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. 2020 May 5;9(13):4768–4776. doi: 10.1002/cam4.3104

TABLE 1.

Clinical and phenotypic characteristics of patients with PD‐L1+ and PD‐L1 IVLBCL

Variables PD‐L1+ IVLBCL (n = 12) PD‐L1 IVLBCL (n = 22) P
Sex (male/female) 5/7 11/11 .72
Age, median (range) 74 (51‐81) 75 (64‐86) .036
Age > 60 y 9/12 (75%) 22/22 (100) .037
Performance status > 1 8/12 (75%) 16/21 (76%) .69
IPI (HI/H) 10/11 (91%) 20/21 (95%) 1.0
Stage III/IV 11/12 (92%) 21/21 (100%) .36
plt < 14 × 104/μL 9/11 (82%) 14/21 (67%) .44
WBC < 3.5 × 103/μL 4/11 (36%) 3/21 (14%) .20
Alb < 3.0 g/dL 8/11 (73%) 19/21 (90) .31
CRP > 1.0 mg/dL 11/11 (100%) 20/21 (95%) 1.0
sIL‐2R > normal 11/12 (92%) 21/21 (100%) .36
LDH > normal 11/11 (100%) 20/21 (95%) 1.0
Hb < 11 9/11 (81%) 15/21 (71%) .68
B symptoms 8/12 (67%) 19/22 (86%) .21
Hepatomegaly 1/12 (8.3%) 4/19 (21%) .62
Splenomegaly 7/12 (58%) 8/19 (42%) .47
Respiratory symptoms 1/12 (8.3%) 10/18 (56%) .018
CNS symptoms 6/12 (50%) 8/19 (42%) .72
Cutaneous involvement 9/12 (75%) 16/22 (55%) .61
Variant (Classic/HPS) 2/9 1/20 .27
CD5 positivity 2/7 (29%) 8/19 (42%) .67
COO (GCB/non‐GCB subtype) 1/6 2/15 1.0

P value with siginificant difference are shown in bold value.

Abbreviations: Alb, albumin; CNS, central nervous system; COO, cell of origin; CRP, C‐reactive protein; GCB, germinal center B cell; H, high; Hb, hemoglobin; HI, high‐intermediate; HPS, hemophagocytic syndrome; IPI, international prognostic index; LDH, lactate dehydrogenase; plt, platelet; sIL‐2R, soluble interleukin‐2 receptor; WBC, white blood cell.