Digitalni repozitorij raziskovalnih organizacij Slovenije

Izpis gradiva
A+ | A- | Pomoč | SLO | ENG

Naslov: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
Avtorji:ID Čas Slak, Teja (Avtor)
ID Miceska, Simona (Avtor)
ID Gašljević, Gorana (Avtor)
ID Boltežar, Lučka (Avtor)
ID Kloboves-Prevodnik, Veronika (Avtor)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (1,03 MB)
MD5: A8AD1398F2E438E7046399F441E858F0
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo DRO - Društvo radiologije in onkologije
Logo OI - Onkološki inštitut Ljubljana
Povzetek: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.
Ključne besede:diffuse large b-cell lymphoma, immunohistochemistry, cytopathology
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Datum objave:01.03.2024
Založnik:Association of Radiology and Oncology
Leto izida:2024
Št. strani:str. 99-109, X
Številčenje:Vol. 58, no. 1
Izvor:Ljubljana
PID:20.500.12556/DiRROS-30472 Novo okno
UDK:616-07
ISSN pri članku:1318-2099
DOI:10.2478/raon-2024-0010 Novo okno
COBISS.SI-ID:189584899 Novo okno
Datum objave v DiRROS:26.06.2026
Število ogledov:155
Število prenosov:70
Metapodatki:XML DC-XML DC-RDF
:
Kopiraj citat
  
Objavi na:Bookmark and Share


Postavite miškin kazalec na naslov za izpis povzetka. Klik na naslov izpiše podrobnosti ali sproži prenos.

Gradivo je del revije

Naslov:Radiology and oncology
Skrajšan naslov:Radiol. oncol.
Založnik:Slovenian Medical Society - Section of Radiology, Croatian Medical Association - Croatian Society of Radiology
ISSN:1318-2099
COBISS.SI-ID:32649472 Novo okno

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Naslov:Napovedna vrednost izražanja receptorja programirane celične smrti 1 in njegovega liganda na limfomskih celicah in tumorsko-imunskih celicah pri difuznem velikoceličnem B-celičnem limfomu, brez drugih oznak
Ključne besede:difuzni velikocelični limfom B, imunohistokemija, citopatologija


Nazaj