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Prognostic significance of immune cells in non-small cell lung cancer: meta-analysis
BACKGROUND: Tumor-associated immune cells are prognostic in non-small cell lung cancer (NSCLC) but findings have been conflicting. OBJECTIVES: To determine the prognostic role of immune cells according to localization in NSCLC patients. METHODS: A systematic literature review and meta-analysis was p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973851/ https://www.ncbi.nlm.nih.gov/pubmed/29872507 http://dx.doi.org/10.18632/oncotarget.24835 |
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author | Soo, Ross A. Chen, Zhaojin Yan Teng, Rebecca Siew Tan, Hon-Lyn Iacopetta, Barry Tai, Bee Choo Soong, Richie |
author_facet | Soo, Ross A. Chen, Zhaojin Yan Teng, Rebecca Siew Tan, Hon-Lyn Iacopetta, Barry Tai, Bee Choo Soong, Richie |
author_sort | Soo, Ross A. |
collection | PubMed |
description | BACKGROUND: Tumor-associated immune cells are prognostic in non-small cell lung cancer (NSCLC) but findings have been conflicting. OBJECTIVES: To determine the prognostic role of immune cells according to localization in NSCLC patients. METHODS: A systematic literature review and meta-analysis was performed on dendritic cell (DC), tumor associated macrophages (TAM), mast cells (MC), natural killer (NK) cells, T and B cells and tumor CTLA-4 and PD-L1 studies. RESULTS: We analysed 96 articles (n= 21,752 patients). Improved outcomes were seen with increased tumor DCs (overall survival (OS) hazard ratio (HR) 0.55; 95% confidence interval (CI) 0.44–0.68), NK cells (OS HR 0.45; 0.31–0.65), TAMs (OS HR 0.33; 0.17–0.62), M1 TAMs (OS HR 0.10; 0.05–0.21), CD3+ T cells (disease specific survival (DSS) HR 0.64; 0.48–0.86), CD8+ T cells (OS HR 0.78; 0.66–0.93), B cells (OS HR 0.65; 0.42–0.99) and with increased stroma DC (DSS HR 0.62; 0.47–0.83), NK cells (DSS HR 0.51; 0.32–0.82), M1 TAMs (OS HR 0.63; 0.42–0.94), CD4+ T cells (OS HR 0.45; 0.21–0.94), CD8+ T cells (OS HR 0.77; 0.69–0.86) and B cells (OS HR 0.74;0.56–0.99). Poor outcomes were seen with stromal M2 TAMs (OS HR 1.44; 1.06–1.96) and Tregs (relapse free survival (RFS) HR 1.80; 1.34–2.43). Tumor PD-L1 was associated with worse OS (1.40; 1.20–1.69), RFS (1.67) and DFS (1.24). CONCLUSION: Tumor and stroma DC, NK cells, M1 TAMs, CD8+ T cells and B cells were associated with improved prognosis and tumor PD-L1, stromal M2 TAMs and Treg cells had poorer prognosis. Higher quality studies are required for confirmation. |
format | Online Article Text |
id | pubmed-5973851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-59738512018-06-05 Prognostic significance of immune cells in non-small cell lung cancer: meta-analysis Soo, Ross A. Chen, Zhaojin Yan Teng, Rebecca Siew Tan, Hon-Lyn Iacopetta, Barry Tai, Bee Choo Soong, Richie Oncotarget Meta-Analysis BACKGROUND: Tumor-associated immune cells are prognostic in non-small cell lung cancer (NSCLC) but findings have been conflicting. OBJECTIVES: To determine the prognostic role of immune cells according to localization in NSCLC patients. METHODS: A systematic literature review and meta-analysis was performed on dendritic cell (DC), tumor associated macrophages (TAM), mast cells (MC), natural killer (NK) cells, T and B cells and tumor CTLA-4 and PD-L1 studies. RESULTS: We analysed 96 articles (n= 21,752 patients). Improved outcomes were seen with increased tumor DCs (overall survival (OS) hazard ratio (HR) 0.55; 95% confidence interval (CI) 0.44–0.68), NK cells (OS HR 0.45; 0.31–0.65), TAMs (OS HR 0.33; 0.17–0.62), M1 TAMs (OS HR 0.10; 0.05–0.21), CD3+ T cells (disease specific survival (DSS) HR 0.64; 0.48–0.86), CD8+ T cells (OS HR 0.78; 0.66–0.93), B cells (OS HR 0.65; 0.42–0.99) and with increased stroma DC (DSS HR 0.62; 0.47–0.83), NK cells (DSS HR 0.51; 0.32–0.82), M1 TAMs (OS HR 0.63; 0.42–0.94), CD4+ T cells (OS HR 0.45; 0.21–0.94), CD8+ T cells (OS HR 0.77; 0.69–0.86) and B cells (OS HR 0.74;0.56–0.99). Poor outcomes were seen with stromal M2 TAMs (OS HR 1.44; 1.06–1.96) and Tregs (relapse free survival (RFS) HR 1.80; 1.34–2.43). Tumor PD-L1 was associated with worse OS (1.40; 1.20–1.69), RFS (1.67) and DFS (1.24). CONCLUSION: Tumor and stroma DC, NK cells, M1 TAMs, CD8+ T cells and B cells were associated with improved prognosis and tumor PD-L1, stromal M2 TAMs and Treg cells had poorer prognosis. Higher quality studies are required for confirmation. Impact Journals LLC 2018-05-15 /pmc/articles/PMC5973851/ /pubmed/29872507 http://dx.doi.org/10.18632/oncotarget.24835 Text en Copyright: © 2018 Soo et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Meta-Analysis Soo, Ross A. Chen, Zhaojin Yan Teng, Rebecca Siew Tan, Hon-Lyn Iacopetta, Barry Tai, Bee Choo Soong, Richie Prognostic significance of immune cells in non-small cell lung cancer: meta-analysis |
title | Prognostic significance of immune cells in non-small cell lung cancer: meta-analysis |
title_full | Prognostic significance of immune cells in non-small cell lung cancer: meta-analysis |
title_fullStr | Prognostic significance of immune cells in non-small cell lung cancer: meta-analysis |
title_full_unstemmed | Prognostic significance of immune cells in non-small cell lung cancer: meta-analysis |
title_short | Prognostic significance of immune cells in non-small cell lung cancer: meta-analysis |
title_sort | prognostic significance of immune cells in non-small cell lung cancer: meta-analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973851/ https://www.ncbi.nlm.nih.gov/pubmed/29872507 http://dx.doi.org/10.18632/oncotarget.24835 |
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