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Wilms tumour surveillance in at-risk children: Literature review and recommendations from the SIOP-Europe Host Genome Working Group and SIOP Renal Tumour Study Group.

cam.depositDate2021-12-16
cam.issuedOnline2021-06-13
dc.contributor.authorHol, Janna A
dc.contributor.authorJewell, Rosalyn
dc.contributor.authorChowdhury, Tanzina
dc.contributor.authorDuncan, Catriona
dc.contributor.authorNakata, Kayo
dc.contributor.authorOue, Takaharu
dc.contributor.authorGauthier-Villars, Marion
dc.contributor.authorLittooij, Annemieke S
dc.contributor.authorKaneko, Yasuhiko
dc.contributor.authorGraf, Norbert
dc.contributor.authorBourdeaut, Franck
dc.contributor.authorvan den Heuvel-Eibrink, Marry M
dc.contributor.authorPritchard-Jones, Kathy
dc.contributor.authorMaher, Eamonn R
dc.contributor.authorKratz, Christian P
dc.contributor.authorJongmans, Marjolijn CJ
dc.contributor.orcidMaher, Eamonn [0000-0002-6226-6918]
dc.date.accessioned2021-12-18T00:30:39Z
dc.date.available2021-12-18T00:30:39Z
dc.date.issued2021-08
dc.date.updated2021-12-16T15:46:38Z
dc.description.abstractSince previous consensus-based Wilms tumour (WT) surveillance guidelines were published, novel genes and syndromes associated with WT risk have been identified, and diagnostic molecular tests for previously known syndromes have improved. In view of this, the International Society of Pediatric Oncology (SIOP)-Europe Host Genome Working Group and SIOP Renal Tumour Study Group hereby present updated WT surveillance guidelines after an extensive literature review and international consensus meetings. These guidelines are for use by clinical geneticists, pediatricians, pediatric oncologists and radiologists involved in the care of children at risk of WT. Additionally, we emphasise the need to register all patients with a cancer predisposition syndrome in national or international databases, to enable the development of better tumour risk estimates and tumour surveillance programs in the future.
dc.format.mediumPrint-Electronic
dc.identifier.doi10.17863/CAM.79056
dc.identifier.eissn1879-0852
dc.identifier.issn0959-8049
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/331604
dc.language.isoeng
dc.publisherElsevier BV
dc.publisher.departmentDepartment of Medical Genetics
dc.publisher.urlhttp://dx.doi.org/10.1016/j.ejca.2021.05.014
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectCancer predisposition syndrome
dc.subjectNephroblastoma
dc.subjectOvergrowth syndrome
dc.subjectSurveillance
dc.subjectWT1
dc.subjectWilms tumour
dc.subjectEurope
dc.subjectGenomics
dc.subjectHumans
dc.subjectWilms Tumor
dc.titleWilms tumour surveillance in at-risk children: Literature review and recommendations from the SIOP-Europe Host Genome Working Group and SIOP Renal Tumour Study Group.
dc.typeArticle
dcterms.dateAccepted2021-05-07
prism.endingPage63
prism.publicationDate2021
prism.publicationNameEur J Cancer
prism.startingPage51
prism.volume153
pubs.licence-display-nameApollo Repository Deposit Licence Agreement
pubs.licence-identifierapollo-deposit-licence-2-1
rioxxterms.typeJournal Article/Review
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1016/j.ejca.2021.05.014

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