Evidence map›Paper›PMID 40464368›Full record

ArticleCancer2025

Extremity rhabdomyosarcoma in children, adolescents and young adults: A report from Children's Oncology Group trials.

Sapna Oberoi, Wei Xue, Amira Qumseya, Thomas Scharschmidt, Odion Binitie, Joel I Sorger, Kiran A Kumar, Kenneth Wong, Sarah S Donaldson, Lisa Teot and 2 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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  5. 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

12 authors.

Sapna OberoiDepartment of Pediatrics and Child Health, University of Manitoba, Winnipeg, Manitoba, Canada.ORCID https://orcid.org/0000-0002-6071-0042
Wei XueDepartment of Biostatistics, College of Public Health and Health Professions College of Medicine, University of Florida, Gainesville, Florida, USA.
Amira QumseyaDepartment of Biostatistics, College of Public Health and Health Professions College of Medicine, University of Florida, Gainesville, Florida, USA.
Thomas ScharschmidtDepartment of Orthopedics, Division of Musculoskeletal Oncology, Nationwide Children's Hospital, Columbus, Ohio, USA.
Odion BinitieSarcoma Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Joel I SorgerDepartment of Pediatric Surgery, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
Kiran A KumarDepartment of Radiation Oncology, UT-Southwestern Medical Center, Dallas, Texas, USA.
Kenneth WongDepartment of Radiation Oncology, University of Southern California, Los Angeles, California, USA.
Sarah S DonaldsonDepartment of Radiation Oncology, Stanford University, Stanford, California, USA.
Lisa TeotDepartment of Pathology, Boston Children's Hospital/Harvard Medical School, Boston, Massachusetts, USA.
Erin R RudzinskiDepartment of Pathology and Laboratory Medicine, University of Indiana, Indianapolis, Indiana, USA.
Rajkumar VenkatramaniDivision of Hematology/Oncology, Department of Pediatrics, Texas Children's Cancer Center, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, 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
National Clinical Trials Network Operations CenterNational Clinical Trials Network Statistics & Data CenterNCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899St. Baldrick's Foundation
6 · The paper itself

Abstract

backgroundLong-term survival and prognostic factors for patients with extremity rhabdomyosarcoma (RMS) treated on contemporary Children's Oncology Group (COG) trials are unknown.

methodsData of extremity RMS patients enrolled on COG trials from 1998 to 2014 were analyzed to estimate event-free survival (EFS) and overall survival (OS), and factors associated with survival.

resultsThe authors identified 264 extremity RMS patients, 159 (60%) localized and 105 (40%) metastatic. The 5-year EFS and OS of patients with localized disease was 62.6% (54%, 71.2%), and 78.7% (71.4%, 85.9%) and of those with metastatic disease was 7.7% (2.2%, 13.2%) and 22.7% (13.9%, 31.4%). Age at diagnosis was associated with EFS, whereas both sex and age at diagnosis were associated with OS. In metastatic patients, a lower Oberlin score was associated with improved EFS and OS, and females had improved OS. The 5-year EFS of patients with localized disease treated on the D9803 trial was not statistically different from those treated on ARST0531, but 5-year OS was statistically superior (adjusted hazard ratio [adjHR] 0.43 [0.21, 0.86]) after adjusting for potential confounders. The 5-year EFS of group 3 patients undergoing delayed primary excision (DPE) with R0 margins was better than those with DPE with positive margins (adjHR 0.31 [0.11, 0.87]) and comparable to group 2 RMS patients.

conclusionsOutcomes for metastatic extremity RMS remain poor. Among patients with localized disease, younger age, female sex, and treatment on D9803 were associated with improved OS, whereas DPE with R0 margins led to better EFS compared to DPE with positive margins in group 3 patients.

Indexed as

ExtremitiesRhabdomyosarcomaAdolescentAdultChildChild, PreschoolFemaleHumansInfantMalePrognosisYoung Adultchemotherapychildrendelayed primary excisionlimbradiationrhabdomyosarcoma

Identifiers

PMID40464368
PMCPMC12135461

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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.