hypofractionated schedules in clinical practice.
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spelling pubmed-30004062010-12-10 Hypofractionated radiotherapy after conservative surgery for breast cancer: analysis of acute and late toxicity Deantonio, Letizia Gambaro, Giuseppina Beldì, Debora Masini, Laura Tunesi, Sara Magnani, Corrado Krengli, Marco Radiat Oncol Research BACKGROUND: A variety of hypofractionated radiotherapy schedules has been proposed after breast conserving surgery in the attempt to shorten the overall treatment time. The aim of the present study is to assess acute and late toxicity of using daily fractionation of 2.25 Gy to a total dose of 45 Gy to the whole breast in a mono-institutional series. METHODS: Eighty-five women with early breast cancer were assigned to receive 45 Gy followed by a boost to the tumour bed. Early and late toxicity were scored according to the Radiation Therapy Oncology Group criteria. For comparison, a group of 70 patients with similar characteristics and treated with conventional fractionation of 2 Gy to a total dose of 50 Gy in 25 fractions followed by a boost, was retrospectively selected. RESULTS: Overall median treatment duration was 29 days for hypofractionated radiotherapy and 37 days for conventional radiotherapy. Early reactions were observed in 72/85 (85%) patients treated with hypofractionation and in 67/70 (96%) patients treated with conventional fractionation (p = 0.01). Late toxicity was observed in 8 patients (10%) in the hypofractionation group and in 10 patients (15%) in the conventional fractionation group, respectively (p = 0.4). CONCLUSIONS: The hypofractionated schedule delivering 45 Gy in 20 fractions shortened the overall treatment time by 1 week with a reduction of skin acute toxicity and no increase of late effects compared to the conventional fractionation. Our results support the implementation of hypofractionated schedules in clinical practice. BioMed Central 2010-11-23 /pmc/articles/PMC3000406/ /pubmed/21092288 http://dx.doi.org/10.1186/1748-717X-5-112 Text en Copyright ©2010 Deantonio et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Deantonio, Letizia
Gambaro, Giuseppina
Beldì, Debora
Masini, Laura
Tunesi, Sara
Magnani, Corrado
Krengli, Marco
Hypofractionated radiotherapy after conservative surgery for breast cancer: analysis of acute and late toxicity
title Hypofractionated radiotherapy after conservative surgery for breast cancer: analysis of acute and late toxicity
title_full Hypofractionated radiotherapy after conservative surgery for breast cancer: analysis of acute and late toxicity
title_fullStr Hypofractionated radiotherapy after conservative surgery for breast cancer: analysis of acute and late toxicity
title_full_unstemmed Hypofractionated radiotherapy after conservative surgery for breast cancer: analysis of acute and late toxicity
title_short Hypofractionated radiotherapy after conservative surgery for breast cancer: analysis of acute and late toxicity
title_sort hypofractionated radiotherapy after conservative surgery for breast cancer: analysis of acute and late toxicity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000406/
https://www.ncbi.nlm.nih.gov/pubmed/21092288
http://dx.doi.org/10.1186/1748-717X-5-112
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