Evidence map›Paper›PMID 41914453›Full record

ArticlePediatric blood & cancer2026

Intermediate Risk Rhabdomyosarcoma in Very Young Children (Less Than or Equal to 24 Months) Treated on the Prior Children's Oncology Group Protocol ARST1431.

Katrina Winsnes, Julie A Bradley, Zhengya Gao, Abha A Gupta, David H Rothstein, Archana Shenoy, Rajkumar Venkatramani, Wei Xue, Carola Arndt

Registry-linked trialAbstract read
In one paragraph

Article in Pediatric blood & cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02567435 (A Randomized Phase 3 Study of Vincristine, Dactinomycin, Cyclophosphamide), which is not on this map. Not yet cited in PubMed.

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

NCT02567435 phase3active not recruitingnot on this map

A Randomized Phase 3 Study of Vincristine, Dactinomycin, Cyclophosphamide (VAC) Alternating With Vincristine and Irinotecan (VI) Versus VAC/VI Plus Temsirolimus (TORI, Torisel, NSC# 683864) in Patients With Intermediate Risk (IR) Rhabdomyosarcoma (RMS)

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2016 to 2026Enrolled325ConditionsAlveolar Rhabdomyosarcoma, Botryoid-Type Embryonal Rhabdomyosarcoma, Embryonal Rhabdomyosarcoma, RhabdomyosarcomaArmsCyclophosphamide, Dactinomycin, Irinotecan Hydrochloride, Laboratory Biomarker Analysis, Questionnaire Administration
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Katrina WinsnesDepartment of Pediatrics, Oregon Health and Science University, Portland, Oregon, USA.ORCID https://orcid.org/0000-0002-9419-738X
Julie A BradleyDepartment of Radiation Oncology, University of Florida, Jacksonville, Florida, USA.
Zhengya GaoDepartment of Biostatistics, College of Public Health and Health Professions College of Medicine, University of Florida, Gainesville, Florida, USA.
Abha A GuptaDivision of Hematology/Oncology, Sickkids, University of Toronto, Ontario, Canada.
David H RothsteinDepartment of Pediatric General and Thoracic Surgery, Seattle Children's Hospital, Seattle, Washington, USA.
Archana ShenoyDivision of Pathology and Laboratory Medicine, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.
Rajkumar VenkatramaniDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Wei XueDepartment of Biostatistics, College of Public Health and Health Professions College of Medicine, University of Florida, Gainesville, Florida, USA.
Carola ArndtDivision of Pediatric Hematology/Oncology, Mayo Clinic, Rochester, Minnesota, 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
Friends of TJ FoundationMaddie's Promise FoundationNCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCTN Statistics & Data Center U10CA180899NIH HHS U10CA180886Sebastian Strong FoundationSt. Baldrick's FoundationSummer's Way Foundation
6 · The paper itself

Abstract

backgroundRhabdomyosarcoma is the most common soft tissue sarcoma in pediatrics and infants are reported to have inferior outcomes. ARST1431 recommended delayed primary excision (DPE) while discouraging radiation (RT) deviations. This analysis compared outcomes among very young and older patients in this study. PROCEDURES: Demographic and tumor characteristics were summarized using frequencies and percentages. Local failure (LF) frequency was summarized by age group, RT, and DPE status. Event-free survival (EFS) and overall survival (OS) were estimated using the Kaplan-Meier method and compared between age groups using the log-rank test.

resultsOf 296 patients, 48 (16.2%) were <24 months: 14 (4.7%) < 12 months, 34 (11.5%) 12-24 months-compared with 248 (83.8%) ≥24 months. DPE was performed in: 7 (50%), <12 months; 9 (26%), 12-24 months; 56 (22%), ≥24 months. RT was given to 9 (64%), 27 (79%), and 195 (79%) of <12, 12-24, and >24 months, respectively. LF in DPE+RT was 8.3% and 6.1%, < 24 months and ≥ 24 months, respectively, compared to 29.3% and 20.5% for RT without DPE. The 4-year EFS did not vary: 56% (95% CI = 26.5, 86.0), 68% (95% CI = 51.2, 84.1), and 61% (95% CI = 54.2, 68.3) <12, 12-24, and >24 months old, respectively.

conclusionsOutcomes in younger children are comparable to older children with local failure more common in those without DPE. Optimization of local control will be important for future studies. TRIAL REGISTRATION NUMBER: NCT02567435.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsRhabdomyosarcomaChild, PreschoolDisease-Free SurvivalFemaleFollow-Up StudiesHumansInfantMalePrognosisSurvival Rateinfantsrhabdomyosarcomayoung children

Identifiers

PMID41914453
PMCPMC13100859

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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.