Evidence map›Paper›PMID 42335412›Full record

ArticleJCO clinical cancer informatics2026

A Harmonized International Database of More Than 10,000 Pediatric Renal Tumor Patients From 30 Years of SIOP-RTSG Studies.

Prakriti Roy, Ingrid Schut, Norbert Graf, Arnauld Verschuur, Tanzina Chowdhury, Filippo Spreafico, Jesper Brok, Gema L Ramirez-Villar, Beatriz de Camargo, Jan Godzinski and 14 more

Abstract read
In one paragraph

Article in JCO clinical cancer informatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Prakriti RoyPrincess Maxima Center for Paediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0003-0086-6691
Ingrid SchutPrincess Maxima Center for Paediatric Oncology, Utrecht, the Netherlands.
Norbert GrafDepartment of Paediatric Oncology and Hematology, Saarland University, Homburg, Germany.ORCID 0000-0002-2248-323X
Arnauld VerschuurDepartment of Paediatric Oncology, Hôpital d'Enfants de la Timone, Marseille, France.ORCID 0000-0003-1070-4442
Tanzina ChowdhuryDepartment of Haematology and Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.ORCID 0000-0003-3891-5778
Filippo SpreaficoDepartment of Medical Oncology and Hematology, Paediatric Oncology Unit, Fondazione IRCCS Instituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-5587-3509
Jesper BrokDepartment of Paediatric Oncology and Hematology, Rigshospitalet, Copenhagen, Denmark.
Gema L Ramirez-VillarDepartment of Paediatric Oncology, Hospital Universitario Virgen del Rocío, Seville, Spain.ORCID 0000-0001-9986-5861
Beatriz de CamargoResearch Center, Instituto Nacional do Cancer, Rio de Janeiro, Brazil.ORCID 0000-0002-5794-1042
Jan GodzinskiDepartment of Paediatric Surgery, Marciniak Hospital, Wroclaw, Poland.ORCID 0000-0001-9687-7146
Gordan VujanicDepartment of Pathology, Sidra Medicine and Weill Cornell Medicine, Doha, Qatar.ORCID 0000-0003-0726-6939
Patrick MelchiorDepartment of Radiation Oncology, Saarland University Hospital, Homburg, Germany.
Ria KoolmaPrincess Maxima Center for Paediatric Oncology, Utrecht, the Netherlands.
Reem Al-SaadiDepartment of Haematology and Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.ORCID 0000-0002-0816-5649
Manfred GesslerTheodor-Boveri-Institute/Biocenter and Comprehensive Cancer Center Mainfranken, University of Würzburg, Würzburg, Germany.ORCID 0000-0002-7915-6045
Catriona DuncanDepartment of Haematology and Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.ORCID 0000-0002-9496-4745
Jens-Peter SchenkPaediatric Radiology Section, Department for Diagnostic and Interventional Radiology, University Hospital Heidelberg, Heidelberg, Germany.ORCID 0000-0002-0588-0225
Rhoikos FurtwänglerPaediatric Haematology and Oncology, Department of Paediatrics-Inselspital, University Bern, Bern, Switzerland.ORCID 0000-0002-1967-8343
Helene S BonnangeChildren and AYA Unit, Oscar Lambret Center, Lille, France.
Severine MetzgerDepartment of Clinical Research and Innovation, Centre Léon Bérard, Lyon, France.
Danny BaarsPrincess Maxima Center for Paediatric Oncology, Utrecht, the Netherlands.
Kathy Pritchard-JonesDevelopmental Biology and Cancer Research and Teaching Department, University College London Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0002-2384-9475
Marry M van den Heuvel-EibrinkPrincess Maxima Center for Paediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0002-7760-879X
Harm van TinterenPrincess Maxima Center for Paediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0002-4626-8702

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and scopeHistorical data sources for rare cancers are valuable for data-driven research. The International Society of Pediatric Oncology Renal Tumors Study Group (SIOP-RTSG) has been conducting clinical research on pediatric renal tumors for more than 50 years. Since 1993, data have been collected across multiple countries, using standardized paper-based case report forms that were digitally transcribed into electronic databases. Until 2019, prospectively collected data are present in nine different electronic sources from three consecutive clinical studies. More than 10,000 patient cases of kidney cancer in children are registered in totality. However, the necessary merging of numerous sources to answer a research question is repetitive, time consuming, and unsustainable in the long term. SOLUTION: By mapping and formatting the structure of these nine databases, a single database was created that was similar in design to the prospective study database. This allows the data from the past and current studies to be accessed and queried efficiently with standardized syntax and reports. EVALUATION: We validated this new database by reviewing whether uploads were complete and successful, mapped items were coded correctly, or discrepancy appeared in the export. Comparisons with retrospective reports were made to ensure the datasets were reproducible. RELEVANCE: Researchers have access to a large number of patients through this validated aggregated database. Data maintenance and extraction is efficient, and it offers the possibility to complete missing data directly into the central database. This ultimately ensures long-term availability in a secure, flexible, and responsible manner, in accordance with FAIR principles. HOW TO ACCESS/USE: Researchers can send questions to SIOP-RTSG and, if necessary, gain access to the database after short training. Access granted would depend on user's role.

Indexed as

Databases, FactualKidney NeoplasmsChildHumans

Identifiers

PMID42335412
PMCPMC13308643

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.