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Clinical outcomes of chemoradiotherapy for locally recurrent rectal cancer
BACKGROUND: To assess the clinical outcome of chemoradiotherapy with or without surgery for locally recurrent rectal cancer (LRRC) and to find useful and significant prognostic factors for a clinical situation. METHODS: Between January 2001 and February 2009, 67 LRRC patients, who entered into concu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118124/ https://www.ncbi.nlm.nih.gov/pubmed/21595980 http://dx.doi.org/10.1186/1748-717X-6-51 |
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author | Lee, Joo Ho Kim, Dae Yong Kim, Sun Young Park, Ji Won Choi, Hyo Seong Oh, Jae Hwan Chang, Hee Jin Kim, Tae Hyun Park, Suk Won |
author_facet | Lee, Joo Ho Kim, Dae Yong Kim, Sun Young Park, Ji Won Choi, Hyo Seong Oh, Jae Hwan Chang, Hee Jin Kim, Tae Hyun Park, Suk Won |
author_sort | Lee, Joo Ho |
collection | PubMed |
description | BACKGROUND: To assess the clinical outcome of chemoradiotherapy with or without surgery for locally recurrent rectal cancer (LRRC) and to find useful and significant prognostic factors for a clinical situation. METHODS: Between January 2001 and February 2009, 67 LRRC patients, who entered into concurrent chemoradiotherapy with or without surgery, were reviewed retrospectively. Of the 67 patients, 45 were treated with chemoradiotherapy plus surgery, and the remaining 22 were treated with chemoradiotherapy alone. The mean radiation doses (biologically equivalent dose in 2-Gy fractions) were 54.6 Gy and 66.5 Gy for the chemoradiotherapy with and without surgery groups, respectively. RESULTS: The median survival duration of all patients was 59 months. Five-year overall (OS), relapse-free (RFS), locoregional relapse-free (LRFS), and distant metastasis-free survival (DMFS) were 48.9%, 31.6%, 66.4%, and 40.6%, respectively. A multivariate analysis demonstrated that the presence of symptoms was an independent prognostic factor influencing OS, RFS, LRFS, and DMFS. No statistically significant difference was found in OS (p = 0.181), RFS (p = 0.113), LRFS (p = 0.379), or DMFS (p = 0.335) when comparing clinical outcomes between the chemoradiotherapy with and without surgery groups. CONCLUSIONS: Chemoradiotherapy with or without surgery could be a potential option for an LRRC cure, and the symptoms related to LRRC were a significant prognostic factor predicting poor clinical outcome. The chemoradiotherapy scheme for LRRC patients should be adjusted to the possibility of resectability and risk of local failure to focus on local control. |
format | Online Article Text |
id | pubmed-3118124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31181242011-06-19 Clinical outcomes of chemoradiotherapy for locally recurrent rectal cancer Lee, Joo Ho Kim, Dae Yong Kim, Sun Young Park, Ji Won Choi, Hyo Seong Oh, Jae Hwan Chang, Hee Jin Kim, Tae Hyun Park, Suk Won Radiat Oncol Research BACKGROUND: To assess the clinical outcome of chemoradiotherapy with or without surgery for locally recurrent rectal cancer (LRRC) and to find useful and significant prognostic factors for a clinical situation. METHODS: Between January 2001 and February 2009, 67 LRRC patients, who entered into concurrent chemoradiotherapy with or without surgery, were reviewed retrospectively. Of the 67 patients, 45 were treated with chemoradiotherapy plus surgery, and the remaining 22 were treated with chemoradiotherapy alone. The mean radiation doses (biologically equivalent dose in 2-Gy fractions) were 54.6 Gy and 66.5 Gy for the chemoradiotherapy with and without surgery groups, respectively. RESULTS: The median survival duration of all patients was 59 months. Five-year overall (OS), relapse-free (RFS), locoregional relapse-free (LRFS), and distant metastasis-free survival (DMFS) were 48.9%, 31.6%, 66.4%, and 40.6%, respectively. A multivariate analysis demonstrated that the presence of symptoms was an independent prognostic factor influencing OS, RFS, LRFS, and DMFS. No statistically significant difference was found in OS (p = 0.181), RFS (p = 0.113), LRFS (p = 0.379), or DMFS (p = 0.335) when comparing clinical outcomes between the chemoradiotherapy with and without surgery groups. CONCLUSIONS: Chemoradiotherapy with or without surgery could be a potential option for an LRRC cure, and the symptoms related to LRRC were a significant prognostic factor predicting poor clinical outcome. The chemoradiotherapy scheme for LRRC patients should be adjusted to the possibility of resectability and risk of local failure to focus on local control. BioMed Central 2011-05-20 /pmc/articles/PMC3118124/ /pubmed/21595980 http://dx.doi.org/10.1186/1748-717X-6-51 Text en Copyright ©2011 Lee 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 Lee, Joo Ho Kim, Dae Yong Kim, Sun Young Park, Ji Won Choi, Hyo Seong Oh, Jae Hwan Chang, Hee Jin Kim, Tae Hyun Park, Suk Won Clinical outcomes of chemoradiotherapy for locally recurrent rectal cancer |
title | Clinical outcomes of chemoradiotherapy for locally recurrent rectal cancer |
title_full | Clinical outcomes of chemoradiotherapy for locally recurrent rectal cancer |
title_fullStr | Clinical outcomes of chemoradiotherapy for locally recurrent rectal cancer |
title_full_unstemmed | Clinical outcomes of chemoradiotherapy for locally recurrent rectal cancer |
title_short | Clinical outcomes of chemoradiotherapy for locally recurrent rectal cancer |
title_sort | clinical outcomes of chemoradiotherapy for locally recurrent rectal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118124/ https://www.ncbi.nlm.nih.gov/pubmed/21595980 http://dx.doi.org/10.1186/1748-717X-6-51 |
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