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Prognostic role of tumor-infiltrating lymphocytes in gastric cancer: a meta-analysis
BACKGROUND: In patients with gastric cancer, the prognostic value of tumor-infiltrating lymphocytes (TILs) is still controversial. A meta-analysis was performed to evaluate the prognostic value of TILs in gastric cancer. MATERIALS AND METHODS: We identify studies from PubMed, Embase and the Cochrane...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593650/ https://www.ncbi.nlm.nih.gov/pubmed/28915679 http://dx.doi.org/10.18632/oncotarget.18065 |
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author | Zheng, Xiao Song, Xing Shao, Yingjie Xu, Bin Chen, Lujun Zhou, Qi Hu, Wenwei Zhang, Dachuan Wu, Changping Tao, Min Zhu, Yibei Jiang, Jingting |
author_facet | Zheng, Xiao Song, Xing Shao, Yingjie Xu, Bin Chen, Lujun Zhou, Qi Hu, Wenwei Zhang, Dachuan Wu, Changping Tao, Min Zhu, Yibei Jiang, Jingting |
author_sort | Zheng, Xiao |
collection | PubMed |
description | BACKGROUND: In patients with gastric cancer, the prognostic value of tumor-infiltrating lymphocytes (TILs) is still controversial. A meta-analysis was performed to evaluate the prognostic value of TILs in gastric cancer. MATERIALS AND METHODS: We identify studies from PubMed, Embase and the Cochrane Library to assess the prognostic effect of TILs in patients with gastric cancer. Fixed-effects models or random-effects models were used estimate the pooled hazard ratios (HRs) for overall survival (OS) and disease-free survival (DFS), which depend on the heterogeneity. RESULTS: A total of 31 observational studies including 4,185 patients were enrolled. For TILs subsets, the amount of CD8(+), FOXP3(+), CD3(+), CD57(+), CD20(+), CD45RO(+), Granzyme B(+) and T-bet(+) lymphocytes was significantly associated with improved survival (P < 0.05); moreover, the amount of CD3+ TILs in intra-tumoral compartment (IT) was the most significant prognostic marker (pooled HR = 0.52; 95% CI = 0.43–0.63; P < 0.001). However, CD4(+) TILs was not statistically associated with patients’ survival. FOXP3+ TILs showed bidirectional prognostic roles which had positive effect in IT (pooled HR = 1.57; 95% CI = 1.04–2.37; P = 0.033) and negative effect in extra-tumoral compartment (ET) (pooled HR = 0.76; 95% CI = 0.60–0.96; P = 0.022). CONCLUSIONS: This meta-analysis suggests that some TIL subsets could serve as prognostic biomarkers in gastric cancer. High-quality randomized controlled trials are needed to decide if these TILs could serve as targets for immunotherapy in gastric cancer. |
format | Online Article Text |
id | pubmed-5593650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55936502017-09-14 Prognostic role of tumor-infiltrating lymphocytes in gastric cancer: a meta-analysis Zheng, Xiao Song, Xing Shao, Yingjie Xu, Bin Chen, Lujun Zhou, Qi Hu, Wenwei Zhang, Dachuan Wu, Changping Tao, Min Zhu, Yibei Jiang, Jingting Oncotarget Meta-Analysis BACKGROUND: In patients with gastric cancer, the prognostic value of tumor-infiltrating lymphocytes (TILs) is still controversial. A meta-analysis was performed to evaluate the prognostic value of TILs in gastric cancer. MATERIALS AND METHODS: We identify studies from PubMed, Embase and the Cochrane Library to assess the prognostic effect of TILs in patients with gastric cancer. Fixed-effects models or random-effects models were used estimate the pooled hazard ratios (HRs) for overall survival (OS) and disease-free survival (DFS), which depend on the heterogeneity. RESULTS: A total of 31 observational studies including 4,185 patients were enrolled. For TILs subsets, the amount of CD8(+), FOXP3(+), CD3(+), CD57(+), CD20(+), CD45RO(+), Granzyme B(+) and T-bet(+) lymphocytes was significantly associated with improved survival (P < 0.05); moreover, the amount of CD3+ TILs in intra-tumoral compartment (IT) was the most significant prognostic marker (pooled HR = 0.52; 95% CI = 0.43–0.63; P < 0.001). However, CD4(+) TILs was not statistically associated with patients’ survival. FOXP3+ TILs showed bidirectional prognostic roles which had positive effect in IT (pooled HR = 1.57; 95% CI = 1.04–2.37; P = 0.033) and negative effect in extra-tumoral compartment (ET) (pooled HR = 0.76; 95% CI = 0.60–0.96; P = 0.022). CONCLUSIONS: This meta-analysis suggests that some TIL subsets could serve as prognostic biomarkers in gastric cancer. High-quality randomized controlled trials are needed to decide if these TILs could serve as targets for immunotherapy in gastric cancer. Impact Journals LLC 2017-05-22 /pmc/articles/PMC5593650/ /pubmed/28915679 http://dx.doi.org/10.18632/oncotarget.18065 Text en Copyright: © 2017 Zheng et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Meta-Analysis Zheng, Xiao Song, Xing Shao, Yingjie Xu, Bin Chen, Lujun Zhou, Qi Hu, Wenwei Zhang, Dachuan Wu, Changping Tao, Min Zhu, Yibei Jiang, Jingting Prognostic role of tumor-infiltrating lymphocytes in gastric cancer: a meta-analysis |
title | Prognostic role of tumor-infiltrating lymphocytes in gastric cancer: a meta-analysis |
title_full | Prognostic role of tumor-infiltrating lymphocytes in gastric cancer: a meta-analysis |
title_fullStr | Prognostic role of tumor-infiltrating lymphocytes in gastric cancer: a meta-analysis |
title_full_unstemmed | Prognostic role of tumor-infiltrating lymphocytes in gastric cancer: a meta-analysis |
title_short | Prognostic role of tumor-infiltrating lymphocytes in gastric cancer: a meta-analysis |
title_sort | prognostic role of tumor-infiltrating lymphocytes in gastric cancer: a meta-analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593650/ https://www.ncbi.nlm.nih.gov/pubmed/28915679 http://dx.doi.org/10.18632/oncotarget.18065 |
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