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. 2010 Dec 22;13(2):223–234. doi: 10.1093/neuonc/noq178

Table 1.

Demographic and treatment characteristics

Total cohort (N = 361)
Five-year survivors (N = 240)
n % n %
Age at diagnosis
 0–4 122 33.8 82 34.2
 5–9 118 32.7 80 33.3
 10–20 121 33.5 78 32.5
Gender
 Male 196 54.3 137 57.1
 Female 165 45.7 103 43.9
Race/ethnicity
 Non-Hispanic, white 281 77.8 194 80.8
 Non-Hispanic, black 69 19.1 41 17.1
 Hispanic 5 1.4 2 0.8
 Other 6 1.7 3 1.3
Tumor location
 Diencephalon 147 40.7 97 40.4
  Hypothalamus/chiasmatic 101 28.0 76 31.7
  Thalamic 43 11.9 20 8.3
  Other 3 0.8 1 0.4
 Cerebellum 94 26.0 61 25.4
 Cerebral hemisphere 56 15.5 38 15.8
  Frontal lobe 15 4.2 10 4.1
  Temporal lobe 28 7.8 20 8.3
  Parietal lobe 7 1.9 4 1.7
  Occipital lobe 2 0.6 2 0.8
  Other 4 1.1 2 0.8
 Brainstem/spinal cord 64 17.7 44 18.3
Extent of resection of primary surgery
 <Gross total 195 54.0 121 50.4
 Gross total 117 32.4 81 33.8
 No surgery 49 13.6 38 15.8
Extent of resection of any surgery
 <Gross total 190 52.6 114 47.5
 Gross total 145 40.2 105 43.8
 No surgery 26 7.2 21 8.8
Primary treatment type
 Surgery only 211 58.5 145 60.4
 Surgery + RT 57 15.8 38 15.8
 Surgery + chemo 34 9.4 14 5.8
 Surgery + RT + chemo 10 2.8 5 2.1
 No Surgery 49 13.6 38 15.8
  No surgery, chemo, or RT 35 9.7 29 12.0
  Chemo only 9 2.5 6 2.5
  RT only 4 1.1 3 1.2
  Chemo + RT 1 0.3 0 0.0
Any treatment type
 Surgery only 165 45.7 110 45.8
 Surgery + RT 83 23.0 67 27.9
 Surgery + RT + chemo 56 15.5 31 12.9
 Surgery + chemo 31 8.6 11 4.6
 No surgery 26 7.2 21 8.8
  No surgery, chemo, or RT 5 1.4 4 1.7
  Chemo only 8 2.2 4 1.7
  RT only 6 1.7 6 2.5
  Chemo + RT 7 1.9 7 2.9
Histology
 Astrocytoma, pilocytic 229 63.4 157 65.4
 Astrocytic tumor, NOS 34 9.4 18 7.5
 Astrocytoma, fibrillary 33 9.1 15 6.3
 Oligodendroglioma 29 8.0 22 9.2
 Glioma, optic 27 7.5 23 9.6
 Astrocytoma, pylomyxoid 5 1.4 3 1.3
 Oligoastrocytoma 4 1.1 2 0.8
Treatment era
 1985–1996 169 46.8 124 51.7
 1997–2007 192 53.2 116 48.3
Vital status
 Alive 317 87.8 230 95.8
 Dead 44 12.2 10 4.2
Progression status
 Never progressed 223 61.8 146 60.8
 Single progression (only) 75 20.8 48 20.0
 Multiple progression 63 17.5 46 19.2
Neurofibromatosis type 1
 No 325 90.0 212 88.3
 Yes 36 10.0 28 11.6

RT, radiation therapy ; NOS, not otherwise specified.