Table 1.
Development (BCH, n = 214) | External Validation (CBTN, n = 112) | p-values | |
---|---|---|---|
Age (years) | 0.19* | ||
median (range) | 5 (1 – 20) | 6 (1 – 21) | |
Sex n (%) | 0.82+ | ||
Female | 95 (44.4%) | 51 (45.5%) | |
Male | 113 (52.8%) | 55 (49.1%) | |
Unknown | 6 (2.8%) | 4 (3.6%) | |
Race/Ethnicity n (%) | 1.076e-06+ | ||
Non-Hispanic Caucasian/white | 145 (67.8%) | 71 (64.5%) | |
African American/Black | 6 (2.8%) | 14 (12.7%) | |
Hispanic/Latinx | 3 (1.4%) | 10 (9.1%) | |
Asian American/Asian | 9 (4.2%) | 3 (2.7%) | |
American Indian/Alaska Native | 0 | 1 (0.9%) | |
More than once race | 0 | 1 (0.9%) | |
Other/Unknown | 51 (23.8%) | 10 (9.1%) | |
Histologic diagnosis n (%) | 0.0005+ | ||
Pilocytic Astrocytoma | 52 (24.2%) | 68 (61.8%) | |
Fibrillary Astrocytoma | 0 | 8 (7.3%) | |
Pilomyxoid Astrocytoma | 8 (3.7%) | 17 (15.5%) | |
Ganglioglioma | 13 (6.1%) | 0 | |
Dysembryoplastic neuroepithelial tumor | 7 (3.3%) | 0 | |
Diffuse Astrocytoma | 1 (0.5%) | 7 (6.4%) | |
Angiocentric Glioma | 1 (0.5%) | 1 (0.9%) | |
Other Low-Grade Glioma/Astrocytoma | 132 (61.7%) | 9 (8.2%) | |
BRAF Mutation Status n (%) | 0.0005+ | ||
V600E | 50 (23.4%) | 17 (15.2%) | |
Fusion | 60 (28.0%) | 60 (53.6%) | |
Wildtype | 104 (48.6%) | 35 (31.3%) | |
Tumor Locations n (%) | 0.0005+ | ||
Cerebellum/Posterior fossa | 40 (18.7%) | 33 (29.4%) | |
Temporal lobe | 43 (20.1%) | 12 (10.7%) | |
Frontal Lobe | 22 (10.3%) | 4 (3.6%) | |
Suprasellar | 6 (2.8%) | 32 (28.6%) | |
Optic Pathway | 8 (3.7%) | 17 (14.9%) | |
Brainstem | 7 (3.3%) | 9 (7.9%) | |
Thalamus | 15 (7.0%) | 2 (1.8%) | |
Ventricles | 14 (6.5%) | 2 (11.4%) | |
Others | 59 (27.6%) | 1 (0.9%) |
CBTN: Children Brain Tumor Network. The Kruskal-Wallis rank sum test (*) was performed for numerical data age to test the statistical significance between age medians. The Fisher’s Exact test (+) was performed for categorical data to test the statistical significance differences between CBTN and BCH datasets. A p-value less than 0.05 is statistically significant.