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Molecular Subtypes and Genomic Profile of Primary Central Nervous System Lymphoma.

Authors :
Bödör C
Alpár D
Marosvári D
Galik B
Rajnai H
Bátai B
Nagy Á
Kajtár B
Burján A
Deák B
Schneider T
Alizadeh H
Matolcsy A
Brandner S
Storhoff J
Chen N
Liu M
Ghali N
Csala I
Bagó AG
Gyenesei A
Reiniger L
Source :
Journal of neuropathology and experimental neurology [J Neuropathol Exp Neurol] 2020 Feb 01; Vol. 79 (2), pp. 176-183.
Publication Year :
2020

Abstract

Primary central nervous system lymphomas (PCNSL) are aggressive non-Hodgkin lymphomas affecting the central nervous system (CNS). Although immunophenotyping studies suggested an uniform activated B-cell (ABC) origin, more recently a spectrum of ABC and germinal center B-cell (GC) cases has been proposed, with the molecular subtypes of PCNSL still being a matter of debate. With the emergence of novel therapies demonstrating different efficacy between the ABC and GC patient groups, precise assignment of molecular subtype is becoming indispensable. To determine the molecular subtype of 77 PCNSL and 17 secondary CNS lymphoma patients, we used the NanoString Lymphoma Subtyping Test (LST), a gene expression-based assay representing a more accurate technique of subtyping compared with standard immunohistochemical (IHC) algorithms. Mutational landscapes of 14 target genes were determined using ultra-deep next-generation sequencing. Using the LST-assay, a significantly lower proportion (80% vs 95%) of PCNSL cases displayed ABC phenotype compared with the IHC-based characterization. The most frequently mutated genes included MYD88, PIM1, and KMT2D. In summary, we successfully applied the LST-assay for molecular classification of PCNSL, reporting higher proportion of cases with GC phenotype compared with IHC analyses, leading to a more precise patient stratification potentially applicable in the diagnostic algorithm of PCNSL.<br /> (© 2019 American Association of Neuropathologists, Inc. All rights reserved.)

Details

Language :
English
ISSN :
1554-6578
Volume :
79
Issue :
2
Database :
MEDLINE
Journal :
Journal of neuropathology and experimental neurology
Publication Type :
Academic Journal
Accession number :
31886867
Full Text :
https://doi.org/10.1093/jnen/nlz125