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Baseline splenic volume as a biomarker for clinical outcome and circulating lymphocyte count in gastric cancer
BACKGROUND: The spleen is the largest peripheral lymphoid organ in the body. Studies have implicated the spleen in the development of cancer. However, it is unknown whether splenic volume (SV) is associated with the clinical outcome of gastric cancer. METHODS: Data of gastric cancer patients treated...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923954/ https://www.ncbi.nlm.nih.gov/pubmed/36793344 http://dx.doi.org/10.3389/fonc.2022.1065716 |
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author | Zeng, Ziyang Liu, Zhen Li, Jie Sun, Juan Ma, Mingwei Ye, Xin Yu, Jianchun Kang, Weiming |
author_facet | Zeng, Ziyang Liu, Zhen Li, Jie Sun, Juan Ma, Mingwei Ye, Xin Yu, Jianchun Kang, Weiming |
author_sort | Zeng, Ziyang |
collection | PubMed |
description | BACKGROUND: The spleen is the largest peripheral lymphoid organ in the body. Studies have implicated the spleen in the development of cancer. However, it is unknown whether splenic volume (SV) is associated with the clinical outcome of gastric cancer. METHODS: Data of gastric cancer patients treated with surgical resection were retrospectively analyzed. Patients were divided into three groups: underweight, normal-weight and overweight. Overall survival was compared in patients with high and low splenic volume. The correlation between splenic volume and peripheral immune cells were analyzed. RESULTS: Of 541 patients, 71.2% were male and the median age was 60. Underweight, normal-weight and overweight patients accounted for 5.4%, 62.3% and 32.3%, respectively. High splenic volume was associated with unfavorable prognosis across the three groups. In addition, the increase of splenic volume during neoadjuvant chemotherapy was not associated with prognosis. The baseline splenic volume was negatively correlated with lymphocytes (r=-0.21, p<0.001) and positively correlated with NLR (neutrophil-to-lymphocyte ratio) (r=0.24, p<0.001). In a group of patients (n=56), splenic volume was found to have negative correlation with CD4+T cells (r=-0.27, p=0.041) and NK cells (r=-0.30, p=0.025). CONCLUSIONS: The presence of high splenic volume is a biomarker of unfavorable prognosis and reduced circulating lymphocytes in gastric cancer. |
format | Online Article Text |
id | pubmed-9923954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99239542023-02-14 Baseline splenic volume as a biomarker for clinical outcome and circulating lymphocyte count in gastric cancer Zeng, Ziyang Liu, Zhen Li, Jie Sun, Juan Ma, Mingwei Ye, Xin Yu, Jianchun Kang, Weiming Front Oncol Oncology BACKGROUND: The spleen is the largest peripheral lymphoid organ in the body. Studies have implicated the spleen in the development of cancer. However, it is unknown whether splenic volume (SV) is associated with the clinical outcome of gastric cancer. METHODS: Data of gastric cancer patients treated with surgical resection were retrospectively analyzed. Patients were divided into three groups: underweight, normal-weight and overweight. Overall survival was compared in patients with high and low splenic volume. The correlation between splenic volume and peripheral immune cells were analyzed. RESULTS: Of 541 patients, 71.2% were male and the median age was 60. Underweight, normal-weight and overweight patients accounted for 5.4%, 62.3% and 32.3%, respectively. High splenic volume was associated with unfavorable prognosis across the three groups. In addition, the increase of splenic volume during neoadjuvant chemotherapy was not associated with prognosis. The baseline splenic volume was negatively correlated with lymphocytes (r=-0.21, p<0.001) and positively correlated with NLR (neutrophil-to-lymphocyte ratio) (r=0.24, p<0.001). In a group of patients (n=56), splenic volume was found to have negative correlation with CD4+T cells (r=-0.27, p=0.041) and NK cells (r=-0.30, p=0.025). CONCLUSIONS: The presence of high splenic volume is a biomarker of unfavorable prognosis and reduced circulating lymphocytes in gastric cancer. Frontiers Media S.A. 2023-01-30 /pmc/articles/PMC9923954/ /pubmed/36793344 http://dx.doi.org/10.3389/fonc.2022.1065716 Text en Copyright © 2023 Zeng, Liu, Li, Sun, Ma, Ye, Yu and Kang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Zeng, Ziyang Liu, Zhen Li, Jie Sun, Juan Ma, Mingwei Ye, Xin Yu, Jianchun Kang, Weiming Baseline splenic volume as a biomarker for clinical outcome and circulating lymphocyte count in gastric cancer |
title | Baseline splenic volume as a biomarker for clinical outcome and circulating lymphocyte count in gastric cancer |
title_full | Baseline splenic volume as a biomarker for clinical outcome and circulating lymphocyte count in gastric cancer |
title_fullStr | Baseline splenic volume as a biomarker for clinical outcome and circulating lymphocyte count in gastric cancer |
title_full_unstemmed | Baseline splenic volume as a biomarker for clinical outcome and circulating lymphocyte count in gastric cancer |
title_short | Baseline splenic volume as a biomarker for clinical outcome and circulating lymphocyte count in gastric cancer |
title_sort | baseline splenic volume as a biomarker for clinical outcome and circulating lymphocyte count in gastric cancer |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923954/ https://www.ncbi.nlm.nih.gov/pubmed/36793344 http://dx.doi.org/10.3389/fonc.2022.1065716 |
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