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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorWatson, Tom A.
dc.contributor.authorNievelstein, Rutger A.J.
dc.contributor.authorBrisse, Hervé J.
dc.contributor.authorLederman, Henrique
dc.contributor.authorComa Muñoz, Ana
dc.contributor.authorvan der Beek, Justine
dc.contributor.authorMorosi, Carlo
dc.date.accessioned2022-07-19T08:58:51Z
dc.date.available2022-07-19T08:58:51Z
dc.date.issued2022-02
dc.identifier.citationvan der Beek JN, Watson TA, Nievelstein RAJ, Brisse HJ, Morosi C, Lederman HM, et al. MRI Characteristics of Pediatric Renal Tumors: A SIOP-RTSG Radiology Panel Delphi Study. J Magn Reson Imaging. 2022 Feb;55(2):543–52.
dc.identifier.issn1522-2586
dc.identifier.urihttps://hdl.handle.net/11351/7811
dc.descriptionWilms tumor; Pediatric; Renal tumor
dc.description.abstractBackground: The SIOP-Renal Tumor Study Group (RTSG) does not advocate invasive procedures to determine histology before the start of therapy. This may induce misdiagnosis-based treatment initiation, but only for a relatively small percentage of approximately 10% of non-Wilms tumors (non-WTs). MRI could be useful for reducing misdiagnosis, but there is no global consensus on differentiating characteristics. Purpose: To identify MRI characteristics that may be used for discrimination of newly diagnosed pediatric renal tumors. Study type: Consensus process using a Delphi method. Population: Not applicable. Field strength/sequence: Abdominal MRI including T1- and T2-weighted imaging, contrast-enhanced MRI, and diffusion-weighted imaging at 1.5 or 3 T. Assessment: Twenty-three radiologists from the SIOP-RTSG radiology panel with ≥5 years of experience in MRI of pediatric renal tumors and/or who had assessed ≥50 MRI scans of pediatric renal tumors in the past 5 years identified potentially discriminatory characteristics in the first questionnaire. These characteristics were scored in the subsequent second round, consisting of 5-point Likert scales, ranking- and multiple choice questions. Statistical tests: The cut-off value for consensus and agreement among the majority was ≥75% and ≥60%, respectively, with a median of ≥4 on the Likert scale. Results: Consensus on specific characteristics mainly concerned the discrimination between WTs and non-WTs, and WTs and nephrogenic rest(s) (NR)/nephroblastomatosis. The presence of bilateral lesions (75.0%) and NR/nephroblastomatosis (65.0%) were MRI characteristics indicated as specific for the diagnosis of a WT, and 91.3% of the participants agreed that MRI is useful to distinguish NR/nephroblastomatosis from WT. Furthermore, all participants agreed that age influenced their prediction in the discrimination of pediatric renal tumors. Data conclusion: Although the discrimination of pediatric renal tumors based on MRI remains challenging, this study identified some specific characteristics for tumor subtypes, based on the shared opinion of experts. These results may guide future validation studies and innovative efforts.
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesJournal of Magnetic Resonance Imaging;55(2)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectRonyons - Malalties - Imatgeria per ressonància magnètica
dc.subjectMedicina clínica - Presa de decisions
dc.subject.meshKidney Neoplasms
dc.subject.mesh/diagnostic imaging
dc.titleMRI Characteristics of Pediatric Renal Tumors: A SIOP-RTSG Radiology Panel Delphi Study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1002/jmri.27878
dc.subject.decsneoplasias renales
dc.subject.decs/diagnóstico por imagen
dc.relation.publishversionhttps://doi.org/10.1002/jmri.27878
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[van der Beek JN, Nievelstein RAJ] Department of Radiology and Nuclear Medicine, University Medical Center Utrecht/Wilhelmina Children’s Hospital, Utrecht University, Utrecht, The Netherlands. Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands. [Watson TA] Department of Paediatric Radiology, Great Ormond Street Hospital NHS Foundation Trust, London, UK. [Brisse HJ] Imaging Department, Institut Curie, Paris, France. [Morosi C] Department of Radiology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy. [Lederman HM] Department of Diagnostic Imaging, Escola Paulista de Medicina, UNIFESP, São Paulo, Brazil. [Coma A] Servei de Radiologia Pediàtrica, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid34363274
dc.identifier.wos000682359900001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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