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. 2021 Nov 29;113(1):334–348. doi: 10.1111/cas.15179

TABLE 1.

Main pathological characteristics in patients with diffuse large B‐cell lymphoma (training set)

Characteristic Frequency (%)
Histological
CD3+ 0s (1.6)
CD5+ 12/129 (9.3)
CD20+ 129/131 (98.5)
CD10+ 39/130 (30.0)
BCL6+ 88/129 (68.2)
MUM1+ 89/129 (69.0)
Non‐GCB (Hans classifier) 82/129 (63.6)
BCL2+ 89/129 (69.0)
EBV EBER+ 10/125 (7.6)
RGS1‐high 64/108 (59.3)
MYC‐high 62/119 (52.1)
Molecular
BCL2 split (FISH) 13/121 (10.7)
MYC split (FISH) 13/124 (10.5)
BCL6 split (FISH) 18/106 (17.0)
BCL2 and MYC split (FISH) 2/119 (1.7)
BCL2 IHC+ and MYC‐IHC‐high (double expressor) 39/123 (31.7)
MYC t+ and/or MYC‐IHC‐high 67/132 (50.8)
High grade B‐cell lymphoma (MYC t+ and BCL2 t+ and/or BCL6 t+) 5/125 (4.0)
MYD88 L265P mutation 12/121 (9.9)

The cut‐off for positivity for the immunohistochemical (IHC) markers for B lymphocytes of DLBCL using the Hans algorithm (CD10, BCL6, IRF4/MUM1) was set at the conventional 30%. BCL2 was considered positive if more than 50% of the tumoral cells were positive. High regulator of G‐protein signaling 1 (RGS1) expression associates with poor prognosis in DLBCL. RGS1‐high corresponds to expression 2‐3+ as we have previously described. 21 MYC translocation positive cases positively correlated with higher IHC expression for MYC protein (Fisher’s exact test, P = .003); MYC‐high cut‐off was 40%, and after digital image quantification was set at 22%.

Abbreviations: EBER, EBV‐encoded small RNA; EBV, Epstein–Barr virus; GCB, germinal center B cell‐like.