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法国儿童实体瘤国家登记处中中枢神经系统原始肿瘤患儿的发病率和生存率。

Incidence and survival of children with central nervous system primitive tumors in the French National Registry of Childhood Solid Tumors.

作者信息

Desandes Emmanuel, Guissou Sandra, Chastagner Pascal, Lacour Brigitte

出版信息

Neuro Oncol. 2014 Jul;16(7):975-83. doi: 10.1093/neuonc/not309.

Abstract

BACKGROUND

Central nervous system (CNS) tumors are the second most common childhood malignancy. The French National Registry of Childhood Solid Tumors (NRCST) makes it possible to describe this variety of distinct tumor types and to provide incidence and survival data in France on a nationwide basis.

METHODS

All children aged 0-14 years, who were registered with a primary CNS tumor in the NRCST of France between 2000 and 2008, were identified. Tumors were classified according to the International Classification of Childhood Cancer, third edition.

RESULTS

Approximately 57% of pediatric CNS tumors were gliomas, with astrocytomas of the pilocytic type predominating. Distributions of subtypes by age showed that primitive neuroectodermal tumors and ependymomas mainly occurred in children aged <5 years. The mean annual incidence rate of CNS tumors was 39 per million. No statistically significant change in time trends of incidence rate was observed during 2000-2008. For all tumors combined, overall survival was 84.8% (95% CI, 83.7%-85.9%) at 1 year and 72.9% (95% CI, 71.5%-74.3%) at 5 years. Survival time trends were studied in a multivariate analysis observing a reduction in the risk of death in periods of diagnosis 2003-2005 (HR = 0.8; 95% CI, 0.7–0.9) and 2006-2008 (HR = 0.7; 95% CI, 0.6-0.9) compared with 2000-2002.

CONCLUSIONS

The stable incidence rates during the last 10 years could indicate that major changes in environmental risk factors are unlikely, but the ongoing need for population-based surveillance remains relevant. Results indicate a positive trend in the survival probability still persistent in the 2000s.

摘要

背景

中枢神经系统(CNS)肿瘤是儿童期第二常见的恶性肿瘤。法国国家儿童实体瘤登记处(NRCST)使得描述这种多样的不同肿瘤类型并在全国范围内提供法国的发病率和生存数据成为可能。

方法

确定了2000年至2008年间在法国NRCST登记患有原发性CNS肿瘤的所有0至14岁儿童。肿瘤根据《国际儿童癌症分类》第三版进行分类。

结果

约57%的儿童CNS肿瘤为胶质瘤,以毛细胞型星形细胞瘤为主。各亚型按年龄分布显示,原始神经外胚层肿瘤和室管膜瘤主要发生在5岁以下儿童。CNS肿瘤的年平均发病率为每百万39例。在2000 - 2008年期间未观察到发病率时间趋势的统计学显著变化。对于所有合并的肿瘤,1年总生存率为84.8%(95%CI,83.7% - 85.9%),5年总生存率为72.9%(95%CI,71.5% - 74.3%)。通过多变量分析研究生存时间趋势,观察到与2000 - 2002年相比,2003 - 2005年诊断期死亡风险降低(HR = 0.8;95%CI,0.7 - 0.9),2006 - 2008年诊断期死亡风险降低(HR = 0.7;95%CI,0.6 - 0.9)。

结论

过去10年发病率稳定可能表明环境危险因素不太可能发生重大变化,但持续进行基于人群的监测仍然很有必要。结果表明21世纪生存率仍呈上升趋势。

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