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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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. |
format | Online Article Text |
id | pubmed-6438014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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