Evidence map›Paper›PMID 38973574›Full record

Trial reportInternational journal of cancer2024

Long-term outcomes and patterns of relapse in patients with bilateral Wilms tumor or bilaterally predisposed unilateral Wilms tumor, a report from the COG AREN0534 study.

Andrew J Murphy, Jack Brzezinski, Lindsay A Renfro, Brett Tornwall, Marcus M Malek, Daniel J Benedetti, Nicholas G Cost, Ethan A Smith, Jennifer Aldrink, Rodrigo L P Romao and 10 more

Abstract readMulticenter StudyClinical Trial, Phase III
In one paragraph

Trial report in International journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
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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

20 authors.

Andrew J MurphySt Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID 0000-0001-6747-0355
Jack BrzezinskiHospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Lindsay A RenfroDivision of Biostatistics, University of Southern California and Children's Oncology Group, Los Angeles, California, USA.
Brett TornwallDivision of Biostatistics, University of Southern California and Children's Oncology Group, Los Angeles, California, USA.
Marcus M MalekChildren's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Daniel J BenedettiMonroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Nicholas G CostThe Surgical Oncology Program at the Children's Hospital of Colorado, University of Colorado, Denver, Colorado, USA.
Ethan A SmithCincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Jennifer AldrinkDivision of Pediatric Surgery, Department of Surgery, Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, Ohio, USA.
Rodrigo L P RomaoHospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Jeffrey S DomeChildren National Hospital, George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Andrew M DavidoffSt Jude Children's Research Hospital, Memphis, Tennessee, USA.
Amy L TreeceAnn & Robert H. Lurie Children's Hospital, Chicago, Illinois, USA.
Lauren N ParsonsDepartment of Pathology, Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA.
Elizabeth A MullenBoston Children's Hospital and Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Robert C ShambergerBoston Children's Hospital and Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Arnold C PaulinoMD Anderson Cancer Center, Houston, Texas, USA.
Andrea C LoUniversity of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0002-3253-1071
James I GellerCincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Peter F EhrlichSection of Pediatric Surgery, CS Mott Children's Hospital, University of Michigan, Ann Arbor, Michigan, USA.

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Development, review, and conduct of Children's Oncology Group (COG) Clinical TrialsR50CA275931 · NCI · CHILDREN'S RESEARCH INSTITUTE · PI JEFFREY S DOME · 2023 to 2026
$569k
NCI NIH HHS R50 CA275931NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899St. Baldrick's FoundationUS National Institutes of Health/National Cancer Institute U10CA180886US National Institutes of Health/National Cancer Institute U10CA180899
6 · The paper itself

Abstract

The objective of this study is to report the long-term timing and patterns of relapse for children enrolled in Children's Oncology Group AREN0534, a multicenter phase III clinical trial conducted from 2009 to 2015. Participants included children with bilateral Wilms tumor (BWT) or unilateral WT with genetic predisposition to develop BWT followed for up to 10 years. Smoothed hazard (risk) functions for event-free survival (EFS) were plotted so that the timing of events could be visualized, both overall and within pre-specified groups. Two hundred and twenty-two children (190 BWT and 32 unilateral WT with BWT predisposition) were followed for a median of 8.6 years. Fifty events were reported, of which 48 were relapse/progression. The overall 8-year EFS was 75% (95% confidence interval: 69%-83%). The highest risk for an EFS event was immediately after diagnosis with a declining rate over 2 years. A second peak of events was observed around 4 years after diagnosis, and a small number of events were reported until the end of the follow-up period. In subset analyses, later increases in risk were more commonly observed in patients with female sex, anaplastic histology, negative lymph nodes or margins, and favorable histology Wilms tumor patients with post-chemotherapy intermediate risk. Among relapses that occurred after 2 years, most were to the kidney. These patterns suggest that late events may be second primary tumors occurring more commonly in females, although more investigation is required. Clinicians may consider observation of patients with BWT beyond 4 years from diagnosis.

Indexed as

Kidney NeoplasmsNeoplasm Recurrence, LocalWilms TumorChildChild, PreschoolFemaleFollow-Up StudiesGenetic Predisposition to DiseaseHumansInfantMalebilateral Wilms tumoreventslong‐term outcomespredispositionrelapse

Identifiers

PMID38973574
PMCPMC11570340

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Registered trials

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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.