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. 2022 Sep 6;14:17588359221113693. doi: 10.1177/17588359221113693

Table 2.

Molecular characteristics of the DIPG patients’ cohort treated with or without target therapies.

Target therapy No target therapy
Number (%) 9 (36%) 16 (64%)
Histological and IHC findings
Hypercellularity
 Yes, n (%) 5 (55.5) 10 (62.5)
 No, n (%) 4 (44.5) 6 (37.5)
 Data missing, n (%) 0 (0) (0)
Mitoses
 Low, n (%) 4 (44.5) 9 (56)
 High, n (%) 3 (33.5) 4 (25)
 Data missing, n (%) 2 (22) (19)
Atypia
 Mild, n (%) 4 (44.5) 8 (50)
 Moderate, n (%) 4 (44.5) 6 (37.5)
 Severe, n (%) 1 (11) 2 (12.5)
 Data missing, n (%) 0 (0) (0)
Ki67 expression
 ⩽5%, n (%) 3 (33.3) 1 (6.25)
 5–15%, n (%) 3 (33.3) 8 (50)
 >15%, n (%) 2 (22.3) 5 (31.25)
 Data missing, n (%) 1 (11.1) (12.5)
P53 expression
 >50%, n (%) 2 (22) 8 (50)
 <50%, n (%) 5 (56) 5 (31.25)
 Data missing, n (%) 2 (22) (18.75)
ATRX
 Maintained, n (%) 5 (55.6) 9 (56.25)
 Lost, n (%) 2 (22.2) 3 (18.75)
 Data missing, n (%) 2 (22.2) (25)
H3K27 me3
 Maintained, n (%) 1 (11.1) 0 (0)
 Lost, n (%) 8 (88.9) 11 (68.75)
 Data missing, n (%) 0 (0) 5 (31.25)
H3K27M IHC
 Positivity, n (%) 8 (89) 16 (100)
 Negativity, n (%) 1 (11) 0 (0)
 Data missing, n (%) 0 (0) (0)
BRAF IHC
 Expressed, n (%) 1 (11) 0 (0)
 Not expressed, n (%) 4 (44,5) 10 (62.5)
 Data missing, n (%) 4 (44,5) (37.5)
mTOR/pm-TOR IHC
 Expressed, n (%) 7 (78) 3 (19)
 Not expressed, n (%) 0 (0) 4 (25)
 Data missing, n (%) 2 (22) 9 (56)
Molecular findings
 Histone mutation detection 8 (88.9) 16 (100)
Type of mutation
 H3F3A, n (%) 3 (37.5) 11 (68.5)
 HIST1H3B, n (%) 5 (62.5) 4 (25)
 HIST2H3C, n (%) 0 (0) 1 (6.5)
 ACVR1 detection 8 (88.9) 16 (100)
ACVR1 mutated, n (%) 4 (50) 4 (25)
 Wild-type, n (%) 4 (50) 12 (75)

DIPG, diffuse intrinsic pontine glioma; IHC, immunohistochemistry.