Table 3.
All adverse outcomes | High‐grade progression/death | ||||
---|---|---|---|---|---|
Variable | RR (95% CI) | P | Variable | RR | P |
IDH1‐mutant | 1.38 (1.05–1.81) | 0.0007 | IDH1‐mutant | 2.89 (0.93–8.96) | 0.0002 |
WHO grade >I | 1.47 (1.07–2.01) | 0.0046 | WHO grade >I | 4.09 (0.71–23.7) | 0.0074 |
Any mitoses | 1.61 (0.92–2.01) | 0.060 | Age ≥20 years | ∞ | 0.0055 |
Non‐temporal | 1.37 (0.80–2.35) | 0.31 | Any mitoses | 1.20 (0.93–1.55) | 0.061 |
Male gender | 1.17 (0.64–2.15) | 0.62 | Male gender | 1.31 (0.41–4.18) | 0.70 |
Age ≥20 years | 1.07 (0.64–1.77) | 1.00 | Non‐temporal | 1.10 (0.48–2.51) | 1.00 |
Outcomes of 86 gangliogliomas were scored for either all adverse outcome or strictly for high‐grade progression/death (see Methods). Variables were ranked according to statistical significance of relative risk (RR; via Fisher's exact test) in correlating with each type of outcome. (∞ = no case under 20 years old showed high‐grade progression or death.) Of note, the World Health Organization (WHO) grade >I group includes all gangliogliomas with “atypical” features as well as grade III anaplastic gangliogliomas (Table 1).