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. 2013 Nov 26;16(1):123–130. doi: 10.1093/neuonc/not142

Table 1.

Patient and treatment characteristics

Variable Without 1p/19q Codeletions (n = 51) With 1p/19q Codeletions (n = 37) P
Age, y, at the time of radiotherapy
 20–39 30 (58%) 11 (30%) .020
 40–49 13 (25%) 13 (35%)
 50+ 8 (16%) 13 (35%)
Gender
 Male 27 (53%) 25 (68%) .19
 Female 24 (47%) 12 (32%)
WHO grade
 II 18 (35%) 10 (27%) .49
 III 33 (65%) 27 (73%)
Tumor volume at diagnosis
 Range (cm3)a 5–212 5–163 .46
 Median (cm3)a 48 28
Resection
 Gross total resection 26 (51%) 20 (54%) .77
 Partial resection 19 (37%) 12 (32%)
 Biopsy 6 (12%) 4 (11%)
 AutoLITTb 0 1 (3%)
T2 abnormality at time of adjuvant therapy
 Range (cm3)c 0–146 0–40 .48
 Median (cm3)c 16 9
Location
 Frontal lobe 35 (69%) 33 (89%) .038
 Not frontal lobe 16 (31%) 4 (11%)
p53
 p53 overexpression 28/34 (82%) 4/16 (25%) .00027
 Normal p53 expression 6/34 (18%) 12/16 (75%)
Radiation
 Range (cGy)d 5400–6134 5000–6300 .48
 Median (cGy)d 5940 5940
Chemotherapy
 Concurrent chemotherapy 42 (82%): 40 with temozolomide, 2 with hydroxyurea 32 (86%): 31 with temozolomide, 1 with hydroxyurea .29
 Radiation followed by chemotherapy 6e (12%): 5 with temozolomide, 1 with PCV 1 (3%): 1 with temozolomide
 Radiation alone 3 (6%) 4 (11%)

aData on tumor volume prior to resection were available for 41/51 tumors without 1p/19q codeletions and 33/37 tumors with 1p/19q codeletions.

bAutoLITT is a trademark of Monteris Medical, Plymouth, MN, and is an FDA-approved system that is used to thermally ablate brain tumors via a fiber-optic laser probe.

cData on T2 abnormality at the time of adjuvant therapy were available for 42/51 tumors without 1p/19q codeletions and 30/37 tumors with 1p/19q codeletions.

dData on dose administered were available for 39/51 tumors without 1p/19q codeletions and 33/37 tumors with 1p/19q codeletions.

eIn 1 of these 6 cases, it is unclear whether temozolomide was started before or after completion of radiotherapy. cGy, centigray; PCV, procarbazine, lomustine, and vincristine.