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Conventional fractionation should not be the standard of care for T2 glottic cancer

BACKGROUND: The aim of this study was to report outcomes and late toxicity following hypofractionated accelerated radiotherapy for T2 glottic cancers. We highlight the importance of hypofractionated treatments with shorter overall treatment times, in improving outcomes for T2 glottic cancers. We als...

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Autores principales: Dixon, Lynne M., Douglas, Catriona M., Shaukat, Shazril Imran, Garcez, Kate, Lee, Lip Wai, Sykes, Andrew J., Thomson, David, Slevin, Nicholas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686811/
https://www.ncbi.nlm.nih.gov/pubmed/29137654
http://dx.doi.org/10.1186/s13014-017-0915-8
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author Dixon, Lynne M.
Douglas, Catriona M.
Shaukat, Shazril Imran
Garcez, Kate
Lee, Lip Wai
Sykes, Andrew J.
Thomson, David
Slevin, Nicholas J.
author_facet Dixon, Lynne M.
Douglas, Catriona M.
Shaukat, Shazril Imran
Garcez, Kate
Lee, Lip Wai
Sykes, Andrew J.
Thomson, David
Slevin, Nicholas J.
author_sort Dixon, Lynne M.
collection PubMed
description BACKGROUND: The aim of this study was to report outcomes and late toxicity following hypofractionated accelerated radiotherapy for T2 glottic cancers. We highlight the importance of hypofractionated treatments with shorter overall treatment times, in improving outcomes for T2 glottic cancers. We also compare the biologically effective dose of hypofractionated regimes, with conventional fractionation. METHODS: One hundred twelve patients with T2 glottic cancer were treated between January 1999 and December 2005. All patients were prescribed a hypofractionated accelerated radiotherapy dose of 52.5 Gray in 3.28 Gray per fraction, delivered over 22 days. Radiobiological calculations were used to assess the relationship of fraction size and overall treatment time on local control outcomes and late toxicity. RESULTS: The 5-year overall survival was 67%, the 5-year local control was 82%, and the 5-year disease-specific survival was 90%. The respective 5-year local control for T2a and T2b disease was 88.8 and 70.8% (p = 0.032). Severe late toxicity occurred in two patients (1.8%). Radiobiological calculations showed an increase in local control of nearly 12%, with a 10 Gray increase in biologically effective dose. CONCLUSION: This study has demonstrated that accelerated hypofractionated regimes have improved local control and similar late toxicity compared with conventional fractionation schedules. This supports the use of hypofractionated regimes as the standard of care for early glottic laryngeal cancers.
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spelling pubmed-56868112017-11-21 Conventional fractionation should not be the standard of care for T2 glottic cancer Dixon, Lynne M. Douglas, Catriona M. Shaukat, Shazril Imran Garcez, Kate Lee, Lip Wai Sykes, Andrew J. Thomson, David Slevin, Nicholas J. Radiat Oncol Research BACKGROUND: The aim of this study was to report outcomes and late toxicity following hypofractionated accelerated radiotherapy for T2 glottic cancers. We highlight the importance of hypofractionated treatments with shorter overall treatment times, in improving outcomes for T2 glottic cancers. We also compare the biologically effective dose of hypofractionated regimes, with conventional fractionation. METHODS: One hundred twelve patients with T2 glottic cancer were treated between January 1999 and December 2005. All patients were prescribed a hypofractionated accelerated radiotherapy dose of 52.5 Gray in 3.28 Gray per fraction, delivered over 22 days. Radiobiological calculations were used to assess the relationship of fraction size and overall treatment time on local control outcomes and late toxicity. RESULTS: The 5-year overall survival was 67%, the 5-year local control was 82%, and the 5-year disease-specific survival was 90%. The respective 5-year local control for T2a and T2b disease was 88.8 and 70.8% (p = 0.032). Severe late toxicity occurred in two patients (1.8%). Radiobiological calculations showed an increase in local control of nearly 12%, with a 10 Gray increase in biologically effective dose. CONCLUSION: This study has demonstrated that accelerated hypofractionated regimes have improved local control and similar late toxicity compared with conventional fractionation schedules. This supports the use of hypofractionated regimes as the standard of care for early glottic laryngeal cancers. BioMed Central 2017-11-14 /pmc/articles/PMC5686811/ /pubmed/29137654 http://dx.doi.org/10.1186/s13014-017-0915-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Dixon, Lynne M.
Douglas, Catriona M.
Shaukat, Shazril Imran
Garcez, Kate
Lee, Lip Wai
Sykes, Andrew J.
Thomson, David
Slevin, Nicholas J.
Conventional fractionation should not be the standard of care for T2 glottic cancer
title Conventional fractionation should not be the standard of care for T2 glottic cancer
title_full Conventional fractionation should not be the standard of care for T2 glottic cancer
title_fullStr Conventional fractionation should not be the standard of care for T2 glottic cancer
title_full_unstemmed Conventional fractionation should not be the standard of care for T2 glottic cancer
title_short Conventional fractionation should not be the standard of care for T2 glottic cancer
title_sort conventional fractionation should not be the standard of care for t2 glottic cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686811/
https://www.ncbi.nlm.nih.gov/pubmed/29137654
http://dx.doi.org/10.1186/s13014-017-0915-8
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