Clinicopathologic study of 85 similarly treated patients with anaplastic astrocytic tumors - An analysis of DNA content (ploidy), cellular proliferation, and p53 expression
A. Perry et al., Clinicopathologic study of 85 similarly treated patients with anaplastic astrocytic tumors - An analysis of DNA content (ploidy), cellular proliferation, and p53 expression, CANCER, 86(4), 1999, pp. 672-683
BACKGROUND. The biologic behavior of anaplastic (World Health Organization
Grade III) astrocytomas and oligoastrocytomas is highly variable, ranging f
rom rapid progression to prolonged survival. It is difficult to predict the
outcome of an individual patient based on morphology alone.
METHODS. To determine the prognostic value of commonly used clinicopatholog
ic markers, we reviewed our experience with 85 similarly treated patients e
nrolled in 3 North Central Cancer Treatment Group high grade glioma protoco
ls. The pathology was comprised exclusively of primary anaplastic astrocyti
c tumors (66 astrocytomas and 19 oligoastrocytomas). Variables examined inc
luded patient age, morphologic type, preoperative performance score, extent
of surgery, solitary versus multiple mitoses, DNA flow cytometric and imag
e morphometric parameters, and expression of proliferating cell nuclear ant
igen, MIB-1, and p53 expression.
RESULTS. The study was comprised of 48 men and 37 women ranging in age from
14-79 years (median age, 47 years). Overall survival ranged from <1 month
to >12 years (median, 21.6 months). Statistical analyses revealed that age
accounted for the majority of this extensive variability in survival. The m
edian survival rimes were 65.5 months, 22.1 months, and 4.4 months, respect
ively, for the groups <40 years, 40-59 years, and greater than or equal to
60 years, respectively (P < 0.0001). On univariate analyses, aneuploidy by
flow cytometry and a low performance score also predicted a better survival
(P values of 0.04 and 0.009, respectively). Statistical trends predicting
a better survival were observed for patients with a solitary mitosis and p5
3 immunopositivity. However, only patient age remained significant in multi
variate models.
CONCLUSIONS. In a small but relatively uniformly treated cohort of patients
with anaplastic astrocytomas and oligoastrocytomas, patient age was associ
ated strongly and inversely with overall survival. Once patient age was tak
en into account, the clinical and pathologic markers tested appeared to be
of limited prognostic value. Cancer 1999;86:672-83, (C) 1999 American Cance
r Society.