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. Author manuscript; available in PMC: 2022 Oct 1.
Published in final edited form as: J Neurooncol. 2021 Oct 1;155(1):93–100. doi: 10.1007/s11060-021-03847-y

TABLE 1.

Clinical and demographic characteristics of patients with pediatric medulloblastoma, 1997–2016

XRT
(n=54)
PRT
(n=64)
P-value
Mean age at diagnosis, year (SD) 8.47 (4.04) 6.83 (3.20) 0.02
Sex, n(%) 0.42
 Male 41 (75.9) 44 (68.8)
 Female 13 (24.1) 20 (31.3)
Race/Ethnicity, n(%) 0.37
 Non-Hispanic White 19 (35.2) 29 (45.3)
 Hispanic 19 (35.2) 23 (35.9)
 Non-Hispanic Black 11 (20.4) 6 (9.4)
 Non-Hispanic Other 5 (9.3) 6 (9.4)
CSI radiation dose, n(%)* 0.24
 <30 Gy 40 (74.1) 40 (63.5)
 ≥30 Gy 14 (25.9) 23 (36.5)
Treatment Protocol, n(%)* <0.001
 SJMB 961 22 (40.7) 0 (0.0)
 SJMB 032 15 (27.8) 38 (60.3)
 COG AA99613 14 (25.9) 7 (11.1)
 SJMB 124 0 (0.0) 9 (14.3)
 Other 3 (5.6) 9 (14.3)
Diagnosis Year, n(%) <0.001
 1997–2005 44 (81.5) 0 (0.0)
 2006–2016 10 (18.5) 64 (100.0)

XRT, photon radiation therapy; PRT, proton radiation therapy; SD, standard deviation; CSI, craniospinal irradiation; SJMB, St. Jude Medulloblastoma; COG, Children’s Oncology Group

*

Data incomplete for CSI radiation dose (n=1) and treatment protocol (n=1).

1

Per protocol, treated with 23.4 Gy for average-risk disease and 36.0–39.6 Gy for high-risk disease

2

Per protocol, treated with 23.4 Gy for average-risk disease and 36.0–39.6 Gy for high-risk disease

3

Per protocol, treated with 23.4 Gy CSI and 55.8 Gy total dose to PF

4

Radiation dose dependent upon molecular subtype and further risk stratification related to residual disease, histology, and presence of metastasis