The Prognostic Value of CD206 in Solid Malignancies: A Systematic Review and Meta-Analysis.

CD206 macrophage polarization tumor associated macrophages

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
08 Jul 2021
Historique:
received: 10 06 2021
revised: 02 07 2021
accepted: 05 07 2021
entrez: 24 7 2021
pubmed: 25 7 2021
medline: 25 7 2021
Statut: epublish

Résumé

An increased presence of CD206-expressing tumor associated macrophages in solid cancers was proposed to be associated with worse outcomes in multiple types of malignancies, but contradictory results are published. We performed a reproducible systematic review and meta-analysis to provide increased evidence to confirm or reject this hypothesis following the Preferred Reporting Items for Systematic Reviews and Meta-analyses statement. The Embase, Web of Science, and MEDLINE-databases were systematically searched for eligible manuscripts. A total of 27 papers studying the prognostic impact of CD206 in 14 different tumor types were identified. Meta-analyses showed a significant impact on the overall survival (OS) and disease-free survival (DFS). While no significant differences were revealed in progression-free survival (PFS) and disease-specific survival (DSS), a shift towards negative survival was correlated with increased CD206-expresion. As a result of the different tumor types, large heterogeneity was present between the different tumor types. Subgroup analysis of hepatocellular carcinoma and gastric cancers revealed no heterogeneity, associated with a significant negative impact on OS in both groups. The current systematic review displays the increased presence CD206-expressing macrophages as a significant negative prognostic biomarker for both OS and DFS in patients diagnosed with solid cancers. Because a heterogenous group of tumor types was included in the meta-analysis, the results cannot be generalized. These results can, however, be used to further lead follow-up research to validate the specific prognostic value of CD206 in individual tumor types and therapeutic approaches.

Identifiants

pubmed: 34298638
pii: cancers13143422
doi: 10.3390/cancers13143422
pmc: PMC8305473
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Jens M Debacker (JM)

Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.
Department of Head and Neck Surgery, Ghent University Hospital, 9000 Ghent, Belgium.
Department of Nuclear Medicine, University Hospital Brussels, 1090 Brussels, Belgium.

Odrade Gondry (O)

Department of Nuclear Medicine, University Hospital Brussels, 1090 Brussels, Belgium.
In Vivo Cellular and Molecular Imaging, Vrije Universiteit Brussel, 1090 Brussels, Belgium.

Tony Lahoutte (T)

Department of Nuclear Medicine, University Hospital Brussels, 1090 Brussels, Belgium.
In Vivo Cellular and Molecular Imaging, Vrije Universiteit Brussel, 1090 Brussels, Belgium.

Marleen Keyaerts (M)

Department of Nuclear Medicine, University Hospital Brussels, 1090 Brussels, Belgium.
In Vivo Cellular and Molecular Imaging, Vrije Universiteit Brussel, 1090 Brussels, Belgium.

Wouter Huvenne (W)

Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.
Department of Head and Neck Surgery, Ghent University Hospital, 9000 Ghent, Belgium.

Classifications MeSH