Soluble PD-L1 is associated with local and systemic inflammation markers in primary and secondary brain tumours

BackgroundImmune-modulatory treatments have so far shown limited clinical activity in primary brain tumours. We aimed to investigate soluble programmed death receptor ligand 1 (sPD-L1) as systemic inflammation parameter in patients with brain tumour.MethodsEDTA plasma was collected from 81 glioma (5...

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Veröffentlicht in:ESMO open 2020-11, Vol.5 (6), p.e000863-e000863, Article e000863
Hauptverfasser: Mair, Maximilian J, Pajenda, Sahra, Ilhan-Mutlu, Aysegül, Steindl, Ariane, Kiesel, Barbara, Widhalm, Georg, Dieckmann, Karin, Feldmann, Katharina, Hainfellner, Johannes, Marosi, Christine, Müllauer, Leonhard, Wagner, Ludwig, Preusser, Matthias, Berghoff, Anna S
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Sprache:eng
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Zusammenfassung:BackgroundImmune-modulatory treatments have so far shown limited clinical activity in primary brain tumours. We aimed to investigate soluble programmed death receptor ligand 1 (sPD-L1) as systemic inflammation parameter in patients with brain tumour.MethodsEDTA plasma was collected from 81 glioma (55 glioblastoma (GBM), 26 lower-grade glioma (LGG)), 17 meningioma and 44 brain metastasis (BM) patients and 24 controls. sPD-L1 concentrations were determined by ELISA. Correlations with the local tumour microenvironment were assessed by immunohistochemical analysis for PD-L1, CD3 and CD8.ResultssPD-L1 was detected in 62 out of 166 (37.7%) patients (glioma: 41/81, 50.6%; meningioma: 5/17, 29.4%; BM: 7/44, 15.9%; controls: 9/24, 37.5%; p=0.002). sPD-L1 concentrations were lower in BM than in LGG (p=0.003) or GBM (p
ISSN:2059-7029
2059-7029
DOI:10.1136/esmoopen-2020-000863