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. 2011 Mar 4;104(3):811–815. doi: 10.1007/s11060-011-0551-3

Table 1.

Clinical characteristics of patients with oligodendroglial tumors that developed leptomeningeal disease compared with 196 that did not

  Total Population (n = 204) LMD (n = 8)a No LMD (n = 196)b Significance (p)a vs. b
Mean age in years (range) 42 (18–78) 40 (28–50) 42 (18–78) 0.636
Median KPS (range) 85 (50–100) 85 (70–90) 90 (50–100) 0.477
Debulking (%) 173 (85) 7 (87.5) 166 (85) 0.828
Pathology at diagnosis (%) 0.079
• Oligo. Gr. II 62 (30.5) 1 (12.5) 61 (31.1)
• Oligo. Gr. III 49 (24) 5 (62.5) 44 (22.4)
• Mixed OA Gr. II 52 (25.5) 1 (12.5) 51 (26)
• Mixed OA Gr. III 41 (20) 1 (12.5) 40 (20.4)
1p/19q 0.127
• Not tested (%) 43 (21) 1/7 (14) 42 (21)
• Codeletedc (% of tested) 93/161 (58) 6/7 (86) 87/154 (56.4)
Initial treatment (%) 0.785
• Observation 96 (47) 5 (62.5) 91 (46)
• RT alone 35 (17) 1 (12.5) 34 (17.3)
• ChT alone 18 (9) 1 (12.5) 17 (9)
• SeqRTChT 26 (13) 0 26 (13.3)
• ConcRTChT 29 (14) 1 (12.5) 28 (14.3)
Mean number of recurrences 1.35 2.88 1.27 0.001
PFS (months) (mean; 95% CI) 67 (59–75) 47 (22–72) 68 (59–77) 0.176
OS (months) (mean; 95% CI) 130 (118–142) 107 (82–132) 133 (120–146) 0.063

LMD leptomeningeal disease, Oligo oligodendroglioma, OA oligoastrocytoma, RT radiotherapy, ChT chemotherapy, SeqRTChT sequential RT followed by ChT, ConcRTChT concurrent RT and ChT, PFS progression free survival, OS overall Survival

aPatients with leptomeningeal disease

bPatients without leptomeningeal disease

cIncludes patients with only 1p loss