The prognostic effects of circulating myeloid-derived suppressor cells in non-small cell lung cancer: systematic review and meta-analysis

被引:0
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作者
Giuseppe Bronte
Luana Calabrò
Fabiola Olivieri
Antonio Domenico Procopio
Lucio Crinò
机构
[1] Università Politecnica Delle Marche,Department of Clinical and Molecular Sciences (DISCLIMO)
[2] National Institute of Health and Sciences On Ageing (IRCCS INRCA),Clinic of Laboratory and Precision Medicine
[3] University Hospital of Ferrara,Medical Oncology Unit
[4] IRCCS Istituto Romagnolo Per Lo Studio Dei Tumori (IRST) “Dino Amadori”,Department of Medical Oncology
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Myeloid-derived suppressor cells; Non-small cell lung cancer; Prognosis;
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摘要
Immunotherapy is the main standard treatment for non-small cell lung cancer (NSCLC) patients. Immune suppressive cells in tumor microenvironment can counteract its efficacy. Myeloid-derived suppressor cells (MDSCs) include two major subsets: polymorphonuclear (PMN-MDSCs) and monocytic (M-MDSCs). Many studies explored the prognostic impact of these cell populations in NSCLC patients. The aim of this systematic review is to select studies for a meta-analysis, which compares prognosis between patients with high vs low circulating MDSC levels. We collected hazard ratios (HRs) and relative 95% confidence intervals (CIs) in terms of progression-free survival (PFS) or recurrence-free survival (RFS), and overall survival (OS). Among 139 studies retrieved from literature search, 14 eligible studies (905 NSCLC patients) met inclusion criteria. Low circulating MDSC levels favor a better PFS/RFS (HR = 1.84; 95% CI = 1.28–2.65) and OS (HR = 1.78; 95% CI = 1.29–2.46). The subgroup analysis based on MDSC subtypes (total-, PMN-, and M-MDSCs) obtained a statistical significance only for M-MDSCs, both in terms of PFS/RFS (HR = 2.67; 95% CI = 2.04–3.50) and OS (HR = 2.10; 95% CI = 1.61–2.75). NSCLC patients bearing high M-MDSC levels in peripheral blood experience a worse prognosis than those with low levels, both in terms of PFS/RFS and OS. This finding suggests that detecting and targeting this MDSC subset could help to improve NSCLC treatment efficacy.
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页码:1551 / 1561
页数:10
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