Evidence map›Paper›PMID 39080350›Full record

Trial reportBritish journal of cancer2024

Characteristics and outcome of synchronous bilateral Wilms tumour in the SIOP WT 2001 Study: Report from the SIOP Renal Tumour Study Group (SIOP-RTSG).

Hélène Sudour-Bonnange, Harm van Tinteren, Gema L Ramírez-Villar, Jan Godzinski, Sabine Irtan, Manfred Gessler, Tanzina Chowdhury, Georges Audry, Joerg Fuchs, Mark Powis and 14 more

Registry-linked trialAbstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in British journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00047138 (Nephroblastoma), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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.

NCT00047138 phase3unknown statusnot on this map

Nephroblastoma (Wilms Tumour) Clinical Trial And Study

TypeinterventionalSponsorUniversity of LeicesterRan2001Enrolled350ConditionsKidney CancerArmsdactinomycin, carboplatin, cyclophosphamide, doxorubicin hydrochloride, etoposide
3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Wilms tumor characteristics in children with heterozygous germline DIS3L2 variants.Genetics in medicine : official journal of the American College of Medical Genetics · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
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.

Hélène Sudour-BonnangeDepartment of Children and AYA Oncology, Centre Oscar Lambret, Lille, France. h-sudour@o-lambret.fr.ORCID http://orcid.org/0000-0002-1991-3585
Harm van TinterenPrincess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Gema L Ramírez-VillarDepartment of Pediatric Oncology, Hospital Universitario Virgen Del Rocio, Sevilla, Spain.
Jan GodzinskiDepartment of Pediatric Surgery, Marciniak Hospital, Fieldorfa 2 and Department of Pediatric Traumatology and Emergency Medicine, Wroclaw Medical university, Wrocław, Poland.
Sabine IrtanDepartment of Pediatric Surgery, Hospital Trousseau, Paris, France.
Manfred GesslerTheosor-Boveri Institute/Biocenter and Comprehensive Cancer Center Mainfranken, University of Wuerzburg, Würzburg, Germany.ORCID http://orcid.org/0000-0002-7915-6045
Tanzina ChowdhuryGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Georges AudryDepartment of Pediatric Surgery, Hospital Trousseau, Paris, France.
Joerg FuchsDepartment of Pediatric Surgery and Urology, University Hospital Tübingen, 72076, Tuebingen, Germany.
Mark PowisDepartment of Pediatric Surgery, Leeds Teaching Hospital NHS Trust, Leeds, UK.
Cornelis P van de VenPrincess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Bruce OkoyeDepartment of Paediatric Surgery, St George's University Hospital, London, UK.
Naima SmeuldersGreat Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
Gordan M VujanicDepartment of Pathology, Sidra Medicine and weill Cornell Medicine- Qatar, Doha, Qatar.ORCID http://orcid.org/0000-0003-0726-6939
Arnaud VerschuurDepartment of Pediatric Hemato-Oncology, Hospital La Timone, Marseille, France.
Aurore L'Herminé-CoulombDepartment of Pathology; Hospital Trousseau, Paris, France.
Beatriz de CamargoPediatric Hematology and Oncology program, research Center, Instituto National de Cancer, Rio de Janeiro, Brazil.
Joaquim Caetano de Aguirre NetoDepartment of Pediatric Hematology and Oncology, Hospital Santa Casa Belo-Horizonte, Belo Horizonte, Brazil.
Jens Peter SchenkSektion Pädiatrische Radiologie, Klinik für Diagnostische und Interventionelle Radiologie, Universitätsklinikum Heidelberg, Heidelberg, Deutschland.
Mary M van den Heuvel-EibrinkPrincess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-7760-879X
Katy Pritchard-JonesDevelopmental Biology and Cancer Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, University College London, London, UK.ORCID http://orcid.org/0000-0002-2384-9475
Norbert GrafSaarland University, Homburg, Germany.ORCID http://orcid.org/0000-0002-2248-323X
Christophe BergeronDepartment of Pediatric Oncology and Hematology, Centre Léon Berard, Lyon, France.
Rhoikos FurtwänglerSaarland University, Homburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmong patients with nephroblastoma, those with bilateral disease are a unique population where maximising tumour control must be balanced with preserving renal parenchyma.

methodsThe SIOP 2001 protocol recommended surgery after neoadjuvant cycle(s) of Dactinomycin and Vincristine (AV) with response-adapted intensification, if needed. Adjuvant treatment was given based on the lesion with the worst histology.

resultsThree hundred and twenty seven patients with stage V disease were evaluable: 174 had bilateral Wilms tumour (BWT), 101 unilateral WT and contralateral nephroblastomatosis (NB) and 52 bilateral nephroblastomatosis. In these three groups, the estimated 5y-EFS was 76.1%, 84.6%, and 74.9%, respectively. AV chemotherapy alone was the successful chemotherapy for 58.7% of all the patients and 65.6% of the non-metastatic patients. Among the 174 patients with BWT, 149 (88.2%) had at least one nephron-sparing surgery. Twenty of 61 bilateral stage I patients were treated with four-week AV postoperatively achieving 94.4% 5y-EFS. At last follow-up, 87% of patients had normal renal function.

conclusionsThis study demonstrates that AV without anthracyclines is sufficient to achieve NSS and good survival in the majority of patients. For patients with bilateral stage I WT and intermediate risk histology, only four weeks adjuvant AV seems to be sufficient. CLINICAL

trial registrationNCT00047138.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsDactinomycinKidney NeoplasmsVincristineWilms TumorChemotherapy, AdjuvantChildChild, PreschoolFemaleHumansInfantMaleNeoadjuvant TherapyNeoplasms, Multiple PrimaryNephrectomyTreatment OutcomeDactinomycinVincristine

Identifiers

PMID39080350
PMCPMC11405756

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Registered trials

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