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Neutrophil-to-lymphocyte ratio is a prognostic factor for colon cancer: a propensity score analysis
BACKGROUND: A large number of patients suffer recurrence after curative resection, and mortality from colon cancer remains high. The role of systemic inflammatory response, as reflected by neutrophil-to-lymphocyte ratio (NLR), in cancer recurrence and death has been increasingly recognized. This stu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519490/ https://www.ncbi.nlm.nih.gov/pubmed/32977767 http://dx.doi.org/10.1186/s12885-020-07429-5 |
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author | Mazaki, Junichi Katsumata, Kenji Kasahara, Kenta Tago, Tomoya Wada, Takahiro Kuwabara, Hiroshi Enomoto, Masanobu Ishizaki, Tetsuo Nagakawa, Yuichi Tsuchida, Akihiko |
author_facet | Mazaki, Junichi Katsumata, Kenji Kasahara, Kenta Tago, Tomoya Wada, Takahiro Kuwabara, Hiroshi Enomoto, Masanobu Ishizaki, Tetsuo Nagakawa, Yuichi Tsuchida, Akihiko |
author_sort | Mazaki, Junichi |
collection | PubMed |
description | BACKGROUND: A large number of patients suffer recurrence after curative resection, and mortality from colon cancer remains high. The role of systemic inflammatory response, as reflected by neutrophil-to-lymphocyte ratio (NLR), in cancer recurrence and death has been increasingly recognized. This study aimed to analyze long-term oncologic outcomes of Stage II-III colon cancer to examine the prognostic value of NLR using a propensity score analysis. METHODS: A total of 375 patients with colon cancer underwent radical surgery between 2000 and 2014 at Tokyo Medical University Hospital. Long-term oncologic outcomes of these patients were evaluated according to NLR values. A cut-off NLR of 3.0 was used based on receiver operating characteristic curve analysis. Primary outcomes were overall survival (OS) and relapse-free survival (RFS). An analysis of outcomes according to tumor sidedness was also performed. RESULTS: Patients with lower NLR values (“lower NLR group”) were more likely to have lymph node metastasis compared to those with higher NLR values (“higher NLR group”) before case matching. After case matching, clinical outcomes were similar between the two groups. There were no significant differences in 5-year OS and 5-year RFS rates between the two groups before case matching based on propensity scores. After case matching, 5-year OS rates were 94.5% in the lower NLR group (n = 135) and 87.0% in the higher NLR group (n = 135), showing a significant difference (p = 0.042). Five-year RFS rates were 87.8% in the lower NLR group and 77.9% in the higher NLR group, also showing a significant difference (p = 0.032). Among patients with left-sided colon cancer in the matched cohort, 5-year OS and 5-year RFS rates were 95.2 and 87.3% in the lower NLR group (n = 88), respectively, and 86.4 and 79.2% in the higher NLR group (n = 71), respectively, showing significant differences (p = 0.014 and p = 0.047, respectively). CONCLUSIONS: The NLR is an important prognostic factor for advanced colon cancer, especially for left-sided colon cancer. |
format | Online Article Text |
id | pubmed-7519490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75194902020-09-29 Neutrophil-to-lymphocyte ratio is a prognostic factor for colon cancer: a propensity score analysis Mazaki, Junichi Katsumata, Kenji Kasahara, Kenta Tago, Tomoya Wada, Takahiro Kuwabara, Hiroshi Enomoto, Masanobu Ishizaki, Tetsuo Nagakawa, Yuichi Tsuchida, Akihiko BMC Cancer Research Article BACKGROUND: A large number of patients suffer recurrence after curative resection, and mortality from colon cancer remains high. The role of systemic inflammatory response, as reflected by neutrophil-to-lymphocyte ratio (NLR), in cancer recurrence and death has been increasingly recognized. This study aimed to analyze long-term oncologic outcomes of Stage II-III colon cancer to examine the prognostic value of NLR using a propensity score analysis. METHODS: A total of 375 patients with colon cancer underwent radical surgery between 2000 and 2014 at Tokyo Medical University Hospital. Long-term oncologic outcomes of these patients were evaluated according to NLR values. A cut-off NLR of 3.0 was used based on receiver operating characteristic curve analysis. Primary outcomes were overall survival (OS) and relapse-free survival (RFS). An analysis of outcomes according to tumor sidedness was also performed. RESULTS: Patients with lower NLR values (“lower NLR group”) were more likely to have lymph node metastasis compared to those with higher NLR values (“higher NLR group”) before case matching. After case matching, clinical outcomes were similar between the two groups. There were no significant differences in 5-year OS and 5-year RFS rates between the two groups before case matching based on propensity scores. After case matching, 5-year OS rates were 94.5% in the lower NLR group (n = 135) and 87.0% in the higher NLR group (n = 135), showing a significant difference (p = 0.042). Five-year RFS rates were 87.8% in the lower NLR group and 77.9% in the higher NLR group, also showing a significant difference (p = 0.032). Among patients with left-sided colon cancer in the matched cohort, 5-year OS and 5-year RFS rates were 95.2 and 87.3% in the lower NLR group (n = 88), respectively, and 86.4 and 79.2% in the higher NLR group (n = 71), respectively, showing significant differences (p = 0.014 and p = 0.047, respectively). CONCLUSIONS: The NLR is an important prognostic factor for advanced colon cancer, especially for left-sided colon cancer. BioMed Central 2020-09-25 /pmc/articles/PMC7519490/ /pubmed/32977767 http://dx.doi.org/10.1186/s12885-020-07429-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Mazaki, Junichi Katsumata, Kenji Kasahara, Kenta Tago, Tomoya Wada, Takahiro Kuwabara, Hiroshi Enomoto, Masanobu Ishizaki, Tetsuo Nagakawa, Yuichi Tsuchida, Akihiko Neutrophil-to-lymphocyte ratio is a prognostic factor for colon cancer: a propensity score analysis |
title | Neutrophil-to-lymphocyte ratio is a prognostic factor for colon cancer: a propensity score analysis |
title_full | Neutrophil-to-lymphocyte ratio is a prognostic factor for colon cancer: a propensity score analysis |
title_fullStr | Neutrophil-to-lymphocyte ratio is a prognostic factor for colon cancer: a propensity score analysis |
title_full_unstemmed | Neutrophil-to-lymphocyte ratio is a prognostic factor for colon cancer: a propensity score analysis |
title_short | Neutrophil-to-lymphocyte ratio is a prognostic factor for colon cancer: a propensity score analysis |
title_sort | neutrophil-to-lymphocyte ratio is a prognostic factor for colon cancer: a propensity score analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519490/ https://www.ncbi.nlm.nih.gov/pubmed/32977767 http://dx.doi.org/10.1186/s12885-020-07429-5 |
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