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Incidence Patterns and Trends of non-Central Nervous System Solid Tumours in Children and Adolescents. A Collaborative Study of the Spanish Population Based Cancer Registries

机译:儿童和青少年非中央神经系统实体瘤的发病模式和趋势。基于西班牙人口的癌症注册机构的合作研究

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Objective: To describe incidence patterns and trends in children (0-14 years) and adolescents (15-19 age-range) with solid tumours, except those of central nervous system (CNS), in Spain. Methods: Cases were drawn from eleven Spanish population-based cancer registries. Incidence was estimated for the period 1983-2007 and trends were evaluated using Joinpoint regression analysis. Results: The studied tumour groups accounted for 36% of total childhood cancers and 47.6% of those diagnosed in adolescence with annual rates per million of 53.5 and 89.3 respectively. In children 0 to 14 years of age, Neuroblastoma (NB) was the commonest (7.8%) followed by Soft-tissue sarcomas (STS) (6.3%), bone tumours (BT) (6.2%) and renal tumours (RT) (4.5%). NB was the most frequently diagnosed tumour before the 5th birthday, while STS and BT were the commonest at 5-9 years of age, and BT and Carcinoma and other epithelial tumours (COET) at 10-14. COET presented the highest incidence in adolescents, followed by germ-cell tumours (GCT), BT and STS. These four diagnostic groups accounted for 94% of total non-CNS solid tumours, in adolescents. Overall incidence rates increased significantly in children up to 1996 with an annual percentage change (APC) of 2.6% (95%CI: 1.7; 3.6). NB and COET showed significant time trend (APCs: 1.4% and 3.8% respectively) while other tumour groups such as RT, STS, BT or GCT had no significant changes over time. A significant increase was present in NB under the age of 5 and in BT and STS in children aged 10-14 years. In adolescents there were significant increases for all tumours combined (APC=2.7; 95%CI: 1.8-3.6) and for STS, GCT and COET (APCs: 3.2%, 4.4% and 3.5% respectively), while other tumour groups such as hepatic tumours, BT or thyroid carcinomas showed a decreasing trend or no increase. Conclusions: Overall, the incidence of the studied cancers in children increased along the period 1983-1996 with no posterior significant rise, while the incidence in adolescents increased significantly over the whole period 1983-2007. Several specific tumour groups showed significant rises or decrements in childhood or adolescence, although the small number of cases precludes showing significant trends or inflexion points.
机译:目的:描述西班牙(中枢神经系统(CNS)除外)有实体瘤的儿童(0-14岁)和青少年(15-19岁年龄段)的发病模式和趋势。方法:病例来自11个西班牙基于人群的癌症登记处。估计1983-2007年期间的发病率,并使用Joinpoint回归分析评估趋势。结果:所研究的肿瘤组分别占儿童总癌症的36%和青春期诊断的癌症的47.6%,每百万的年发病率分别为53.5和89.3。在0至14岁的儿童中,神经母细胞瘤(NB)是最常见的(7.8%),其次是软组织肉瘤(STS)(6.3%),骨肿瘤(BT)(6.2%)和肾肿瘤(RT)( 4.5%)。 NB是5岁生日之前被诊断最频繁的肿瘤,而STS和BT在5-9岁时最常见,而BT和癌及其他上皮肿瘤(COET)在10-14岁时最为常见。 COET在青少年中发病率最高,其次是生殖细胞肿瘤(GCT),BT和STS。这四个诊断组占青少年非CNS实体瘤总数的94%。截止到1996年,儿童的总发病率显着增加,年百分比变化(APC)为2.6%(95%CI:1.7; 3.6)。 NB和COET表现出显着的时间趋势(APC:分别为1.4%和3.8%),而其他肿瘤组(例如RT,STS,BT或GCT)则不会随时间变化。 5-14岁以下的NB和10-14岁儿童的BT和STS显着增加。在青少年中,所有合并肿瘤(APC = 2.7; 95%CI:1.8-3.6)以及STS,GCT和COET(APC:分别为3.2%,4.4%和3.5%)显着增加,而其他肿瘤组例如肝肿瘤,BT或甲状腺癌呈下降趋势或没有上升。结论:总体而言,研究的儿童癌症发病率在1983-1996年期间有所增加,但没有明显的上升趋势,而在整个1983-2007年期间,青少年的发病率显着增加。几个特定的​​肿瘤组在儿童或青春期表现出明显的上升或下降,尽管少数病例排除了显示明显的趋势或拐点。

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