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进展相关染色体畸变对脑膜瘤预后的预测价值:198例回顾性研究

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

作者信息

Ketter R, Henn W, Niedermayer I, Steilen-Gimbel H, König J, Zang K D, Steudel W I

机构信息

Department of Neurosurgery, Institute of Human Genetics, Saarland University, Homburg/Saar, Germany.

出版信息

J Neurosurg. 2001 Oct;95(4):601-7. doi: 10.3171/jns.2001.95.4.0601.

Abstract

OBJECT

The goal of this study was to determine whether in meningiomas cytogenetic findings are suitable as a predictive parameter relevant to prognosis.

METHODS

Between 1992 and 1998 at the Department of Neurosurgery, Saarland University, 198 patients underwent surgery to resect meningiomas. The meningiomas 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 into four groups: Group 0 meningiomas displayed a normal diploid chromosome set; Group 1 tumors were found to have monosomy 22 as the sole cytogenetic aberration; 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 chromosomal 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 extirpation. In 20 patients, one or several recurrences were documented during the period of observation. The tumors were classified according to their different, 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 tumors 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. The results of this study document a significant correlation between histological grade (p < 0.0001), location (p < 0.0001), and recurrences of meningiomas (p < 0.0001) (significance determined using chi-square tests).

CONCLUSIONS

The cytogenetic classification of meningiomas provides a significant contribution to the predictability of tumor recurrence and is, therefore, a valuable criterion for the neurosurgeon's postoperative management protocol.

摘要

目的

本研究的目的是确定在脑膜瘤中,细胞遗传学结果是否适合作为与预后相关的预测参数。

方法

1992年至1998年期间,在萨尔兰大学神经外科,198例患者接受了脑膜瘤切除术。对脑膜瘤进行了细胞遗传学研究,并对患者进行了平均33个月的随访。根据细胞遗传学结果,将脑膜瘤分为四组:0组脑膜瘤显示正常二倍体染色体组;1组肿瘤被发现有22号染色体单体作为唯一的细胞遗传学异常;2组肿瘤是明显的亚二倍体脑膜瘤,除了22号染色体单体之外还存在其他常染色体的缺失;3组脑膜瘤有1号染色体短臂缺失,以及包括一条22号染色体缺失在内的其他染色体异常。198例肿瘤切除被判定为辛普森一级或二级的患者在肿瘤完全切除后可进行随访。在20例患者中,观察期间记录到一次或多次复发。肿瘤根据其不同但大多一致的染色体异常进行分类。0组和1组的139例肿瘤中有6例(4.3%)复发,2组的19例肿瘤中有2例(10.5%)复发;3组的40例肿瘤中有12例(30%)复发率最高。这支持了1号染色体短臂缺失是脑膜瘤重要预后因素的观点。本研究结果表明组织学分级(p<0.0001)、位置(p<0.0001)与脑膜瘤复发(p<0.0001)之间存在显著相关性(使用卡方检验确定显著性)。

结论

脑膜瘤的细胞遗传学分类对肿瘤复发的可预测性有重要贡献,因此是神经外科医生术后管理方案的一个有价值的标准。

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