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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>The prognostic significance of programmed cell death protein 1 and its ligand on lymphoma cells and tumor-immune cells in diffuse large B-cell lymphoma, not otherwise specified</dc:title><dc:creator>Čas Slak,	Teja	(Avtor)
	</dc:creator><dc:creator>Miceska,	Simona	(Avtor)
	</dc:creator><dc:creator>Gašljević,	Gorana	(Avtor)
	</dc:creator><dc:creator>Boltežar,	Lučka	(Avtor)
	</dc:creator><dc:creator>Kloboves-Prevodnik,	Veronika	(Avtor)
	</dc:creator><dc:subject>diffuse large b-cell lymphoma</dc:subject><dc:subject>immunohistochemistry</dc:subject><dc:subject>cytopathology</dc:subject><dc:description>Diffuse large B-cell lymphoma, not otherwise specified (DLBCL, NOS) is the most common type non-Hodgkin’s lymphoma, where the treatment of relapsed/refractory cases is the major challenge. Programmed cell death protein 1 (PD-1) and its ligand PD-L1 play a crucial role in the negative regulation of the immune response against the disease. The aim of the study was to analyze the expression of PD-1 and PD-L1 on lymphoma cells (LCs) and tumor-immune cells (TICs) and to investigate their correlation with outcome. Samples from 283 patients diagnosed with DLBCL, NOS (both germinal center B cell like [GCB] and non-GCB subtypes) were included in the study. Expression of PD-1 and PD-L1 was determined using double immunohistochemical staining (D-IHC) for PD-1/PAX5 and PD-L1/PAX5 on tissue microarrays. LCs were highlighted by D-IHC to obtain more accurate results. Clinical data and histologic diagnoses were obtained from electronic data records. We correlated clinical characteristics, and PD-1 and PD-L1 expression on LCs and TICs with progression-free survival (PFS) and overall survival (OS). Expression of PD-1 on TICs was observed in 38.4% and on LCs in 8.8% of cases, while PD-L1 was expressed on TICs in 46.8% and on LCs in 6.5% of cases. PD-L1 expression on LCs was more frequent in non-GCB subtype (p = 0.047). In addition, patients with PD-L1 expression on LCs had significantly shorter PFS (p = 0.015), and the expression retained significant in the multivariate model (p = 0.034). PD-L1 was more frequently expressed in LCs of the non-GCB subtype. Additionally, PD-L1 in LCs may predict shorter PFS time. D-IHC staining for PD-L1/PAX5 is a feasible method to assess PD-L1 expression on LCs of DLBCL, NOS patients and can be used to identify patients who may benefit from targeted immunotherapy with checkpoint inhibitors.</dc:description><dc:publisher>Association of Radiology and Oncology</dc:publisher><dc:date>2024</dc:date><dc:date>2026-06-26 14:10:09</dc:date><dc:type>Neznano</dc:type><dc:identifier>30472</dc:identifier><dc:identifier>UDK: 616-07</dc:identifier><dc:identifier>ISSN pri članku: 1318-2099</dc:identifier><dc:identifier>DOI: 10.2478/raon-2024-0010</dc:identifier><dc:identifier>COBISS_ID: 189584899</dc:identifier><dc:source>Ljubljana</dc:source><dc:language>sl</dc:language></metadata>
