A COMPARISON OF THE PREDICTIVE POWER FOR SURVIVAL IN GLIOMAS PROVIDEDBY MIB-1, BROMODEOXYURIDINE AND PROLIFERATING CELL NUCLEAR ANTIGEN WITH HISTOPATHOLOGIC AND CLINICAL-PARAMETERS
Pe. Mckeever et al., A COMPARISON OF THE PREDICTIVE POWER FOR SURVIVAL IN GLIOMAS PROVIDEDBY MIB-1, BROMODEOXYURIDINE AND PROLIFERATING CELL NUCLEAR ANTIGEN WITH HISTOPATHOLOGIC AND CLINICAL-PARAMETERS, Journal of neuropathology and experimental neurology, 56(7), 1997, pp. 798-805
The purpose of this prospective study of 65 patients was to compare si
de-by-side the predictive power for survival of (a) MIB-1, (b) bromode
oxyuridine (BUDR), and (c) proliferating cell nuclear antigen (PCNA).
They were compared (a) with each other. (b) with several clinical pred
ictors, and (c) with histopathologic grade under actual clinical biops
y conditions in a study of 1993 World Wealth Organization (WHO) grade
II to IV adult supratentorial gliomas. There was a strong positive rel
ationship between MIB-1 and BUDR by Spearman Rank correlation. In univ
ariate analysis, MIB-1 (logrank p = 0.06) was more predictive of survi
val than BUDR or PCNA. Longer survivors were distinguished from others
by the lowest MIB-1 labeling indices (LI less than or equal to 2.5%)
better than by the lowest histopathologic grade. However, histopatholo
gic grades were highly predictive among the entire group (logrank p <
0.0001). Young age (p < 0.0001) and high Karnofsky performance status
(p < 0.0001) were the clinical factors most predictive of longer survi
val. Female gender correlated with longer survival (logrank p = 0.02).
In multivariate Cox proportional hazards models, age, Karnofsky perfo
rmance status. and histopathologic grading remained statistically sign
ificant after full reduction of the model. We conclude that Ki-67 meas
ured by MIB-1 monoclonal antibody was superior to other markers of pro
liferation. When all factors are considered simultaneously over all 3
grades of malignancy, greatest predictive power resides in histopathol
ogic grade and clinical variables. MLB-1 is expected to be most import
ant in eases where clinical or histopathologic factors are ambiguous o
r where they cannot be fully assessed.