Evidence map›Paper›PMID 39803937›Full record

ArticleCancer2025

Treatment of focal anaplastic Wilms tumor: A report from the Children's Oncology Group AREN0321 and AREN03B2 studies.

Amy E Armstrong, Najat C Daw, Lindsay A Renfro, James I Geller, John A Kalapurakal, Geetika Khanna, Arnold C Paulino, Elizabeth J Perlman, Peter F Ehrlich, Kenneth W Gow and 6 more

Abstract read
In one paragraph

Article in Cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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

16 authors.

Amy E ArmstrongDivision of Pediatric Hematology/Oncology, Washington University School of Medicine, St. Louis, Missouri, USA.ORCID https://orcid.org/0000-0002-7784-0476
Najat C DawDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Lindsay A RenfroDivision of Biostatistics, University of Southern California, Los Angeles, California, USA.
James I GellerDivision of Oncology, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA.ORCID https://orcid.org/0000-0001-5181-116X
John A KalapurakalDepartment of Radiation Oncology, Northwestern University, Chicago, Illinois, USA.
Geetika KhannaDepartment of Radiology and Imaging Sciences, Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
Arnold C PaulinoDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-0269-3045
Elizabeth J 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.ORCID https://orcid.org/0000-0001-6853-6221
Peter F EhrlichSection of Pediatric Surgery, University of Michigan, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0001-6161-1815
Kenneth W GowDivision of Pediatric Surgery, Stony Brook University, Stony Brook, New York, USA.
Anne B WarwickDepartment of Pediatrics, F. Edward Hébert School of Medicine, Uniformed Services University, Bethesda, Maryland, USA.
Paul E GrundyDivision of Immunology, Hematology, Oncology, Palliative Care, and Environmental Interactions, University of Alberta, Edmonton, Alberta, Canada.ORCID https://orcid.org/0000-0003-2645-8266
Conrad V FernandezDivision of Pediatric Hematology/Oncology, IWK Health Centre, Dalhousie University, Halifax, Nova Scotia, Canada.
Elizabeth A MullenDepartment of Pediatric Hematology/Oncology, Dana-Farber Cancer Institute and Boston Children's Hospital, Boston, Massachusetts, USA.
Jeffrey S DomeDivision of Oncology, Children's National Hospital and George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, USA.
Children's Oncology Group AREN0321 and AREN03B2 Study Committees

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
Children's Oncology Group Chair's Grant U10CA098543Children's Oncology Group NCTN Statistics & Data Center U10CA098413Children's Oncology Group NCTN Statistics & Data Center U10CA180899Human Specimen Banking in National Cancer Institute-Sponsored Clinical Trials 1U24-CA196173Human Specimen Banking in National Cancer Institute-Sponsored Clinical Trials U24CA114766National Cancer Institute Clinician Scientist Research Specialist Award R50CA275931National Cancer Institute's National Clinical Trial Network (NCTN) Operations Center U10CA180886NCI NIH HHS R50 CA275931NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS U24 CA114766NCI NIH HHS U24 CA196173St. Baldrick's Foundation
6 · The paper itself

Abstract

backgroundIn the fifth National Wilms Tumor Study, patients received vincristine and dactinomycin (VA) without radiation for stage I focal anaplastic Wilms tumor (FAWT) and VA plus doxorubicin (DD4A) and radiation for stage II-IV FAWT. Four-year event-free survival (EFS) and overall survival (OS) for stage I FAWT were 67.5% and 88.9% and for stage IV FAWT were 61.4% and 71.6%, respectively. Therapy intensification for stage I and IV FAWT was evaluated as secondary objectives in AREN0321.

methodsCentral review in the AREN03B2 Renal Tumors Classification, Biology, and Banking Study confirmed patient stage and tumor histology. Patients were then enrolled in AREN0321 and received DD4A with radiation for stage I-III FAWT and vincristine, doxorubicin, cyclophosphamide, carboplatin, and etoposide (UH-1/revised UH-1) with radiation for stage IV FAWT. Outcomes of patients with FAWT who were treated in AREN0321 (n = 25) and in AREN03B2 (n = 20) treated as per AREN0321 were analyzed.

resultsIn the pooled data analysis from AREN0321 and AREN03B2, 4-year EFS and OS were both 100% for stage I-II FAWT (n = 21), 82.4% (95% CI, 66.1%-100%) and 87.8% (95% CI, 73.4%-100%) for stage III FAWT (n = 17), respectively, and both 85.7% (95% CI, 63.3%-100%) for stage IV FAWT (n = 7). Four patients enrolled in AREN0321 had events: treatment failure occurred in three patients with stage III FAWT, and one treatment-related death was observed in a patient with stage IV FAWT following revised UH-1. No EFS or OS events occurred in patients with FAWT enrolled in AREN03B2 only.

conclusionsPatients with stage I and II FAWT have outstanding survival when treated with DD4A and radiation. Intensification of therapy may have improved survival for stage IV FAWT, albeit with an increased toxicity risk.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsKidney NeoplasmsWilms TumorCarboplatinChildChild, PreschoolCyclophosphamideDactinomycinDoxorubicinEtoposideFemaleHumansInfantMaleNeoplasm StagingVincristineCarboplatinCyclophosphamideDactinomycinDoxorubicinEtoposideVincristineanaplasiachemotherapyfocal anaplasiaradiation therapytreatmentWilms tumor

Identifiers

PMID39803937
PMCPMC12128929

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.