Predictive value of progression-associated chromosomal aberrations for theprognosis of meningiomas: a retrospective study of 198 cases

Citation
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
Citations number
51
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROSURGERY
ISSN journal
00223085 → ACNP
Volume
95
Issue
4
Year of publication
2001
Pages
601 - 607
Database
ISI
SICI code
0022-3085(200110)95:4<601:PVOPCA>2.0.ZU;2-7
Abstract
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.