TABLE 1.
n (%) | Range | Mean (SD) | |
---|---|---|---|
Child sex | |||
Male | 32 (44.4) | — | — |
Female | 40 (55.6) | — | — |
Child race | |||
White | 46 (63.9) | — | — |
Black | 11 (15.3) | — | — |
Hispanic | 3 (4.2) | — | — |
Asian | 3 (4.2) | — | — |
Hawaiian | 1 (1.4) | — | — |
Multi-racial | 3 (4.2) | — | — |
Not reported | 3 (4.2) | — | — |
Other | 2 (2.8) | — | — |
Age at diagnosis (y) | — | 0.5-18.5 | 7.7 (5.0) |
Age at evaluation (y) | — | 7.2-21.8 | 13.7 (4.0) |
Time since diagnosis (y) | — | 2.0-16.2 | 6.0 (4.0) |
NPS | — | 0-10 | 4.8 (2.4) |
Tumor Location | |||
Infratentorial | 35 (48.6) | — | — |
Supratentorial | 18 (25.0) | — | — |
Midbrain | 19 (26.4) | — | — |
Lobule* | |||
Frontal | 10 (13.9) | — | — |
Parietal | 2 (2.8) | — | — |
Temporal | 4 (5.6) | — | — |
Occipital | 3 (4.2) | — | — |
Midbrain | 19 (26.4) | — | — |
Cerebellum | 35 (48.6) | — | — |
Pathology | |||
Astrocytoma | 16 (22.2) | — | — |
ATRT | 1 (1.4) | — | — |
Craniopharyngioma | 8 (11.1) | — | — |
Ependymoma | 8 (11.1) | — | — |
Gangliocytoma | 3 (4.2) | — | — |
Glioma | 14 (19.4) | — | — |
Germinoma | 4 (5.6) | — | — |
Central Nervous System Neuroblastoma | 2 (2.8) | — | — |
Medulloblastoma | 8 (11.1) | — | — |
Meningioma | 1 (1.4) | — | — |
Papilloma | 2 (2.8) | — | — |
Pineoblastoma | 2 (2.8) | — | — |
PNET | 3 (4.2) | — | — |
Treatment Completed | |||
Resection | 61 (84.7) | — | — |
Chemotherapy | 38 (52.8) | — | — |
Radiation | 29 (40.3) | — | — |
Value greater than 100% as one participant had multi-lobule involvement.
ATRT indicates Atypical Teratoid Rhabdoid Tumor; NPS, Neurological Predictor Scale score cumulative neuro-oncologic risk score based upon history of hydrocephalus, seizures, endocrinopathies, chemotherapy, extent and number of neuro-surgeries, and type of radiation therapy; PNET, Primitive neuroectodermal tumor.