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. Author manuscript; available in PMC: 2018 Jun 1.
Published in final edited form as: Acta Neuropathol. 2017 Mar 2;133(6):1001–1016. doi: 10.1007/s00401-017-1690-1

Table 5.

Associations of age at diagnosis, and tumor TERT and ATRX status with overall survival in Group 4: IDH-wildtype glioblastomas.

N (column %) Age Median (range) Percent deceased Median survival years (95% CI) Univariate analysis Multivariate analysisc
Hazard ratio 95% CI p value Hazard ratio 95% CI p value
All/Age (continuous) 309 (100%) 59 (24–89) 81% 1.2 (1.1–1.3) 1.04 (1.02–1.05) <0.0001

TERT-WT 70 (23%) 52 (24–85)a 83% 1.8 (1.2–2.2) 0.67 (0.5–0.91) 0.01 0.90 (0.65–1.25) 0.53
TERT-MUT 239 (77%) 62 (30–89)a 80% 1.1 (1.1–1.2) Ref Ref

ATRX-WT 298 (96%) 60 (24–89)b 81% 1.2 (1.1–1.3) Ref Ref
ATRX-MUT 11 (4%) 38 (33–61)b 64% 4.7 (2-NA) 0.29 (0.14–0.62) 0.001 0.36 (0.17–0.81) 0.01
a

Patients with TERT-mutant tumors were older at diagnosis than patients with TERT-wildtype tumors (p<0.001).

b

Patients with ATRX-mutant tumors were younger at diagnosis than patients with ATRX-wildtype tumors (p<0.001).

c

Multivariate model includes TERT and ATRX status and was stratified by age (grouped as 24–53, 54–70, and 71–89) because age did not meet the Cox model’s proportionality assumptions.

In a model with ATRX alone, stratified by age at diagnosis, ATRX was significantly associated with survival better (hazard ratio: 0.35, 95% CI: 0.16–0.75, p value: 0.007)

Bolded values are statistically significant; 95% CI: 95% confidence interval; Ref: reference group.