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Optimal radiotherapy strategy for primary or recurrent fibromatosis and long-term results

PURPOSE: Although locally invasive or recurrent fibromatosis is primarily treated with surgery, radiotherapy (RT) produces local control for recurrent/unresectable tumors or those with positive surgical margins. Herein, we describe our updated institutional experience with RT to treat fibromatosis....

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Autores principales: Choi, Seo Hee, Yoon, Hong In, Kim, Seung Hyun, Kim, Sang Kyum, Shin, Kyoo-Ho, Suh, Chang-Ok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973595/
https://www.ncbi.nlm.nih.gov/pubmed/29813130
http://dx.doi.org/10.1371/journal.pone.0198134
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author Choi, Seo Hee
Yoon, Hong In
Kim, Seung Hyun
Kim, Sang Kyum
Shin, Kyoo-Ho
Suh, Chang-Ok
author_facet Choi, Seo Hee
Yoon, Hong In
Kim, Seung Hyun
Kim, Sang Kyum
Shin, Kyoo-Ho
Suh, Chang-Ok
author_sort Choi, Seo Hee
collection PubMed
description PURPOSE: Although locally invasive or recurrent fibromatosis is primarily treated with surgery, radiotherapy (RT) produces local control for recurrent/unresectable tumors or those with positive surgical margins. Herein, we describe our updated institutional experience with RT to treat fibromatosis. METHODS: Forty-seven patients with fibromatosis received RT between 1990 and 2015, and were followed for ≥12 months. Eight patients received RT for gross tumors, and 39 received postoperative RT after single/multiple prior surgeries. A median dose of 54 Gy was prescribed for definitive RT; 48.6, 50.4, and 54 Gy were prescribed for R0, R1, and R2 resected tumors, respectively. Recurrences were classified as in-field, marginal, or out-field. Prognostic factors were also evaluated. RESULTS: Seven recurrences were noted, including 2 in-field, 4 marginal, and 1 out-field, after a median follow-up of 60 months. In-field recurrences occurred in 1 patient who received 40.5 Gy of salvage RT after postoperative recurrence and another who received 45 Gy for R1 resection after multiple prior operations. All marginal failures were due to insufficient clinical target volume (CTV) margins regardless of dose (3 with 45 Gy and 1 with 54 Gy). On multivariate analysis, a CTV margin ≥5 cm and dose >45 Gy were significant predictors of non-recurrence (p = 0.039 and 0.049, respectively). Subgroup analysis showed that patients with both an CTV margin ≥5 cm and a dose >45 Gy showed a favorable outcome. CONCLUSIONS: RT is a valuable option for treating aggressive fibromatosis; doses ≥45 Gy and a large field produce optimal results. For in-field control, a higher dose is more necessary for gross residual tumors than for totally excised lesions.
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spelling pubmed-59735952018-06-08 Optimal radiotherapy strategy for primary or recurrent fibromatosis and long-term results Choi, Seo Hee Yoon, Hong In Kim, Seung Hyun Kim, Sang Kyum Shin, Kyoo-Ho Suh, Chang-Ok PLoS One Research Article PURPOSE: Although locally invasive or recurrent fibromatosis is primarily treated with surgery, radiotherapy (RT) produces local control for recurrent/unresectable tumors or those with positive surgical margins. Herein, we describe our updated institutional experience with RT to treat fibromatosis. METHODS: Forty-seven patients with fibromatosis received RT between 1990 and 2015, and were followed for ≥12 months. Eight patients received RT for gross tumors, and 39 received postoperative RT after single/multiple prior surgeries. A median dose of 54 Gy was prescribed for definitive RT; 48.6, 50.4, and 54 Gy were prescribed for R0, R1, and R2 resected tumors, respectively. Recurrences were classified as in-field, marginal, or out-field. Prognostic factors were also evaluated. RESULTS: Seven recurrences were noted, including 2 in-field, 4 marginal, and 1 out-field, after a median follow-up of 60 months. In-field recurrences occurred in 1 patient who received 40.5 Gy of salvage RT after postoperative recurrence and another who received 45 Gy for R1 resection after multiple prior operations. All marginal failures were due to insufficient clinical target volume (CTV) margins regardless of dose (3 with 45 Gy and 1 with 54 Gy). On multivariate analysis, a CTV margin ≥5 cm and dose >45 Gy were significant predictors of non-recurrence (p = 0.039 and 0.049, respectively). Subgroup analysis showed that patients with both an CTV margin ≥5 cm and a dose >45 Gy showed a favorable outcome. CONCLUSIONS: RT is a valuable option for treating aggressive fibromatosis; doses ≥45 Gy and a large field produce optimal results. For in-field control, a higher dose is more necessary for gross residual tumors than for totally excised lesions. Public Library of Science 2018-05-29 /pmc/articles/PMC5973595/ /pubmed/29813130 http://dx.doi.org/10.1371/journal.pone.0198134 Text en © 2018 Choi 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
Choi, Seo Hee
Yoon, Hong In
Kim, Seung Hyun
Kim, Sang Kyum
Shin, Kyoo-Ho
Suh, Chang-Ok
Optimal radiotherapy strategy for primary or recurrent fibromatosis and long-term results
title Optimal radiotherapy strategy for primary or recurrent fibromatosis and long-term results
title_full Optimal radiotherapy strategy for primary or recurrent fibromatosis and long-term results
title_fullStr Optimal radiotherapy strategy for primary or recurrent fibromatosis and long-term results
title_full_unstemmed Optimal radiotherapy strategy for primary or recurrent fibromatosis and long-term results
title_short Optimal radiotherapy strategy for primary or recurrent fibromatosis and long-term results
title_sort optimal radiotherapy strategy for primary or recurrent fibromatosis and long-term results
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973595/
https://www.ncbi.nlm.nih.gov/pubmed/29813130
http://dx.doi.org/10.1371/journal.pone.0198134
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