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Adjuvant therapy for T3N0 rectal cancer in the total mesorectal excision era- identification of the high risk patients

BACKGROUND: Adjuvant therapy for T3N0 rectal cancer was controversial with respect to both radiation and the use of a combined regimen of chemotherapy. We evaluated both clinical features and biomarkers and sought to determine risk factors for those patients retrospectively. METHODS: A total of 122...

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Autores principales: Zhu, Ji, Xu, Ye, Gu, Weilie, Peng, Junjie, Cai, Gang, Cai, Guoxiang, Sun, Wenjie, Shen, Weiqi, Cai, Sanjun, Zhang, Zhen
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009675/
https://www.ncbi.nlm.nih.gov/pubmed/21156077
http://dx.doi.org/10.1186/1748-717X-5-118
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author Zhu, Ji
Xu, Ye
Gu, Weilie
Peng, Junjie
Cai, Gang
Cai, Guoxiang
Sun, Wenjie
Shen, Weiqi
Cai, Sanjun
Zhang, Zhen
author_facet Zhu, Ji
Xu, Ye
Gu, Weilie
Peng, Junjie
Cai, Gang
Cai, Guoxiang
Sun, Wenjie
Shen, Weiqi
Cai, Sanjun
Zhang, Zhen
author_sort Zhu, Ji
collection PubMed
description BACKGROUND: Adjuvant therapy for T3N0 rectal cancer was controversial with respect to both radiation and the use of a combined regimen of chemotherapy. We evaluated both clinical features and biomarkers and sought to determine risk factors for those patients retrospectively. METHODS: A total of 122 patients with T3N0 rectal cancer were analyzed in this study from January 2000 to December 2005. Clinicopathologic and biomarkers were used to predict local recurrence (LR), disease-free survival (DFS), and overall survival (OS). RESULTS: The median follow-up interval was 45.4 months. Five-year LR, DFS, and OS rates were 10.4%, 68.3%, and 88.7%. Having a lower tumor location and showing low P21 and high CD44v6 expression were identified as risk factors for LR: patients with two or three of these risk factors had a higher 5-year LR rate (19.3%) than did patients with none or one of these risk factors (6.8%) (p = 0.05). A poorer DFS was related to low P21 nor high CD44v6 expression but not to tumor location: the 5-year DFS rates were 79.3% for those with neither, 65.9% for those with either one or the other, and 16.9% for those with both (p = 0.00). CONCLUSIONS: The prognostic model including tumor location, P21 and CD44v6 expressions could help to distinguish these patients with high risk T3N0 patients and determine whether adjuvant therapy was beneficial.
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spelling pubmed-30096752010-12-24 Adjuvant therapy for T3N0 rectal cancer in the total mesorectal excision era- identification of the high risk patients Zhu, Ji Xu, Ye Gu, Weilie Peng, Junjie Cai, Gang Cai, Guoxiang Sun, Wenjie Shen, Weiqi Cai, Sanjun Zhang, Zhen Radiat Oncol Research BACKGROUND: Adjuvant therapy for T3N0 rectal cancer was controversial with respect to both radiation and the use of a combined regimen of chemotherapy. We evaluated both clinical features and biomarkers and sought to determine risk factors for those patients retrospectively. METHODS: A total of 122 patients with T3N0 rectal cancer were analyzed in this study from January 2000 to December 2005. Clinicopathologic and biomarkers were used to predict local recurrence (LR), disease-free survival (DFS), and overall survival (OS). RESULTS: The median follow-up interval was 45.4 months. Five-year LR, DFS, and OS rates were 10.4%, 68.3%, and 88.7%. Having a lower tumor location and showing low P21 and high CD44v6 expression were identified as risk factors for LR: patients with two or three of these risk factors had a higher 5-year LR rate (19.3%) than did patients with none or one of these risk factors (6.8%) (p = 0.05). A poorer DFS was related to low P21 nor high CD44v6 expression but not to tumor location: the 5-year DFS rates were 79.3% for those with neither, 65.9% for those with either one or the other, and 16.9% for those with both (p = 0.00). CONCLUSIONS: The prognostic model including tumor location, P21 and CD44v6 expressions could help to distinguish these patients with high risk T3N0 patients and determine whether adjuvant therapy was beneficial. BioMed Central 2010-12-15 /pmc/articles/PMC3009675/ /pubmed/21156077 http://dx.doi.org/10.1186/1748-717X-5-118 Text en Copyright ©2010 Zhu et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Zhu, Ji
Xu, Ye
Gu, Weilie
Peng, Junjie
Cai, Gang
Cai, Guoxiang
Sun, Wenjie
Shen, Weiqi
Cai, Sanjun
Zhang, Zhen
Adjuvant therapy for T3N0 rectal cancer in the total mesorectal excision era- identification of the high risk patients
title Adjuvant therapy for T3N0 rectal cancer in the total mesorectal excision era- identification of the high risk patients
title_full Adjuvant therapy for T3N0 rectal cancer in the total mesorectal excision era- identification of the high risk patients
title_fullStr Adjuvant therapy for T3N0 rectal cancer in the total mesorectal excision era- identification of the high risk patients
title_full_unstemmed Adjuvant therapy for T3N0 rectal cancer in the total mesorectal excision era- identification of the high risk patients
title_short Adjuvant therapy for T3N0 rectal cancer in the total mesorectal excision era- identification of the high risk patients
title_sort adjuvant therapy for t3n0 rectal cancer in the total mesorectal excision era- identification of the high risk patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009675/
https://www.ncbi.nlm.nih.gov/pubmed/21156077
http://dx.doi.org/10.1186/1748-717X-5-118
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