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. 2018 Jul 12;85(2):280–289. doi: 10.1093/neuros/nyy268

TABLE 1.

Clinical and Pathological Characteristics of the NIH Cohort and Distribution of PD-L1 Expression

PD-L1 IHC (SP263) n(%)
Total n = 183a ≥1% n = 54 (29.5) ≥5% n = 43 (23.4) ≥25% n = 28 (15.3)
Age (yr)
 Median (range) 48 (4-75) 52 (4-74) 53 (18-74) 53 (23-74)
Sex
 Female 57 (31) 16 (30) 14 (33) 6 (21)
 Male 124 (69) 38 (70) 29 (67) 22 (79)
Presentation
 Primaryb 46 (25) 13 (24) 11 (26) 9 (3)
 Recurrent/post-therapy 137 (75) 41 (76) 32 (74) 19 (68)
Diagnosis (WHO 2016)
 LGG 6 (3.3) 0 (0) 0 (0) 0 (0)
 AA, IDHmut 21 (11.6) 1 (1.8) 0 (0) 0 (0)
 AO, IDH-mut/1p19q codeleted 5 (2.7) 2 (3.7) 1 (2.3) 1 (3.6)
 Glioblastoma, IDHwt 81 (44.2) 37 (68.5) 30 (69.7) 20 (71.4)
 Glioblastoma, IDHmut 13 (7.1) 2 (3.7) 1 (2.3) 0 (0)
Glioblastoma, NOS 31 (16.9) 12 (22.2) 11 (25.6) 7 (25)
 DMG, H3K27Mmut 16 (8.8) 0 (0) 0 (0) 0 (0)

LGG, low-grade (diffuse) glioma (WHO grade II); AA, anaplastic astrocytoma; AO, anaplastic oligodendroglioma; DMG, diffuse midline glioma.

an = 5 cases did not have available clinical information.

bPrior to chemotherapy or radiotherapy.

Glioblastoma, NOS: WHO grade IV diffuse gliomas with negative IDH R132H staining and an alternative IDH1 or IDH2 mutation probability between 11 and 89%.

Not shown: AANOS (not otherwise specified, n = 2); AAIDHwt (n = 1); AOANOS (anaplastic oligoastrocytoma, n = 1); AONOS (n = 1); DMG non-H3K27M (n = 5).