Evidence map›Paper›PMID 35129294›Full record

ReviewPediatric blood & cancer2022

An update on rhabdomyosarcoma risk stratification and the rationale for current and future Children's Oncology Group clinical trials.

Josephine H Haduong, Christine M Heske, Wendy Allen-Rhoades, Wei Xue, Lisa A Teot, David A Rodeberg, Sarah S Donaldson, Aaron Weiss, Douglas S Hawkins, Rajkumar Venkatramani

Open access · greenAbstract readReview
In one paragraph

Review in Pediatric blood & cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 1 pooled it
16.0field-weighted citation impact, top 1% 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.

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

76 citing papers in PubMed, 1 synthesis or guideline pooled it, 109 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Sarcomas in Adolescents and Young Adults.Current oncology reports · 2026
    Review
  14. Article
  15. Review
  16. Review
  17. CAR-T cell immunotherapy in rhabdomyosarcoma.Journal of translational medicine · 2026
    Review
  18. Article
  19. Predictors of survival in alveolar rhabdomyosarcoma in the US.Annals of medicine and surgery (2012) · 2026
    Article
  20. Article

16 more citing papers are in PubMed but not listed here.

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

10 authors at 10 institutions in 1 country.

Josephine H HaduongDivision of Oncology, Hyundai Cancer Institute, Children's Hospital Orange County, Orange, California, USA.ORCID 0000-0002-9135-7739
Christine M HeskePediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.
Wendy Allen-RhoadesDivision of Pediatric Oncology, Mayo Clinic, Rochester, Minnesota, USA.
Wei XueDepartment of Biostatistics, College of Public Health and Health Professions and College of Medicine, University of Florida, Gainesville, Florida, USA.
Lisa A TeotDepartment of Pathology, Boston Children's Hospital/Harvard Medical School, Boston, Massachusetts, USA.
David A RodebergDivision of Pediatric Surgery, East Carolina University, Greenville, North Carolina, USA.ORCID 0000-0003-3594-7547
Sarah S DonaldsonDepartment of Radiation Oncology, Stanford University, Stanford, California, USA.ORCID 0000-0001-7125-3118
Aaron WeissDivision of Pediatric Hematology-Oncology, Maine Medical Center, Portland, Maine, USA.
Douglas S HawkinsDivision of Hematology/Oncology, Seattle Children's Hospital, University of Washington, Seattle, Washington, USA.ORCID 0000-0003-3602-1375
Rajkumar VenkatramaniDepartment of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.
Baylor College of Medicine · USBoston Children's Hospital · USChildren's Hospital of Orange County · USEast Carolina University · USMaine Medical Center · USMayo Clinic · USNational Cancer Institute · USSeattle Children's Hospital · USStanford University · USUniversity of Florida · US

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
MaineHealth Cancer Care Network (MHCCN) and NCORP Activities across the LifespanUG1CA239771 · NCI · MAINEHEALTH · PI Leslie Bradford, Christine Lu-Emerson · 2019 to 2026
$7.9M
Development of biologic based therapies for rhabdomyosarcomaZIABC011745 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HESKE, CHRISTINE · 2017 to 2023
$1.1M
NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS UG1 CA239771
6 · The paper itself

Abstract

Children and adolescents with rhabdomyosarcoma (RMS) comprise a heterogeneous population with variable overall survival rates ranging between approximately 6% and 100% depending on defined risk factors. Although the risk stratification of patients has been refined across five decades of collaborative group studies, molecular prognostic biomarkers beyond FOXO1 fusion status have yet to be incorporated prospectively in upfront risk-based therapy assignments. This review describes the evolution of risk-based therapy and the current risk stratification, defines a new risk stratification incorporating novel biomarkers, and provides the rationale for the current and upcoming Children's Oncology Group RMS studies.

Indexed as

RhabdomyosarcomaRhabdomyosarcoma, EmbryonalAdolescentChildGene FusionHumansRisk AssessmentRisk FactorsMYOD1rhabdomyosarcomaTP53

Identifiers

PMID35129294
PMCPMC8976559
OpenAlexW4210837087

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.