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dc.contributor.authorLarranaga, Nerea
dc.contributor.authorJose Sanchez, Ma
dc.contributor.authorArdanaz, Eva
dc.contributor.authorFelipe, Saray
dc.contributor.authorMarcos-Gragera, Rafael
dc.contributor.authorRamos Monserrat, Maria
dc.contributor.authorCarulla, Maria
dc.contributor.authorChirlaque, Maria-Dolores
dc.contributor.authorArgueelles, Marcial V
dc.contributor.authorMartos, Carmen
dc.contributor.authorMateo, Antonio
dc.contributor.authorPeris-Bonet, Rafael
dc.date.accessioned2024-07-09T09:13:01Z
dc.date.available2024-07-09T09:13:01Z
dc.date.issued2016
dc.identifier.citationLarranaga N, Sanchez MJ, Ardanaz E, Felipe S, Marcos-Gragera R, Ramos Monserrat M, et al. 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. J Cancer. 2016;7(3):335-43.en
dc.identifier.issn1837-9664
dc.identifier.otherhttp://hdl.handle.net/20.500.13003/17183
dc.identifier.urihttp://hdl.handle.net/20.500.12105/20237
dc.description.abstractObjective: 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.en
dc.language.isoengen
dc.publisherIvyspring International Publisher en
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subjectCancer
dc.subjectSolid tumour
dc.subjectChildhood
dc.subjectAdolescents
dc.subjectPopulation-based study
dc.subjectIncidence
dc.subjectSpain
dc.titleIncidence Patterns and Trends of non-Central Nervous System Solid Tumours in Children and Adolescents. A Collaborative Study of the Spanish Population Based Cancer Registriesen
dc.typeresearch articleen
dc.rights.licenseAttribution-NonCommercial 4.0 International*
dc.identifier.pubmedID26918047es_ES
dc.format.volume7es_ES
dc.format.number3es_ES
dc.format.page335-343es_ES
dc.identifier.doi10.7150/jca.12943
dc.relation.publisherversionhttps://dx.doi.org/10.7150/jca.12943en
dc.identifier.journalJournal of Canceres_ES
dc.rights.accessRightsopen accessen
dc.identifier.scopus2-s2.0-84971577855
dc.identifier.wos370178400014
dc.identifier.puiL610558667


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