Farinotti M, Ferrarini M, Solari A, Filippini G
Istituto Nazionale Neurologico C. Besta, Sezione di Neuroepidemiologia e Biostatistica, Milan, Italy.
Brain. 1998 Aug;121 ( Pt 8):1429-36. doi: 10.1093/brain/121.8.1429.
Incidence rates for CNS tumours in children of age 0-14 years in the Region of Lombardy, Italy, during the period 1988-93 were analysed; survival probability updated to December 1995 was also estimated. CNS tumours defined according to the International Classification of Diseases for Oncology codes were actively searched for. CNS tumours were diagnosed in 296 children. The age-standardized rates were 40.0 per million child years for both sexes together, and 45.3 for boys and 34.4 for girls. In all age groups, boys had a higher incidence than girls. The annual incidences were 13.7, 7.0, 5.8 for astrocytoma, medulloblastoma and ependymoma, respectively. The overall survival percentages at 5 and 8 years after diagnosis were 68 and 66, respectively. Prognosis was good for astrocytoma (5-year survival, 81%), and declined in the order: other gliomas (5-year survival, 76%); ependymoma (5-year survival, 62%), and medulloblastoma (5-year survival, 43%). The histological type of the tumour was the most powerful independent predictor of survival in children with a CNS tumour. Medulloblastoma/primitive neuroectodermal tumours appeared to have the highest risk of a poor prognosis compared with astrocytoma (relative risk, 3.27; 95% confidence interval, 1.81-5.91). Age at diagnosis and sex had no significant effect on survival. The incidence of childhood CNS tumours found in this study is higher than previously reported in Italy, and is one of the highest in the world from population-based data. Survival of children with brain tumours has improved greatly in recent years. These results suggest that children in Lombardy with CNS tumours had a good survival experience compatible with high quality of care.
对1988 - 1993年期间意大利伦巴第地区0 - 14岁儿童中枢神经系统肿瘤的发病率进行了分析;还估计了截至1995年12月的生存概率。根据国际肿瘤疾病分类编码确定的中枢神经系统肿瘤进行了积极搜索。296名儿童被诊断患有中枢神经系统肿瘤。男女合计的年龄标准化发病率为每百万儿童年40.0例,男孩为45.3例,女孩为34.4例。在所有年龄组中,男孩的发病率高于女孩。星形细胞瘤、髓母细胞瘤和室管膜瘤的年发病率分别为13.7、7.0、5.8。诊断后5年和8年的总体生存率分别为68%和66%。星形细胞瘤的预后良好(5年生存率,81%),其他胶质瘤(5年生存率,76%)、室管膜瘤(5年生存率,62%)和髓母细胞瘤(5年生存率,43%)的预后依次下降。肿瘤的组织学类型是中枢神经系统肿瘤患儿生存的最有力独立预测因素。与星形细胞瘤相比,髓母细胞瘤/原始神经外胚层肿瘤的预后不良风险似乎最高(相对风险,3.27;95%置信区间,1.81 - 5.91)。诊断时的年龄和性别对生存没有显著影响。本研究中发现的儿童中枢神经系统肿瘤发病率高于意大利此前报道的水平,并且从基于人群的数据来看是世界上最高的之一。近年来,脑肿瘤患儿的生存率有了很大提高。这些结果表明,伦巴第地区患有中枢神经系统肿瘤的儿童有良好的生存经历,这与高质量的护理是相符的。