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IMRT sparing of normal tissues in locoregional treatment of breast cancer

PURPOSE: This clinical study was designed to prospectively evaluate the acute and moderately-late cardiac and lung toxicities of intensity modulated radiation therapy delivered by helical tomotherapy (IMRT-HT) for locoregional breast radiation treatment including the internal mammary nodes (IMN). MA...

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Autores principales: Caudrelier, Jean-Michel, Meng, Joanne, Esche, Bernd, Grimard, Laval, Ruddy, Terrence, Amjadi, Kayvan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223821/
https://www.ncbi.nlm.nih.gov/pubmed/25052720
http://dx.doi.org/10.1186/1748-717X-9-161
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author Caudrelier, Jean-Michel
Meng, Joanne
Esche, Bernd
Grimard, Laval
Ruddy, Terrence
Amjadi, Kayvan
author_facet Caudrelier, Jean-Michel
Meng, Joanne
Esche, Bernd
Grimard, Laval
Ruddy, Terrence
Amjadi, Kayvan
author_sort Caudrelier, Jean-Michel
collection PubMed
description PURPOSE: This clinical study was designed to prospectively evaluate the acute and moderately-late cardiac and lung toxicities of intensity modulated radiation therapy delivered by helical tomotherapy (IMRT-HT) for locoregional breast radiation treatment including the internal mammary nodes (IMN). MATERIAL/METHODS: 30 patients with stage III breast cancers have been accrued in this study. All patients received adjuvant chemotherapy. Target volumes were defined as follows: the PTV included breast/chest wall, axillary level II, III, infra/supraclavicular, IM nodes CTVs plus 3 mm margins. The heart with subunits and the lungs were defined as critical organs. Dose to PTV was 50 Gy in 25 fractions. Acute toxicities were assessed every week and 2 weeks post treatment using the CTCAE v3.0.scale. The moderately-late toxicities were assessed clinically plus by cardiac myoview perfusion tests scheduled at baseline, 3 and 12-month follow-up, as well a CT chest at the 6 month follow-up. The data analysis is descriptive. RESULTS: All participants completed the 5-week course of radiation without interruption. Skin erythema was modest and mainly grade 1–2 between the 3rd and the 5th week of radiation treatment. Only 4/30 patients experienced grade 3 skin reactions, mostly seen 2 weeks post radiation. Only 5 patients demonstrated grade 1 or 2 dyspnea, but 3 of them already had symptoms pre-radiation treatment. With a median follow-up of 58 (24–76) months, there have been infrequent moderately-late side effects. Most were grade 1 and were sometimes present at the baseline assessment. Cardiac myoview tests done at baseline and 1-year follow-up for 15 out of 18 left sided breast cancers did not show any abnormalities related to radiation. The 6-month follow-up chest CT-scans done for 25 out of 30 patients showed minimal anterior lung fibrosis for 7 patients and were completely normal for the other 18. No locoregional recurrence has been recorded and the 5-year survival is 78% (95% CI: 70-97%). CONCLUSION: IMRT-HT for locoregional breast radiation is very well tolerated with minimal acute or moderately-late side effects. Cardiac and respiratory tests did not show any strong evidence of significant treatment related abnormalities. TRIAL REGISTRATION: clinicaltrials.gov: http://NCT00508352.
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spelling pubmed-42238212014-11-08 IMRT sparing of normal tissues in locoregional treatment of breast cancer Caudrelier, Jean-Michel Meng, Joanne Esche, Bernd Grimard, Laval Ruddy, Terrence Amjadi, Kayvan Radiat Oncol Research PURPOSE: This clinical study was designed to prospectively evaluate the acute and moderately-late cardiac and lung toxicities of intensity modulated radiation therapy delivered by helical tomotherapy (IMRT-HT) for locoregional breast radiation treatment including the internal mammary nodes (IMN). MATERIAL/METHODS: 30 patients with stage III breast cancers have been accrued in this study. All patients received adjuvant chemotherapy. Target volumes were defined as follows: the PTV included breast/chest wall, axillary level II, III, infra/supraclavicular, IM nodes CTVs plus 3 mm margins. The heart with subunits and the lungs were defined as critical organs. Dose to PTV was 50 Gy in 25 fractions. Acute toxicities were assessed every week and 2 weeks post treatment using the CTCAE v3.0.scale. The moderately-late toxicities were assessed clinically plus by cardiac myoview perfusion tests scheduled at baseline, 3 and 12-month follow-up, as well a CT chest at the 6 month follow-up. The data analysis is descriptive. RESULTS: All participants completed the 5-week course of radiation without interruption. Skin erythema was modest and mainly grade 1–2 between the 3rd and the 5th week of radiation treatment. Only 4/30 patients experienced grade 3 skin reactions, mostly seen 2 weeks post radiation. Only 5 patients demonstrated grade 1 or 2 dyspnea, but 3 of them already had symptoms pre-radiation treatment. With a median follow-up of 58 (24–76) months, there have been infrequent moderately-late side effects. Most were grade 1 and were sometimes present at the baseline assessment. Cardiac myoview tests done at baseline and 1-year follow-up for 15 out of 18 left sided breast cancers did not show any abnormalities related to radiation. The 6-month follow-up chest CT-scans done for 25 out of 30 patients showed minimal anterior lung fibrosis for 7 patients and were completely normal for the other 18. No locoregional recurrence has been recorded and the 5-year survival is 78% (95% CI: 70-97%). CONCLUSION: IMRT-HT for locoregional breast radiation is very well tolerated with minimal acute or moderately-late side effects. Cardiac and respiratory tests did not show any strong evidence of significant treatment related abnormalities. TRIAL REGISTRATION: clinicaltrials.gov: http://NCT00508352. BioMed Central 2014-07-22 /pmc/articles/PMC4223821/ /pubmed/25052720 http://dx.doi.org/10.1186/1748-717X-9-161 Text en Copyright © 2014 Caudrelier 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 credited. 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
Caudrelier, Jean-Michel
Meng, Joanne
Esche, Bernd
Grimard, Laval
Ruddy, Terrence
Amjadi, Kayvan
IMRT sparing of normal tissues in locoregional treatment of breast cancer
title IMRT sparing of normal tissues in locoregional treatment of breast cancer
title_full IMRT sparing of normal tissues in locoregional treatment of breast cancer
title_fullStr IMRT sparing of normal tissues in locoregional treatment of breast cancer
title_full_unstemmed IMRT sparing of normal tissues in locoregional treatment of breast cancer
title_short IMRT sparing of normal tissues in locoregional treatment of breast cancer
title_sort imrt sparing of normal tissues in locoregional treatment of breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223821/
https://www.ncbi.nlm.nih.gov/pubmed/25052720
http://dx.doi.org/10.1186/1748-717X-9-161
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