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Strategy to avoid local recurrence in patients with locally advanced rectal cancer

BACKGROUND: To clarify the short- and long-term outcomes of radical surgery after neoadjuvant chemoradiotherapy (NCRT) with TS-1 and irinotecan, which enhances radiosensitivity, in patients with locally advanced rectal cancer. METHODS: The study group comprised 105 patients with locally advanced rec...

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Autores principales: Nakamura, Takatoshi, Sato, Takeo, Hayakawa, Kazushige, Koizumi, Wasaburou, Kumagai, Yuji, Watanabe, Masahiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438014/
https://www.ncbi.nlm.nih.gov/pubmed/30917848
http://dx.doi.org/10.1186/s13014-019-1253-9
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author Nakamura, Takatoshi
Sato, Takeo
Hayakawa, Kazushige
Koizumi, Wasaburou
Kumagai, Yuji
Watanabe, Masahiko
author_facet Nakamura, Takatoshi
Sato, Takeo
Hayakawa, Kazushige
Koizumi, Wasaburou
Kumagai, Yuji
Watanabe, Masahiko
author_sort Nakamura, Takatoshi
collection PubMed
description BACKGROUND: To clarify the short- and long-term outcomes of radical surgery after neoadjuvant chemoradiotherapy (NCRT) with TS-1 and irinotecan, which enhances radiosensitivity, in patients with locally advanced rectal cancer. METHODS: The study group comprised 105 patients with locally advanced rectal cancer who received NCRT followed by radical surgery. NCRT consisted of pelvic radiotherapy (45 Gy in 25 fractions over a period of 5 weeks), S-1 (80 mg/m(2)) given concurrently for 25 days, and irinotecan (60 mg/m(2)), given once a week as a continuous intravenous infusion. Radical surgery was performed 8 weeks after treatment. RESULTS: A pathological complete response was confirmed in 23.8%. The 5-year recurrence-free survival rate was 79.3%, and the 5-year overall survival rate was 87.1%. Multivariate analysis showed that the following 4 variables were independent predictors of recurrence-free survival: Sex (male: p = 0.0172), Pre-treatment tumor diameter (< 40 mm: p = 0.0223), Histopathological treatment response (grade 0,1: p = 0.0169), and ypN (ypN1: p = 0.1995; ypN2: p = 0.0007). Only ypN was an independent predictor of overall survival (ypN1: p = 0.0009; ypN2: p = 0.0012). CONCLUSIONS: Our treatment strategy combining TS-1 with irinotecan to increase radiosensitivity had a high response rate.
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spelling pubmed-64380142019-04-08 Strategy to avoid local recurrence in patients with locally advanced rectal cancer Nakamura, Takatoshi Sato, Takeo Hayakawa, Kazushige Koizumi, Wasaburou Kumagai, Yuji Watanabe, Masahiko Radiat Oncol Research BACKGROUND: To clarify the short- and long-term outcomes of radical surgery after neoadjuvant chemoradiotherapy (NCRT) with TS-1 and irinotecan, which enhances radiosensitivity, in patients with locally advanced rectal cancer. METHODS: The study group comprised 105 patients with locally advanced rectal cancer who received NCRT followed by radical surgery. NCRT consisted of pelvic radiotherapy (45 Gy in 25 fractions over a period of 5 weeks), S-1 (80 mg/m(2)) given concurrently for 25 days, and irinotecan (60 mg/m(2)), given once a week as a continuous intravenous infusion. Radical surgery was performed 8 weeks after treatment. RESULTS: A pathological complete response was confirmed in 23.8%. The 5-year recurrence-free survival rate was 79.3%, and the 5-year overall survival rate was 87.1%. Multivariate analysis showed that the following 4 variables were independent predictors of recurrence-free survival: Sex (male: p = 0.0172), Pre-treatment tumor diameter (< 40 mm: p = 0.0223), Histopathological treatment response (grade 0,1: p = 0.0169), and ypN (ypN1: p = 0.1995; ypN2: p = 0.0007). Only ypN was an independent predictor of overall survival (ypN1: p = 0.0009; ypN2: p = 0.0012). CONCLUSIONS: Our treatment strategy combining TS-1 with irinotecan to increase radiosensitivity had a high response rate. BioMed Central 2019-03-27 /pmc/articles/PMC6438014/ /pubmed/30917848 http://dx.doi.org/10.1186/s13014-019-1253-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Nakamura, Takatoshi
Sato, Takeo
Hayakawa, Kazushige
Koizumi, Wasaburou
Kumagai, Yuji
Watanabe, Masahiko
Strategy to avoid local recurrence in patients with locally advanced rectal cancer
title Strategy to avoid local recurrence in patients with locally advanced rectal cancer
title_full Strategy to avoid local recurrence in patients with locally advanced rectal cancer
title_fullStr Strategy to avoid local recurrence in patients with locally advanced rectal cancer
title_full_unstemmed Strategy to avoid local recurrence in patients with locally advanced rectal cancer
title_short Strategy to avoid local recurrence in patients with locally advanced rectal cancer
title_sort strategy to avoid local recurrence in patients with locally advanced rectal cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438014/
https://www.ncbi.nlm.nih.gov/pubmed/30917848
http://dx.doi.org/10.1186/s13014-019-1253-9
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