Table 1.

Clinicopathological characteristics of EBV+ nodal T- and NK-cell lymphoma

EBV+ nodal T- and NK-cell lymphomaP 
All cases N = 22 (n [%])TET2 mutations
Present n = 15 (n [%])Absent n = 7 (n [%])
Age at diagnosis (median [range]), y 68 (21-83) 68 (40-83) 59 (21-75) .037 
Age at diagnosis, >60 y 16/22 (73) 14/15 (93) 2/7 (29) .004 
Sex (male/female) 14/8 8/7 6/1 .19 
Performance status score of >1 10/19 (53) 8/13 (62) 2/6 (33) .35 
Clinical stage Ⅲ/Ⅳ 19/22 (86) 15/15 (100) 4/7 (57) .023 
B symptoms present 11/18 (61) 8/11 (73) 3/7 (43) .33 
Extranodal involvement at >1 site
 
1/22 (5) 1/15 (7) 0/7 (0) 1.0 
IPI high-intermediate/high 15/20 (75) 13/14 (93) 2/6 (33) .014 
Platelets <130 × 10⁹/L 15/20 (75) 11/13 (85) 4/7 (57) .29 
Serum LDH level greater than normal 19/21 (90) 14/14 (100) 5/7 (71) .10 
Morphology     
Centroblastoid 14/22 (64) 11/15 (73) 3/7 (43) .34 
Pleomorphic 6/22 (27) 2/15 (13) 4/7 (57) .054 
Mixed 2/22 (9) 2/15 (13) 0/7 (0) 1.0 
Immunophenotype     
Cytotoxic molecules 21/22 (95) 14/15 (93) 7/7 (100) 1.0 
CD4 2/21 (10) 2/15 (13) 0/6 (0) 1.0 
CD5 4/20 (20) 2/13 (15) 2/7 (29) .59 
CD8 15/21 (71) 12/15 (80) 3/6 (50) .29 
CD56 2/22 (9) 0/15 (0) 2/7 (29) .091 
nPD-L1 3/22 (14) 0/15 (0) 3/7 (43) .023 
miPD-L1 10/22 (45) 7/15 (47) 3/7 (43) 1.0 
TFH cell marker  3/20 (15) 2/14 (14) 1/6 (17) 1.0 
ICOS 1/22 (5) 1/15 (7) 0/7 (0) 1.0 
PD-1 3/22 (14) 2/15 (13) 1/7 (14) 1.0 
T-cell type  20/20 (100) 14/14 (100) 6/6 (100) 
EBV+ nodal T- and NK-cell lymphomaP 
All cases N = 22 (n [%])TET2 mutations
Present n = 15 (n [%])Absent n = 7 (n [%])
Age at diagnosis (median [range]), y 68 (21-83) 68 (40-83) 59 (21-75) .037 
Age at diagnosis, >60 y 16/22 (73) 14/15 (93) 2/7 (29) .004 
Sex (male/female) 14/8 8/7 6/1 .19 
Performance status score of >1 10/19 (53) 8/13 (62) 2/6 (33) .35 
Clinical stage Ⅲ/Ⅳ 19/22 (86) 15/15 (100) 4/7 (57) .023 
B symptoms present 11/18 (61) 8/11 (73) 3/7 (43) .33 
Extranodal involvement at >1 site
 
1/22 (5) 1/15 (7) 0/7 (0) 1.0 
IPI high-intermediate/high 15/20 (75) 13/14 (93) 2/6 (33) .014 
Platelets <130 × 10⁹/L 15/20 (75) 11/13 (85) 4/7 (57) .29 
Serum LDH level greater than normal 19/21 (90) 14/14 (100) 5/7 (71) .10 
Morphology     
Centroblastoid 14/22 (64) 11/15 (73) 3/7 (43) .34 
Pleomorphic 6/22 (27) 2/15 (13) 4/7 (57) .054 
Mixed 2/22 (9) 2/15 (13) 0/7 (0) 1.0 
Immunophenotype     
Cytotoxic molecules 21/22 (95) 14/15 (93) 7/7 (100) 1.0 
CD4 2/21 (10) 2/15 (13) 0/6 (0) 1.0 
CD5 4/20 (20) 2/13 (15) 2/7 (29) .59 
CD8 15/21 (71) 12/15 (80) 3/6 (50) .29 
CD56 2/22 (9) 0/15 (0) 2/7 (29) .091 
nPD-L1 3/22 (14) 0/15 (0) 3/7 (43) .023 
miPD-L1 10/22 (45) 7/15 (47) 3/7 (43) 1.0 
TFH cell marker  3/20 (15) 2/14 (14) 1/6 (17) 1.0 
ICOS 1/22 (5) 1/15 (7) 0/7 (0) 1.0 
PD-1 3/22 (14) 2/15 (13) 1/7 (14) 1.0 
T-cell type  20/20 (100) 14/14 (100) 6/6 (100) 

IPI, International Prognostic Index; LDH, lactate dehydrogenase; miPD-L1, microenvironmental PD-L1; nPD-L1, neoplastic programmed cell-death ligand 1.

TET2 mutations present vs absent.

All of the evaluable 20 cases were negative for CD10 and BCL6, and all 22 evaluable cases were negative for CXCL13.

Patients with T-cell type showed positivity for TCR protein expression and/or TCRγ rearrangement.

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