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High-dose pre-operative helical tomotherapy (54 Gy) for retroperitoneal liposarcoma

PURPOSE: To evaluate the feasibility of pre-operative radiotherapy (54 Gy) with Helical Tomotherapy (HT) followed by surgery. METHODS AND MATERIALS: Ten patients with non-metastatic resectable retroperitoneal liposarcomas were treated by pre-operative tomotherapy (54 Gy) and surgery. Clinical and bi...

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Autores principales: Sargos, Paul, Dejean, Catherine, Figueiredo, Bénédicte Henriques de, Brouste, Véronique, Nguyen Bui, Binh, Italiano, Antoine, Stoeckle, Eberhard, Kantor, Guy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551784/
https://www.ncbi.nlm.nih.gov/pubmed/23245199
http://dx.doi.org/10.1186/1748-717X-7-214
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author Sargos, Paul
Dejean, Catherine
Figueiredo, Bénédicte Henriques de
Brouste, Véronique
Nguyen Bui, Binh
Italiano, Antoine
Stoeckle, Eberhard
Kantor, Guy
author_facet Sargos, Paul
Dejean, Catherine
Figueiredo, Bénédicte Henriques de
Brouste, Véronique
Nguyen Bui, Binh
Italiano, Antoine
Stoeckle, Eberhard
Kantor, Guy
author_sort Sargos, Paul
collection PubMed
description PURPOSE: To evaluate the feasibility of pre-operative radiotherapy (54 Gy) with Helical Tomotherapy (HT) followed by surgery. METHODS AND MATERIALS: Ten patients with non-metastatic resectable retroperitoneal liposarcomas were treated by pre-operative tomotherapy (54 Gy) and surgery. Clinical and biological toxicities were evaluated on the CTCAEV3.0 scale. For nine patients, delivered tomotherapy plans were compared with retrospectively-planned dynamic intensity-modulated radiotherapy (IMRT) dosimetric studies. RESULTS: No immediate or late Grade>2 toxicities were observed after radiotherapy. Post-operatively, one patient died and three patients experienced Grade 3 toxicity (two digestive and one metabolic). These toxicities disappeared and only two patients presented persistent Grade 1 paresthesia. R0 resection was obtained for four patients, R1 for four, and R2 resection for two. With a median follow-up of 26 months, no local or metastatic relapse was observed. Dosimetric comparisons between HT and retrospectively-planned IMRT demonstrate adequate target volume coverage for both techniques. Gastrointestinal sparing is higher with HT with a D200cc reduced by 5 Gy. Integral dose (ID) was increased in HT. CONCLUSIONS: High dose pre-operative radiotherapy (54 Gy) for retroperitoneal liposarcoma is feasible and mostly well tolerated. Cumulative toxicity and tolerance depend mainly on patient’s general status. Image-guided radiation therapy (IGRT) is essential, irrespective of the IMRT technique used. Furthermore, HT offers the possibility of sparing selected areas in such complex volumes.
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spelling pubmed-35517842013-01-24 High-dose pre-operative helical tomotherapy (54 Gy) for retroperitoneal liposarcoma Sargos, Paul Dejean, Catherine Figueiredo, Bénédicte Henriques de Brouste, Véronique Nguyen Bui, Binh Italiano, Antoine Stoeckle, Eberhard Kantor, Guy Radiat Oncol Research PURPOSE: To evaluate the feasibility of pre-operative radiotherapy (54 Gy) with Helical Tomotherapy (HT) followed by surgery. METHODS AND MATERIALS: Ten patients with non-metastatic resectable retroperitoneal liposarcomas were treated by pre-operative tomotherapy (54 Gy) and surgery. Clinical and biological toxicities were evaluated on the CTCAEV3.0 scale. For nine patients, delivered tomotherapy plans were compared with retrospectively-planned dynamic intensity-modulated radiotherapy (IMRT) dosimetric studies. RESULTS: No immediate or late Grade>2 toxicities were observed after radiotherapy. Post-operatively, one patient died and three patients experienced Grade 3 toxicity (two digestive and one metabolic). These toxicities disappeared and only two patients presented persistent Grade 1 paresthesia. R0 resection was obtained for four patients, R1 for four, and R2 resection for two. With a median follow-up of 26 months, no local or metastatic relapse was observed. Dosimetric comparisons between HT and retrospectively-planned IMRT demonstrate adequate target volume coverage for both techniques. Gastrointestinal sparing is higher with HT with a D200cc reduced by 5 Gy. Integral dose (ID) was increased in HT. CONCLUSIONS: High dose pre-operative radiotherapy (54 Gy) for retroperitoneal liposarcoma is feasible and mostly well tolerated. Cumulative toxicity and tolerance depend mainly on patient’s general status. Image-guided radiation therapy (IGRT) is essential, irrespective of the IMRT technique used. Furthermore, HT offers the possibility of sparing selected areas in such complex volumes. BioMed Central 2012-12-17 /pmc/articles/PMC3551784/ /pubmed/23245199 http://dx.doi.org/10.1186/1748-717X-7-214 Text en Copyright ©2012 Sargos 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
Sargos, Paul
Dejean, Catherine
Figueiredo, Bénédicte Henriques de
Brouste, Véronique
Nguyen Bui, Binh
Italiano, Antoine
Stoeckle, Eberhard
Kantor, Guy
High-dose pre-operative helical tomotherapy (54 Gy) for retroperitoneal liposarcoma
title High-dose pre-operative helical tomotherapy (54 Gy) for retroperitoneal liposarcoma
title_full High-dose pre-operative helical tomotherapy (54 Gy) for retroperitoneal liposarcoma
title_fullStr High-dose pre-operative helical tomotherapy (54 Gy) for retroperitoneal liposarcoma
title_full_unstemmed High-dose pre-operative helical tomotherapy (54 Gy) for retroperitoneal liposarcoma
title_short High-dose pre-operative helical tomotherapy (54 Gy) for retroperitoneal liposarcoma
title_sort high-dose pre-operative helical tomotherapy (54 gy) for retroperitoneal liposarcoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551784/
https://www.ncbi.nlm.nih.gov/pubmed/23245199
http://dx.doi.org/10.1186/1748-717X-7-214
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