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Clinical outcomes and dosimetric study of hypofractionated Helical TomoTherapy in breast cancer patients

We present a single center’s experience of treatment outcomes and dosimetric parameters for breast cancer patients treated with hypofractionated Helical TomoTherapy (HT). This is a retrospective study of one hundred and thirty-six patients with invasive breast cancer treated between March 2012 and O...

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Autores principales: Chitapanarux, Imjai, Nobnop, Wannapha, Tippanya, Damrongsak, Sripan, Patumrat, Chakrabandhu, Somvilai, Klunklin, Pitchayaponne, Onchan, Wimrak, Jia-Mahasap, Bongkot, Tharavichitkul, Ekkasit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355009/
https://www.ncbi.nlm.nih.gov/pubmed/30703145
http://dx.doi.org/10.1371/journal.pone.0211578
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author Chitapanarux, Imjai
Nobnop, Wannapha
Tippanya, Damrongsak
Sripan, Patumrat
Chakrabandhu, Somvilai
Klunklin, Pitchayaponne
Onchan, Wimrak
Jia-Mahasap, Bongkot
Tharavichitkul, Ekkasit
author_facet Chitapanarux, Imjai
Nobnop, Wannapha
Tippanya, Damrongsak
Sripan, Patumrat
Chakrabandhu, Somvilai
Klunklin, Pitchayaponne
Onchan, Wimrak
Jia-Mahasap, Bongkot
Tharavichitkul, Ekkasit
author_sort Chitapanarux, Imjai
collection PubMed
description We present a single center’s experience of treatment outcomes and dosimetric parameters for breast cancer patients treated with hypofractionated Helical TomoTherapy (HT). This is a retrospective study of one hundred and thirty-six patients with invasive breast cancer treated between March 2012 and October 2016. Dosimetric parameters and 3-year loco-regional failure free survival (LRFFS) were analyzed. Dose to ipsilateral lung, heart and contralateral breast as well as acute and late toxicities were recorded. The median follow-up time is 45 months (range: 5–83). Two patients had loco-regional failure. The 3-year LRFFS was 99%. Acute grade 1 and 2 skin toxicities occurred in 95% and 1%, respectively. Coverage of the target volumes was achieved with the mean ± standard deviation (SD) of homogeneity and conformity index being 0.1 ± 0.04, and 0.8 ± 0.07, respectively. Dose to ipsilateral lung, contralateral breast, and heart was also within the limited constraints regardless of the complexity of target volumes. Only two percent of patients experienced late grade 2 skin toxicity. No late grade 2 subcutaneous tissue toxicity was found. Nine percent of patients developed late grade 1 lung toxicity. Hypofractionated radiotherapy using Helical TomoTherapy in breast irradiation provides excellent 3-year LRFFS and minimal acute and late toxicities. A careful, longer follow-up of healthy tissue effects to lung, heart, and contralateral breast is warranted.
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spelling pubmed-63550092019-02-15 Clinical outcomes and dosimetric study of hypofractionated Helical TomoTherapy in breast cancer patients Chitapanarux, Imjai Nobnop, Wannapha Tippanya, Damrongsak Sripan, Patumrat Chakrabandhu, Somvilai Klunklin, Pitchayaponne Onchan, Wimrak Jia-Mahasap, Bongkot Tharavichitkul, Ekkasit PLoS One Research Article We present a single center’s experience of treatment outcomes and dosimetric parameters for breast cancer patients treated with hypofractionated Helical TomoTherapy (HT). This is a retrospective study of one hundred and thirty-six patients with invasive breast cancer treated between March 2012 and October 2016. Dosimetric parameters and 3-year loco-regional failure free survival (LRFFS) were analyzed. Dose to ipsilateral lung, heart and contralateral breast as well as acute and late toxicities were recorded. The median follow-up time is 45 months (range: 5–83). Two patients had loco-regional failure. The 3-year LRFFS was 99%. Acute grade 1 and 2 skin toxicities occurred in 95% and 1%, respectively. Coverage of the target volumes was achieved with the mean ± standard deviation (SD) of homogeneity and conformity index being 0.1 ± 0.04, and 0.8 ± 0.07, respectively. Dose to ipsilateral lung, contralateral breast, and heart was also within the limited constraints regardless of the complexity of target volumes. Only two percent of patients experienced late grade 2 skin toxicity. No late grade 2 subcutaneous tissue toxicity was found. Nine percent of patients developed late grade 1 lung toxicity. Hypofractionated radiotherapy using Helical TomoTherapy in breast irradiation provides excellent 3-year LRFFS and minimal acute and late toxicities. A careful, longer follow-up of healthy tissue effects to lung, heart, and contralateral breast is warranted. Public Library of Science 2019-01-31 /pmc/articles/PMC6355009/ /pubmed/30703145 http://dx.doi.org/10.1371/journal.pone.0211578 Text en © 2019 Chitapanarux et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chitapanarux, Imjai
Nobnop, Wannapha
Tippanya, Damrongsak
Sripan, Patumrat
Chakrabandhu, Somvilai
Klunklin, Pitchayaponne
Onchan, Wimrak
Jia-Mahasap, Bongkot
Tharavichitkul, Ekkasit
Clinical outcomes and dosimetric study of hypofractionated Helical TomoTherapy in breast cancer patients
title Clinical outcomes and dosimetric study of hypofractionated Helical TomoTherapy in breast cancer patients
title_full Clinical outcomes and dosimetric study of hypofractionated Helical TomoTherapy in breast cancer patients
title_fullStr Clinical outcomes and dosimetric study of hypofractionated Helical TomoTherapy in breast cancer patients
title_full_unstemmed Clinical outcomes and dosimetric study of hypofractionated Helical TomoTherapy in breast cancer patients
title_short Clinical outcomes and dosimetric study of hypofractionated Helical TomoTherapy in breast cancer patients
title_sort clinical outcomes and dosimetric study of hypofractionated helical tomotherapy in breast cancer patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355009/
https://www.ncbi.nlm.nih.gov/pubmed/30703145
http://dx.doi.org/10.1371/journal.pone.0211578
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