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. 2022 May 12;12:874462. doi: 10.3389/fonc.2022.874462

Table 1.

Characteristics of patients with initial CNS disease (n = 13) and all peripheral T-cell lymphomas (n = 1,040).

Characteristics Initial CNS disease (n = 13 pts) PTCL without initial CNS involvement (n = 1,027 pts)
Subtype of PTCL
PTCL-NOS 10* 406
ALCL ALK neg. 1 157
ALCL ALK pos. 0 74
AITL 1 108
EATL 1 38
MEITL 0 1
Other 0 243
Age, median (range) years 61.0 (24–80) 60.0 (18–92)
Gender, Male/Female 7/6 600/427
Clinical stage
I(E) 2* 165
II(E) 0 183
III(E) 0 246
IV 11 433
ECOG PS
0 3 329
1 3 381
2 3 200
3 2 90
4 2 27
B symptoms, Yes/No
7/6 507/520
Bulky mass ≥10 cm, Yes/No 2/11 107/920
Number of extranodal sites
0–1 3 819
≥2 10 208
LDH ≥ ULN, Yes/No 6/7 627/400
International Prognostic Index
0 0 228
1 2 106
2 1 219
3 4 246
4 4 121
5 2 107
Involved CNS sites
Parenchymal 6*
Leptomeningeal 4
Parenchymal and leptomeningeal 2
Ocular and leptomeningeal 1
Deep brain structures involved
Yes/No 3/10
Cerebrospinal fluid protein concentration elevated
Yes/No/Missing 6/3/4

pts, patients; PTCL, peripheral T-cell lymphoma; NOS, not otherwise specified; ALCL, anaplastic large cell lymphoma; ALK, anaplastic lymphoma kinase; AITL, angioimmunoblastic T-cell lymphoma; EATL, enteropathy-associated T-cell lymphoma; MEITL, monomorphic epitheliotropic intestinal T-cell lymphoma; ECOG PS, the Eastern Cooperative Oncology Group Performance status; LDH, lactate dehydrogenase; ULN, upper limit of normal. *Two patients with primary T CNS lymphoma.