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Title:CD56-positive diffuse large B-cell lymphoma : comprehensive analysis of clinical, pathological, and molecular characteristics with literature review
Authors:ID Gašljević, Gorana (Author)
ID Boltežar, Lučka (Author)
ID Novaković, Srdjan (Author)
ID Šetrajčič Dragoš, Vita (Author)
ID Jezeršek Novaković, Barbara (Author)
ID Kloboves-Prevodnik, Veronika (Author)
Files:.pdf PDF - Presentation file, download (680,06 KB)
MD5: 78F2BF14295E33140E3AA7E2AC340883
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo OI - Institute of Oncology
Abstract:Diffuse large B-cell lymphoma (DLBCL) is the most common non-Hodgkin lymphoma. The expression of CD56 in DLBCL is highly unusual. Little is known about its incidence and clinical importance. So far, no genetic profiling was performed in CD56 positive DLBCL.Patients and methods. Tissue microarrays have been constructed, sectioned, and stained by H&E and immuno-histochemistry for 229 patients with DLBCL diagnosed 2008–2017. For CD56 positive cases, clinical data was collected including age at diagnosis, stage of the disease, International Prognostic Index (IPI) score, treatment scheme and number of chemotherapy cycles, radiation therapy, treatment outcome, and possible relapse of the disease. Overall survival (OS) and progression-free survival (PFS) were calculated. For four patients, RNA was extracted and targeted RNA (cDNA) sequencing of 125 genes was performed with the Archer FusionPlex Lymphoma kit.Results. CD56 expression was found in 7 cases (3%). The intensity of expression varied from weak to moderate focal, to very intensive and diffuse. All patients had de novo DLBCL. The median age at the time of diagnosis was 54.5 years. Five of them were women and 2 males. According to the Hans algorithm, 6 patients had the germinal centre B cells (GBC) type and one non-GBC (activated B-cell [ABC]) type, double expressor. Genetic profiling of four patients ac-cording to Schmitz’s classification showed that 1 case was of the BN2 subtype, 1 of EZB subtype, 2 were unclassified. The six treated patients reached a complete response and did not experience progression of the disease during the median follow-up period of 80.5 months.Conclusions. We report on one of the largest series of CD56+DLBCL with detailed clinicopathological data and for the first time described genetical findings in a limited number of patients. Our results show that CD56 expression is rare, but seems to be present in prognostic favourable subtypes of DLBCL not otherwise specified (NOS) as tested by immunohistochemical or genetic profiling
Keywords:diffuse large B-cell lymphoma, immunohistochemistry, lymphomas, CD56
Publication status:Published
Publication version:Version of Record
Publication date:01.06.2023
Publisher:Association of Radiology and Oncology
Year of publishing:2023
Number of pages:str. 249-256
Numbering:Vol. 57, no. 2
Source:Ljubljana
PID:20.500.12556/DiRROS-19829 New window
UDC:616-006.44
ISSN on article:1318-2099
DOI:10.2478/raon-2023-0016 New window
COBISS.SI-ID:147497731 New window
Copyright:by Authors
Publication date in DiRROS:25.07.2024
Views:16
Downloads:2
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Record is a part of a journal

Title:Radiology and oncology
Shortened title:Radiol. oncol.
Publisher:Slovenian Medical Society - Section of Radiology, Croatian Medical Association - Croatian Society of Radiology
ISSN:1318-2099
COBISS.SI-ID:32649472 New window

Secondary language

Language:Slovenian
Keywords:difuzni velikocelični limfom, imunohistokemija, limfomi, CD56


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