Evidence map›Paper›PMID 37933882›Full record

Trial reportCancer2024

Treatment of children with favorable histology Wilms tumor with extrapulmonary metastases: A report from the COG studies AREN0533 and AREN03B2 and NWTSG study NWTS-5.

Daniel J Benedetti, Carly R Varela, Lindsay A Renfro, Brett Tornwall, David B Dix, Peter F Ehrlich, Richard D Glick, John Kalapurakal, Elizabeth Perlman, Eric Gratias and 8 more

3 registry-linked trialsOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% of its field
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.

NCT00002611 phase3completednot on this map

National wilms tumor study-5 -- therapeutic trial and biology study

TypeinterventionalSponsorChildren's Oncology GroupRan1995 to 2003Enrolled3,031ConditionsKidney CancerArmsdactinomycin, filgrastim, cyclophosphamide, doxorubicin hydrochloride, etoposide
NCT00379340 phase3completednot on this map

Treatment of Newly Diagnosed Higher Risk Favorable Histology Wilms Tumors

TypeinterventionalSponsorChildren's Oncology GroupRan2007 to 2026Enrolled395ConditionsStage III Kidney Wilms Tumor, Stage IV Kidney Wilms TumorArms3-Dimensional Conformal Radiation Therapy, Conventional Surgery, Cyclophosphamide, Dactinomycin, Doxorubicin Hydrochloride
NCT00898365 completednot on this map

Renal Tumors Classification, Biology, and Banking Study

TypeobservationalSponsorChildren's Oncology GroupRan2006 to 2026Enrolled8,000ConditionsAdult Cystic Nephroma, Anaplastic Kidney Wilms Tumor, Angiolipoma, Cellular Congenital Mesoblastic NephromaArmsCytology Specimen Collection Procedure, Laboratory Biomarker Analysis
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. 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

18 authors at 16 institutions in 3 countries.

Daniel J BenedettiDivision of Hematology/Oncology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID 0000-0003-1524-3518
Carly R VarelaDivision of Hematology and Oncology, Pediatric Specialists of Virginia, Inova Fairfax Hospital, Fairfax, Virginia, USA.
Lindsay A RenfroDivision of Biostatistics, University of Southern California, Los Angeles, California, USA.
Brett TornwallGlaukos Corp., San Clemente, California, USA.
David B DixDivision of Oncology, British Columbia Children's Hospital, Vancouver, British Columbia, Canada.
Peter F EhrlichSection of Pediatric Surgery, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0001-6161-1815
Richard D GlickDivision of Pediatric Surgery, Zucker School of Medicine at Hofstra/Northwell, Cohen Children's Medical Center, New Hyde Park, New York, USA.
John KalapurakalDepartment of Radiation Oncology, Northwestern University, Chicago, Illinois, USA.
Elizabeth PerlmanDepartment of Pathology and Laboratory Medicine, Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Eric GratiaseviCore Healthcare, Bluffton, South Carolina, USA.
Nita L SeibelDivision of Cancer Treatment and Diagnosis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.ORCID 0000-0001-6259-7955
James I GellerDivision of Oncology, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA.ORCID 0000-0001-5181-116X
Geetika KhannaDepartment of Radiology & Imaging Sciences, Emory University, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
Marcio MalogolowkinDivision of Pediatric Hematology-Oncology, UC Davis Comprehensive Cancer Center, Sacramento, California, USA.
Paul GrundyDivision of Immunology, Hematology, Oncology, Palliative Care and Environmental Interactions, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0003-2645-8266
Conrad V FernandezDivision of Pediatric Hematology/Oncology, IWK Health Centre, Dalhousie University, Halifax, Nova Scotia, Canada.
Jeffrey S DomeDivision of Oncology, Children's National Hospital and the George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, USA.
Elizabeth A MullenDepartment of Pediatric Hematology/Oncology, Dana-Farber Cancer Institute/Boston Children's Hospital, Boston, Massachusetts, USA.
George Washington University Hospital · USNorthwestern University · USBC Children's Hospital · CABluffton University · USBoston Children's Hospital · USChildren's Oncology Group · CHCincinnati Children's Hospital Medical Center · USCohen Children's Medical Center · USDalhousie University · CAEmory University · USGlaukos (United States) · USNational Institutes of Health · USUniversity of Alberta · CAUniversity of California Davis Medical Center · USUniversity of Michigan · USVanderbilt University Medical Center · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ANDERSON, JAMES R · 2003 to 2013
$67.5M
COG U24 Funding 2026-2027U24CA196173 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI Mignon Lee-Cheun Loh, Nilsa Del Carmen Ramirez Milan · 2015 to 2026
$62.5M
Support for Human Specimen Banking in NCI-Supported Cancer Clinical TrialsU24CA114766 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI RAMIREZ MILAN, NILSA DEL CARMEN · 2005 to 2014
$14.5M
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 CA098413NCI NIH HHS U10CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10CA180886NCI NIH HHS U10 CA180899NCI NIH HHS U10CA180899NCI NIH HHS U10CA180899-06NCI NIH HHS U24 CA114766NCI NIH HHS U24CA114766NCI NIH HHS U24 CA196173NCI NIH HHS U24CA196173
6 · The paper itself

Abstract

backgroundPatients with stage IV favorable histology Wilms tumor (FHWT) with extrapulmonary metastases (EPM) constitute a small subset of patients with FHWT. Because of their rarity and heterogeneity, optimal FHWT treatment is not well understood. Children's Oncology Group protocol AREN0533 assigned patients with FHWT and EPM to intensified chemotherapy, regimen M, after initial DD-4A chemotherapy. To improve understanding of prognostic factors and best therapies, experiences of patients with EPM on AREN0533, as well as on protocols AREN03B2 and NWTS-5, were reviewed.

methodsCombined outcomes for patients with EPM from NWTS-5, AREN0533, and AREN03B2 were determined. Those treated on AREN0533 were compared with those treated on NWTS-5. Prognostic factors were explored in the pooled cohort.

resultsForty-seven patients with FHWT with EPM enrolled on AREN0533, 37 enrolled on NWTS-5, and 64 were followed only on AREN03B2. The pooled cohort of all 148 patients demonstrated a 4-year event-free survival (EFS) of 77.3% (95% CI, 70.8-84.4) and 4-year overall survival of 88.9% (95% CI, 83.9-94.2). Four-year EFS of patients with EPM treated on AREN0533 was 76.0% (95% CI, 64.6-89.4) vs 64.9% (95% CI, 51.7-82.2) on NWTS-5; hazard ratio, 0.64, p = .26; no difference in overall survival was observed. Increasing linear age and slow incomplete lung response were associated with worse EFS in a pooled cohort.

conclusionsOutcomes for patients with EPM are among the lowest for children with FHWT. Further trials with standardized surgical and radiation treatment to metastatic sites, and prospectively collected biologic and treatment details are needed. CLINICAL

trial registrationClinical Trials.gov identifiers: NCT00379340, NCT00898365, and NCT00002611.

Indexed as

Kidney NeoplasmsWilms TumorAntineoplastic Combined Chemotherapy ProtocolsChildHumansNeoplasm StagingProgression-Free SurvivalThoraxextrapulmonary metastasesmetastatic WilmsWilms tumor

Identifiers

PMID37933882
PMCPMC10922062
OpenAlexW4388454615

What OpenQuestion holds

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Registered trials

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.