Skip to main content
. Author manuscript; available in PMC: 2011 Jun 21.
Published in final edited form as: J Proteome Res. 2010 May 7;9(5):2610–2618. doi: 10.1021/pr100054v

Table 1.

Clinical characteristicsa

PT Age Sex 1p19q deletion Comment Path % Mib-1 Loc SX Recc C+ Pminost-op XRT TTP (mos) Alive (Y/N) Length F/U (mos) Status at last F/U
1D 47 F + 19q-relative deletion O–II 0.2 R-Fr SZ N NO STR none Y 45 S
2D 48 M + O–II 1.2 L-Fr SZ N YESc GTR none Y 56 S
3D 37 M + O–II 0.9 R-Fr SZ N NO GTR none Y 45 S
4D 29 F + O–II 0 L-Fr SZ N YESc GTR none Y 67 S
5D 29 M + O–II 0.5 R-Fr P Y NO GTR none Y 34 P
1UD 65 M O–II 0 L-T SZ N NO GTR LTF/U NA NA NA
2UD 34 M 19 polysomy O–II NA R-Fr HA N NO GTR LTF/U NA NA NA
3UD 46 F 19qpolysomy O–II 1 L-Fr SZ N NO STR none Y 29 S
4UD 34 M O–II 0b R-Fr SZ N NO STR 7 Y 9 P
5UD 28 F 1, 19polysomy O–II 0.3 L-Fr SZ N NO STR none
a

A: alive, C+: contrast enhancement, CTX: chemotherapy, D: deleted, EOR: extent of resection, Fr: frontal, FU: follow up, GTR: Gross total resection, HA: headache, LT F/U: lost to follow-up, NA: no data, OII: oligodendroglioma grade II, P: progression, path: pathology, recc: recurrence, S: stable, STR: subtotal resection, surv: survival, SX: symptoms, SZ: seizure, T: temporal, TTP: time to progression, UD: undeleted, XRT: irradiation.

b

Focal Mib-1 25%.

c

Minimal.