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Combination of lymphocyte count and albumin concentration as a new prognostic biomarker for rectal cancer

Although numerous studies have highlighted the prognostic values of various inflammation-related markers, clinical significance remains to be elucidated. The prognostic values of inflammation-related biomarkers for rectal cancer were investigated in this study. A total of 448 patients with stage II/...

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Autores principales: Yamamoto, Takehito, Kawada, Kenji, Hida, Koya, Matsusue, Ryo, Itatani, Yoshiro, Mizuno, Rei, Yamaguchi, Takashi, Ikai, Iwao, Sakai, Yoshiharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930240/
https://www.ncbi.nlm.nih.gov/pubmed/33658561
http://dx.doi.org/10.1038/s41598-021-84475-4
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author Yamamoto, Takehito
Kawada, Kenji
Hida, Koya
Matsusue, Ryo
Itatani, Yoshiro
Mizuno, Rei
Yamaguchi, Takashi
Ikai, Iwao
Sakai, Yoshiharu
author_facet Yamamoto, Takehito
Kawada, Kenji
Hida, Koya
Matsusue, Ryo
Itatani, Yoshiro
Mizuno, Rei
Yamaguchi, Takashi
Ikai, Iwao
Sakai, Yoshiharu
author_sort Yamamoto, Takehito
collection PubMed
description Although numerous studies have highlighted the prognostic values of various inflammation-related markers, clinical significance remains to be elucidated. The prognostic values of inflammation-related biomarkers for rectal cancer were investigated in this study. A total of 448 patients with stage II/III rectal cancer undergoing curative resection were enrolled from the discovery cohort (n = 240) and validation cohort (n = 208). We comprehensively compared the prognostic values of 11 inflammation-related markers-derived from neutrophil, lymphocyte, platelet, monocyte, albumin, and C-reactive protein for overall survival (OS) and recurrence-free survival (RFS). Among 11 inflammation-related markers, only “lymphocyte × albumin (LA)” was significantly associated with both OS and RFS in the discovery cohort (P = 0.007 and 0.015, respectively). Multivariate analysis indicated that low LA was significantly associated with poor OS (hazard ratio [HR] 2.19, 95% confidence interval [CI] 1.09–4.58, P = 0.025), and poor RFS (HR 1.61, 95% CI 1.01–2.80, P = 0.048). Furthermore, using the discovery cohort, we confirmed that low LA was significantly associated with poor OS (HR 2.89, 95% CI 1.42–6.00, P = 0.002), and poor RFS (HR 1.79, 95% CI 1.04–2.95, P = 0.034). LA can be a novel prognostic biomarker for stage II/III rectal cancer.
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spelling pubmed-79302402021-03-05 Combination of lymphocyte count and albumin concentration as a new prognostic biomarker for rectal cancer Yamamoto, Takehito Kawada, Kenji Hida, Koya Matsusue, Ryo Itatani, Yoshiro Mizuno, Rei Yamaguchi, Takashi Ikai, Iwao Sakai, Yoshiharu Sci Rep Article Although numerous studies have highlighted the prognostic values of various inflammation-related markers, clinical significance remains to be elucidated. The prognostic values of inflammation-related biomarkers for rectal cancer were investigated in this study. A total of 448 patients with stage II/III rectal cancer undergoing curative resection were enrolled from the discovery cohort (n = 240) and validation cohort (n = 208). We comprehensively compared the prognostic values of 11 inflammation-related markers-derived from neutrophil, lymphocyte, platelet, monocyte, albumin, and C-reactive protein for overall survival (OS) and recurrence-free survival (RFS). Among 11 inflammation-related markers, only “lymphocyte × albumin (LA)” was significantly associated with both OS and RFS in the discovery cohort (P = 0.007 and 0.015, respectively). Multivariate analysis indicated that low LA was significantly associated with poor OS (hazard ratio [HR] 2.19, 95% confidence interval [CI] 1.09–4.58, P = 0.025), and poor RFS (HR 1.61, 95% CI 1.01–2.80, P = 0.048). Furthermore, using the discovery cohort, we confirmed that low LA was significantly associated with poor OS (HR 2.89, 95% CI 1.42–6.00, P = 0.002), and poor RFS (HR 1.79, 95% CI 1.04–2.95, P = 0.034). LA can be a novel prognostic biomarker for stage II/III rectal cancer. Nature Publishing Group UK 2021-03-03 /pmc/articles/PMC7930240/ /pubmed/33658561 http://dx.doi.org/10.1038/s41598-021-84475-4 Text en © The Author(s) 2021 Open Access This 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/.
spellingShingle Article
Yamamoto, Takehito
Kawada, Kenji
Hida, Koya
Matsusue, Ryo
Itatani, Yoshiro
Mizuno, Rei
Yamaguchi, Takashi
Ikai, Iwao
Sakai, Yoshiharu
Combination of lymphocyte count and albumin concentration as a new prognostic biomarker for rectal cancer
title Combination of lymphocyte count and albumin concentration as a new prognostic biomarker for rectal cancer
title_full Combination of lymphocyte count and albumin concentration as a new prognostic biomarker for rectal cancer
title_fullStr Combination of lymphocyte count and albumin concentration as a new prognostic biomarker for rectal cancer
title_full_unstemmed Combination of lymphocyte count and albumin concentration as a new prognostic biomarker for rectal cancer
title_short Combination of lymphocyte count and albumin concentration as a new prognostic biomarker for rectal cancer
title_sort combination of lymphocyte count and albumin concentration as a new prognostic biomarker for rectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930240/
https://www.ncbi.nlm.nih.gov/pubmed/33658561
http://dx.doi.org/10.1038/s41598-021-84475-4
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