R. Ketter et al., Predictive value of progression-associated chromosomal aberrations for theprognosis of meningiomas: a retrospective study of 198 cases, J NEUROSURG, 95(4), 2001, pp. 601-607
Object. The goal of this study was to determine whether in meningiomas cyto
genetic findings are suitable as a predictive parameter relevant to prognos
is.
Methods. Between 1992 and 1998 at the Department of Neurosurgery, Saarland
University, 198 patients underwent surgery to resect meningiomas. The menin
giomas were investigated cytogenetically and the patients were followed up
for a mean period of 33 months.
On the basis of the cytogenetic findings, the meningiomas were subdivided i
nto four groups: Group 0 meningiomas displayed a normal diploid chromosome
set; Group 1 tumors were found to have monosomy 22 as the sole cytogenetic
aberrations Group 2 tumors were markedly hypodiploid meningiomas with loss
of additional autosomes in addition to monosomy 22; and Group 3 meningiomas
had deletions of the short arm of a chromosome 1, as well as additional ch
romosomal aberrations including loss of one chromosome 22.
One hundred ninety-eight patients in whom tumor resections were determined
to be Simpson Grade I or II could be followed up after complete tumor extir
pation. In 20 patients, one or several recurrences were documented during t
he period of observation. The tumors were classified according to their dif
ferent, but mostly uniform chromosomal aberrations. Recurrences were found
in six (4.3%) of 139 tumors in Groups 0 and 1 and in two (10.5%) of 19 tumo
rs in Group 2, the highest rate of recurrence was found in 12 (30%,) of 40
tumors in Group 3. This supports the notion that the deletion of the short
arm of one chromosome 1 is an important prognostic factor in meningiomas. T
he results of this study document a significant correlation between histolo
gical grade (p < 0.0001), location (p < 0.0001), and recurrences of meningi
omas (p < 0.0001) (significance determined using chi-square tests).
Conclusions. The cytogenetic classification of meningiomas provides a signi
ficant contribution to the predictability of tumor recurrence and is, there
fore, a valuable criterion for the neurosurgeon's postoperative management
protocol.