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High-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements with diffuse large B-cell lymphoma morphology.

Authors :
Scott DW
King RL
Staiger AM
Ben-Neriah S
Jiang A
Horn H
Mottok A
Farinha P
Slack GW
Ennishi D
Schmitz N
Pfreundschuh M
Nowakowski GS
Kahl BS
Connors JM
Gascoyne RD
Ott G
Macon WR
Rosenwald A
Source :
Blood [Blood] 2018 May 03; Vol. 131 (18), pp. 2060-2064. Date of Electronic Publication: 2018 Feb 23.
Publication Year :
2018

Abstract

High-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements (HGBL-DH/TH) is a newly defined entity in the latest World Health Organization Classification. Accurate diagnosis would appear to mandate fluorescence in situ hybridization (FISH) for all tumors with diffuse large B-cell lymphoma (DLBCL) morphology. We present the results of FISH, cell-of-origin, and immunohistochemistry (IHC) testing from 1228 DLBCL biopsies from 3 clinical trials and a population-based registry. HGBL-DH/TH made up 7.9% of the DLBCL, confined primarily to the germinal center B-cell-like (GCB; 13.3%) compared with activated B-cell-like (ABC; 1.7%) subtype ( P < .001). HGBL-DH/TH with BCL2 rearrangement is a GCB phenomenon with no cases observed in 415 ABC DLBCL. A screening strategy restricting FISH testing to tumors of GCB subtype (by Lymph2Cx or Hans IHC) plus dual protein expression of MYC and BCL2 by IHC could limit testing to 11% to 14% of tumors, with a positive predictive value of 30% to 37%; however, this strategy would miss approximately one-quarter of tumors with HBGL-DH/TH with BCL2 rearrangement and one-third of all HGBL-DH/TH. These results provide accurate estimation of the proportion of HGBL-DH/TH among tumors with DLBCL morphology and allow determination of the impact of various methods available to screen DLBCL tumors for FISH testing.<br /> (© 2018 by The American Society of Hematology.)

Details

Language :
English
ISSN :
1528-0020
Volume :
131
Issue :
18
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
29475959
Full Text :
https://doi.org/10.1182/blood-2017-12-820605