Skip to main content
. 2012 Oct 15;31(3):337–343. doi: 10.1200/JCO.2012.43.2674

Table 1.

Clinical and Molecular Characteristics

Characteristic PCV/RT (n = 148)
RT (n = 143)
No. % No. %
Age, years
    Median 43 43
    Range 18-75 19-76
Age, years*
    < 50 102 69 99 69
    ≥ 50 46 31 44 31
Sex
    Male 90 61 84 59
    Female 58 39 59 41
Neurologic function
    No symptoms 47 32 47 33
    Minor symptoms 73 49 69 48
    Moderate (active) 17 12 12 8
    Moderate (inactive) 11 7 14 10
    Unknown 0 0 1 1
KPS*
    60-70 15 10 15 10
    80-100 133 90 128 90
Surgery
    Total resection 40 27 53 37
    Partial procedure 85 57 75 52
    Biopsy only 21 14 14 10
    No details 2 1 1 1
Tumor type
    AO 77 52 73 51
    AOA (oligodendroglioma dominant) 28 19 37 26
    AOA (neither element dominant) 24 16 15 11
    AOA (astrocytoma dominant) 19 13 18 13
Tumor grade*
    Moderately anaplastic 80 54 81 57
    Highly anaplastic 68 46 62 43
Multifocal tumor
    Yes 15 10 10 7
    No 132 89 131 92
    Unknown 1 1 2 1
Corticosteroids at baseline
    Yes 92 62 79 55
    No 56 38 64 45
Chromosome 1p
    Known 134 128
    1p deleted 66 49 76 59
    1p intact 68 51 52 41
    Unknown 14 15
Chromosome 19q
    Known 135 129
    19q deleted 85 63 82 64
    19q intact 50 37 47 36
    Unknown 13 14
Chromosomes 1p & 19q
    Known 135 128
    Both deleted 59 44 67 52
    One or neither deleted 76 56 61 48
    Unknown 13 15

Abbreviations: AO, anaplastic oligodendroglioma; AOA, anaplastic oligoastrocytoma; KPS, Karnofsky performance status; PCV, procarbazine, lomustine, and vincristine; RT, radiotherapy.

*

Stratification factors at randomization.

No. and % of known.