Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zeng, Ziyang, Liu, Zhen, Li, Jie, Sun, Juan, Ma, Mingwei, Ye, Xin, Yu, Jianchun, Kang, Weiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
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
_version_ 1784887808098304000
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
work_keys_str_mv AT zengziyang baselinesplenicvolumeasabiomarkerforclinicaloutcomeandcirculatinglymphocytecountingastriccancer
AT liuzhen baselinesplenicvolumeasabiomarkerforclinicaloutcomeandcirculatinglymphocytecountingastriccancer
AT lijie baselinesplenicvolumeasabiomarkerforclinicaloutcomeandcirculatinglymphocytecountingastriccancer
AT sunjuan baselinesplenicvolumeasabiomarkerforclinicaloutcomeandcirculatinglymphocytecountingastriccancer
AT mamingwei baselinesplenicvolumeasabiomarkerforclinicaloutcomeandcirculatinglymphocytecountingastriccancer
AT yexin baselinesplenicvolumeasabiomarkerforclinicaloutcomeandcirculatinglymphocytecountingastriccancer
AT yujianchun baselinesplenicvolumeasabiomarkerforclinicaloutcomeandcirculatinglymphocytecountingastriccancer
AT kangweiming baselinesplenicvolumeasabiomarkerforclinicaloutcomeandcirculatinglymphocytecountingastriccancer