Evidence map›Paper›PMID 41285272›Full record

Trial reportInternational journal of radiation oncology, biology, physics2026

Factors Associated With Primary Site Local Therapy in Patients With Nonmetastatic Ewing Sarcoma Treated With Interval-Compressed Chemotherapy: A Report From the Children's Oncology Group.

Safia K Ahmed, Odion Binitie, Mark Krailo, Daniel J Indelicato, Alexandra K Callan, Natalie DelRocco, Allen Buxton, Paul Chuba, Alexander Christ, Robert Lor Randall and 9 more

Abstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in International journal of radiation oncology, biology, physics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

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

19 authors.

Safia K AhmedDepartment of Radiation Oncology, Mayo Clinic, Phoenix, Arizona. Electronic address: ahmed.safia@mayo.edu.
Odion BinitieDepartment of Sarcoma, Moffitt Cancer Center, Tampa, Florida.
Mark KrailoDepartment of Population and Public Health Sciences, University of Southern California, Los Angeles, California.
Daniel J IndelicatoDepartment of Radiation Oncology, University of Florida, Jacksonville, Florida.
Alexandra K CallanDepartment of Orthopedic Surgery, UT Southwestern, Dallas, Texas.
Natalie DelRoccoDepartment of Population and Public Health Sciences, University of Southern California, Los Angeles, California.
Allen BuxtonChildren's Oncology Group, Operations Office, Monrovia, California.
Paul ChubaDepartment of Radiation Oncology, Ascension Health, Warren, Michigan.
Alexander ChristDepartment of Orthopedic Surgery, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.
Robert Lor RandallDepartment of Orthopedic Surgery, University of California, Davis, California.
Helen NadelDepartment of Radiology, Lucile Packard Children's Hospital Stanford University, Palo Alto, California.
Bruce PawelDepartment of Pathology, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.
Damon R ReedDivision of Pediatrics, Memorial Sloan Kettering Cancer Center, New York City, New York.
Richard G GorlickDivision of Pediatrics, University of Texas MD Anderson Cancer Center, Houston, Texas, United States.
Steven G DuBoisDepartment of Pediatrics, Dana-Farber/Boston Children's Cancer and Blood Disorders Center & Harvard Medical School, Boston, Massachusetts, United States.
Katherine A JanewayDepartment of Pediatrics, Dana-Farber/Boston Children's Cancer and Blood Disorders Center & Harvard Medical School, Boston, Massachusetts, United States.
Patrick J LeaveyDepartment of Pediatrics, UT Southwestern Medical Center Dallas and Children's Health, Children's Medical Center Dallas, Dallas, Texas.
Leo MascarenhasDepartment of Pediatrics, Guerin Children's and Cedars-Sinai Cancer, Cedars-Sinai Medical Center, Los Angeles, California.
Nadia N I LaackDepartment of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
NCI NIH HHS P30 CA008748NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

purposeLocal therapy (LT) is a critical component of curative treatment for Ewing sarcoma (ES). This analysis evaluated clinical and treatment variables associated with local failure (LF) risk for nonmetastatic patients with ES. METHODS AND MATERIALS: AEWS1031 was a phase 3 randomized trial comparing 2 interval-compressed chemotherapy regimens. Patients who completed induction chemotherapy and started LT of the primary tumor site were analyzed. LT was surgery alone (S), definitive radiation therapy (RT), or surgery and RT (S+RT), and was determined by the treating investigator. The primary endpoint was the cumulative incidence of LF estimated from the time LT was started. Elastic net penalization was used to identify predictors associated with the cause-specific hazard rates of LF.

resultsFive hundred eighty-eight patients started LT. Tumor sites were extremity (40%), axial (27%), pelvis (18%), and extraosseous (15%). LT was S (54%), RT (27%), and S+RT (18%). With a median follow-up of 67.6 months, the 5-year cumulative incidence of LF for all patients was 6%. LF incidence was 5% for S, 8.4% for RT, and 5.6% for S+RT (P = .47). LF incidence was 3.5% for extremity, 8.7% for pelvis, 7.7% for axial, and 6.3% for extraosseous (P = .09). LF incidence was higher for tumors ≥200 mL (11.3%) compared with tumors <200 mL (3.9%; P < .01). On multivariable modeling, increasing age at enrollment (cause-specific relative hazard ratio [csRHR] 1.04/y) and increasing maximum tumor dimension (csRHR 1.08/cm) were suggestive of a higher incidence of LF. By tumor subsite, axial tumors were associated with the highest risk of LF (csRHR 1.17) and extremity tumors with the lowest risk (csRHR 0.50).

conclusionsWe report the lowest LF incidence to date for prospective ES trials. Large tumors, older age, and axial tumor subsite were associated with higher LF incidence, indicating further efforts are needed to identify the highest-risk subset most likely to benefit from improved LT strategies.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBone NeoplasmsSarcoma, EwingAdolescentAdultAge FactorsChildChild, PreschoolFemaleHumansInduction ChemotherapyMaleTreatment FailureYoung Adult

Identifiers

PMID41285272
PMCPMC13052378

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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.