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Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93-01, 2001 and UK-IMPORT database: A report of the SIOP-Renal Tumor Study Group.

dc.contributor.authorvan der Beek, Justine N
dc.contributor.authorHol, Janna A
dc.contributor.authorCoulomb-l'Hermine, Aurore
dc.contributor.authorGraf, Norbert
dc.contributor.authorvan Tinteren, Harm
dc.contributor.authorPritchard-Jones, Kathy
dc.contributor.authorHouwing, Maite E
dc.contributor.authorde Krijger, Ronald R
dc.contributor.authorVujanic, Gordan M
dc.contributor.authorDzhuma, Kristina
dc.contributor.authorSchenk, Jens-Peter
dc.contributor.authorLittooij, Annemieke S
dc.contributor.authorRamírez-Villar, Gema L
dc.contributor.authorMurphy, Dermot
dc.contributor.authorRay, Satyajit
dc.contributor.authorAl-Saadi, Reem
dc.contributor.authorGessler, Manfred
dc.contributor.authorGodzinski, Jan
dc.contributor.authorRuebe, Christian
dc.contributor.authorCollini, Paola
dc.contributor.authorVerschuur, Arnaud C
dc.contributor.authorFrisk, Tony
dc.contributor.authorVokuhl, Christian
dc.contributor.authorHulsbergen-van de Kaa, Christina A
dc.contributor.authorde Camargo, Beatriz
dc.contributor.authorSandstedt, Bengt
dc.contributor.authorSelle, Barbara
dc.contributor.authorTytgat, Godelieve A M
dc.contributor.authorvan den Heuvel-Eibrink, Marry M
dc.date.accessioned2023-02-09T10:39:48Z
dc.date.available2023-02-09T10:39:48Z
dc.date.issued2021-02-03
dc.description.abstractIn children, renal cell carcinoma (RCC) is rare. This study is the first report of pediatric patients with RCC registered by the International Society of Pediatric Oncology-Renal Tumor Study Group (SIOP-RTSG). Pediatric patients with histologically confirmed RCC, registered in SIOP 93-01, 2001 and UK-IMPORT databases, were included. Event-free survival (EFS) and overall survival (OS) were analyzed using the Kaplan-Meier method. Between 1993 and 2019, 122 pediatric patients with RCC were registered. Available detailed data (n = 111) revealed 56 localized, 30 regionally advanced, 25 metastatic and no bilateral cases. Histological classification according to World Health Organization 2004, including immunohistochemical and molecular testing for transcription factor E3 (TFE3) and/or EB (TFEB) translocation, was available for 65/122 patients. In this group, the most common histological subtypes were translocation type RCC (MiT-RCC) (36/64, 56.3%), papillary type (19/64, 29.7%) and clear cell type (4/64, 6.3%). One histological subtype was not reported. In the remaining 57 patients, translocation testing could not be performed, or TFE-cytogenetics and/or immunohistochemistry results were missing. In this group, the most common RCC histological subtypes were papillary type (21/47, 44.7%) and clear cell type (11/47, 23.4%). Ten histological subtypes were not reported. Estimated 5-year (5y) EFS and 5y OS of the total group was 70.5% (95% CI = 61.7%-80.6%) and 84.5% (95% CI = 77.5%-92.2%), respectively. Estimated 5y OS for localized, regionally advanced, and metastatic disease was 96.8%, 92.3%, and 45.6%, respectively. In conclusion, the registered pediatric patients with RCC showed a reasonable outcome. Survival was substantially lower for patients with metastatic disease. This descriptive study stresses the importance of full, prospective registration including TFE-testing.
dc.identifier.doi10.1002/ijc.33476
dc.identifier.essn1097-0215
dc.identifier.pmcPMC8048605
dc.identifier.pmid33460450
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048605/pdf
dc.identifier.unpaywallURLhttps://discovery.ucl.ac.uk/10123469/1/ijc.33476.pdf
dc.identifier.urihttp://hdl.handle.net/10668/16987
dc.issue.number11
dc.journal.titleInternational journal of cancer
dc.journal.titleabbreviationInt J Cancer
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number2724-2735
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectpediatric
dc.subjectrenal cell carcinoma
dc.subjectsurvival
dc.subjecttreatment
dc.subject.meshAdolescent
dc.subject.meshBasic Helix-Loop-Helix Leucine Zipper Transcription Factors
dc.subject.meshCarcinoma, Renal Cell
dc.subject.meshChild
dc.subject.meshChild, Preschool
dc.subject.meshClinical Trials as Topic
dc.subject.meshDatabases, Factual
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshInfant
dc.subject.meshInfant, Newborn
dc.subject.meshKaplan-Meier Estimate
dc.subject.meshKidney Neoplasms
dc.subject.meshMale
dc.subject.meshPrognosis
dc.subject.meshProspective Studies
dc.subject.meshSurvival Analysis
dc.subject.meshTranslocation, Genetic
dc.subject.meshUnited Kingdom
dc.titleCharacteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93-01, 2001 and UK-IMPORT database: A report of the SIOP-Renal Tumor Study Group.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number148
dspace.entity.typePublication

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