Table 1.

Patient characteristics

All patients (N = 78)AITL/TFH patients (n = 71)
Age median (IQR) 70 (67-73) 70 (67-73) 
Sex   
 Female 41 (53) 38 (53) 
 Male 37 (47) 33 (47) 
B symptoms 44/78 (56) 40/71 (56) 
Ann Arbor stage   
 I-II 5 (6) 5 (7) 
 III-IV 73 (94) 66 (93) 
Number of extranodal sites   
 0-1 40 (51) 38 (53) 
 >1 38 (49) 33 (47) 
ECOG performance status   
 0-1 61 (78) 54 (76) 
 2 17 (22) 17 (24) 
Bone marrow involvement 36/73 (49) 32/66 (48) 
Hypergammaglobulinemia 30/70 (43) 29/64 (45) 
Elevated LDH 42/77 (55) 39/70 (56) 
Histology   
 AITL 67 (94) 67 (86) 
 Nodal PTCL with TFH phenotype 4 (6) 4 (5) 
 Other* 7 (9) 0 (0) 
IPI   
 1-3 48 (62) 43 (61) 
 4-5 29 (38) 27 (39) 
PIT   
 0-2 50 (69) 45 (69) 
 3-4 22 (31) 20 (31) 
SUVmax median (IQR) 11 (7-18) 12 (7-18) 
TMTV median (IQR) 433 (127-937) 468 (125-942) 
All patients (N = 78)AITL/TFH patients (n = 71)
Age median (IQR) 70 (67-73) 70 (67-73) 
Sex   
 Female 41 (53) 38 (53) 
 Male 37 (47) 33 (47) 
B symptoms 44/78 (56) 40/71 (56) 
Ann Arbor stage   
 I-II 5 (6) 5 (7) 
 III-IV 73 (94) 66 (93) 
Number of extranodal sites   
 0-1 40 (51) 38 (53) 
 >1 38 (49) 33 (47) 
ECOG performance status   
 0-1 61 (78) 54 (76) 
 2 17 (22) 17 (24) 
Bone marrow involvement 36/73 (49) 32/66 (48) 
Hypergammaglobulinemia 30/70 (43) 29/64 (45) 
Elevated LDH 42/77 (55) 39/70 (56) 
Histology   
 AITL 67 (94) 67 (86) 
 Nodal PTCL with TFH phenotype 4 (6) 4 (5) 
 Other* 7 (9) 0 (0) 
IPI   
 1-3 48 (62) 43 (61) 
 4-5 29 (38) 27 (39) 
PIT   
 0-2 50 (69) 45 (69) 
 3-4 22 (31) 20 (31) 
SUVmax median (IQR) 11 (7-18) 12 (7-18) 
TMTV median (IQR) 433 (127-937) 468 (125-942) 

Data n (%) or n/N (%) except as noted.

IPI, International Prognostic Index43 ; PIT, Prognostic Index for peripheral T-cell lymphoma, unspecified.44 

*Other diagnosis consisted of T cells and histiocyte-rich diffuse large B-cell lymphoma (N = 1), PTCL that cannot be classified (N = 3), uncertain diagnosis of tumor (N=1), and no histologic material available for pathologic review (N = 2).

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