MRI Characteristics of Pediatric Renal Tumors: A SIOP-RTSG Radiology Panel Delphi Study.


Journal

Journal of magnetic resonance imaging : JMRI
ISSN: 1522-2586
Titre abrégé: J Magn Reson Imaging
Pays: United States
ID NLM: 9105850

Informations de publication

Date de publication:
02 2022
Historique:
revised: 28 07 2021
received: 17 06 2021
accepted: 28 07 2021
pubmed: 8 8 2021
medline: 1 2 2022
entrez: 7 8 2021
Statut: ppublish

Résumé

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. To identify MRI characteristics that may be used for discrimination of newly diagnosed pediatric renal tumors. Consensus process using a Delphi method. Not applicable. Abdominal MRI including T1- and T2-weighted imaging, contrast-enhanced MRI, and diffusion-weighted imaging at 1.5 or 3 T. 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. 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. 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. 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. 3 Technical Efficacy Stage: 3.

Sections du résumé

BACKGROUND
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.
LEVEL OF EVIDENCE
3 Technical Efficacy Stage: 3.

Identifiants

pubmed: 34363274
doi: 10.1002/jmri.27878
pmc: PMC9291546
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

543-552

Informations de copyright

© 2021 The Authors. Journal of Magnetic Resonance Imaging published by Wiley Periodicals LLC on behalf of International Society for Magnetic Resonance in Medicine.

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Auteurs

Justine N van der Beek (JN)

Department of Radiology and Nuclear Medicine, University Medical Center Utrecht/Wilhelmina Children's Hospital, Utrecht University, Utrecht, The Netherlands.
Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Tom A Watson (TA)

Department of Paediatric Radiology, Great Ormond Street Hospital NHS Foundation Trust, London, UK.

Rutger A J Nievelstein (RAJ)

Department of Radiology and Nuclear Medicine, University Medical Center Utrecht/Wilhelmina Children's Hospital, Utrecht University, Utrecht, The Netherlands.
Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Hervé J Brisse (HJ)

Imaging Department, Institut Curie, Paris, France.

Carlo Morosi (C)

Department of Radiology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Henrique M Lederman (HM)

Department of Diagnostic Imaging, Escola Paulista de Medicina, UNIFESP, São Paulo, Brazil.

Ana Coma (A)

Department of Pediatric Radiology, Hospital Vall d'Hebron, Barcelona, Spain.

Maria M Gavra (MM)

Department of Pediatric Radiology and Nuclear Medicine, 'Aghia Sophia' Children's Hospital, Athens, Greece.

Kristina Vult von Steyern (K)

Center for Medical Imaging and Physiology, Skåne University Hospital, Lund University, Lund, Sweden.

Karoly Lakatos (K)

Department of Radiology, St. Anna Children's Hospital, University Clinic of Pediatrics, Medical University of Vienna, Vienna, Austria.

Luc Breysem (L)

Department of Radiology, University Hospitals Leuven, Leuven, Belgium.

Edit Varga (E)

Department of Pediatrics, Semmelweis University, Budapest, Hungary.

Hubert Ducou Le Pointe (H)

Department of Pediatric Imaging, Hôpital d'Enfants Armand-Trousseau APHP, Paris, France.

Maarten H Lequin (MH)

Department of Radiology and Nuclear Medicine, University Medical Center Utrecht/Wilhelmina Children's Hospital, Utrecht University, Utrecht, The Netherlands.
Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Jürgen F Schäfer (JF)

Division of Pediatric Radiology, Department of Radiology, University Hospital Tübingen, Tübingen, Germany.

Hans-Joachim Mentzel (HJ)

Section of Pediatric Radiology, Institute of Diagnostic and Interventional Radiology, University Hospital Jena, Jena, Germany.

Andreas M Hötker (AM)

Institute of Diagnostic and Interventional Radiology, University Hospital Zurich, Zurich, Switzerland.

Giuseppina Calareso (G)

Radiology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Sophie Swinson (S)

Department of Paediatric Radiology, Leeds Teaching Hospitals, Leeds, UK.

Martin Kyncl (M)

Department of Radiology, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.

Claudio Granata (C)

Department of Paediatric Radiology, Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.

Michael Aertsen (M)

Department of Radiology, University Hospitals Leuven, Leuven, Belgium.

Pier Luigi Di Paolo (PL)

Department of Radiology, Bambino Gesù Children's Hospital, Rome, Italy.

Ronald R de Krijger (RR)

Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.

Norbert Graf (N)

Department of Pediatric Oncology & Hematology, Saarland University Medical Center and Saarland University Faculty of Medicine, Homburg, Germany.

Øystein E Olsen (ØE)

Department of Paediatric Radiology, Great Ormond Street Hospital NHS Foundation Trust, London, UK.

Jens-Peter Schenk (JP)

Clinic of Diagnostic and Interventional Radiology, Division of Pediatric Radiology, Heidelberg University Hospital, Heidelberg, Germany.

Marry M van den Heuvel-Eibrink (MM)

Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Annemieke S Littooij (AS)

Department of Radiology and Nuclear Medicine, University Medical Center Utrecht/Wilhelmina Children's Hospital, Utrecht University, Utrecht, The Netherlands.
Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

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