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dc.contributor.authorMohamed, Nuha Mohamed Gaafar
dc.contributor.authorOsman, Tarig Al-Hadi
dc.contributor.authorElsheikh, Mariam
dc.contributor.authorAlhaj Ahmed, Israa Abdul Rhman Hassaballah
dc.contributor.authorDongre, Harsh Nitin
dc.contributor.authorFromreide, Siren
dc.contributor.authorSuleiman, Ahmed M.
dc.contributor.authorJohannessen, Anne Christine
dc.contributor.authorNginamau, Elisabeth Sivy
dc.contributor.authorCostea, Daniela Elena
dc.date.accessioned2022-12-12T09:43:35Z
dc.date.available2022-12-12T09:43:35Z
dc.date.created2022-10-25T13:17:10Z
dc.date.issued2022
dc.identifier.issn2057-4347
dc.identifier.urihttps://hdl.handle.net/11250/3037178
dc.description.abstractBackground We recently described the tumor immune microenvironment (TIME) in oral squamous cell carcinomas (OSCC) from Sudan by assessing the core of the lesions. However, the invasive tumor front (ITF) is the most active part of OSCC lesions; thus, TIME should also be characterized at the ITF in this patient cohort. Objectives We aimed to evaluate patterns of immune cell infiltration at the ITF in a cohort of OSCC patients from Sudan previously investigated at the tumor center and their association with clinicopathological parameters. Methods This study was performed on a prospective cohort of 22 OSCC patients attending Khartoum Dental Teaching Hospital with a median follow-up of 48 months. Inflammatory infiltrate densities of CD4-, CD8-, FoxP3-, CD20-, CD66b-, M1 (CD80/CD68)-, M2 (CD163/CD68)-, and PD-L1-positive cells were assessed at the ITF by immunohistochemistry, followed by digital quantitative analysis at the stromal and epithelial compartments separately. Histopathological parameters such as the worst pattern of invasion, differentiation, and tumor budding (TB) were also assessed. Correlations between clinicopathological parameters and survival analysis were investigated using SPSS. Results All inflammatory cell subsets investigated were found to be higher in the stromal compartment as compared to the epithelial one, except for the PD-L1+ subset. Stromal infiltration with the CD8+ cell subset was associated with low TB. Kaplan–Meier analyses identified higher epithelial and stromal CD4+ cell subsets. The presence of PD-L1 was found to be associated with unfavorable overall survival. Further, Cox's regression analysis using an age- and tumor-stage-adjusted model identified epithelial PD-L1 expression at the ITF as the only independent prognosticator. Conclusions Epithelial PD-L1 expression at the ITF was found to be an independent prognostic biomarker for OSCC in a cohort of Sudanese patients.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleEpithelial PD-L1 expression at tumor front predicts overall survival in a cohort of oral squamous cell carcinomas from Sudanen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1002/cre2.666
dc.identifier.cristin2064857
dc.source.journalClinical and Experimental Dental Researchen_US
dc.identifier.citationClinical and Experimental Dental Research. 2022.en_US


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