Evidence map›Paper›PMID 41183255›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2025

Molecular Characterization Informs Prognosis in Patients With Localized Ewing Sarcoma: A Report From the Children's Oncology Group.

Riaz Gillani, David S Shulman, Natalie J DelRocco, Kelly Klega, Ruxu Han, Mark D Krailo, Jonathan C Slack, Mohammad Tanhaemami, Abigail Ward, Victoria Bainer and 11 more

Abstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Long-Term Analysis of Patients With Ewing Sarcoma Included in the Euro-EWING99 Study.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
  4. Article
  5. Article
  6. STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Riaz GillaniDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-8643-2725
David S ShulmanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.
Natalie J DelRoccoChildren's Oncology Group, Monrovia, CA.ORCID 0000-0002-8139-9839
Kelly KlegaDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-3424-2003
Ruxu HanChildren's Oncology Group, Monrovia, CA.
Mark D KrailoChildren's Oncology Group, Monrovia, CA.
Jonathan C SlackRobert J. Tomsich Institute of Pathology and Laboratory Medicine, Cleveland Clinic, Cleveland, OH.
Mohammad TanhaemamiDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-6498-1181
Abigail WardDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.
Victoria BainerDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.
Cora RickerDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0003-1202-5603
Josee SparksBiopathology Center, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH.
Kelly M BaileyUniversity of Pittsburgh School of Medicine, Pittsburgh, PA.ORCID 0000-0003-3925-3243
Damon R ReedDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-8238-2465
Steven G DuBoisDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0003-0882-738X
Patrick LeaveyDepartment of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0002-0541-2536
Leo MascarenhasCedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0001-7790-0777
Patrick J GroharDepartment of Pediatrics, Division of Pediatric Hematology Oncology, University of Michigan Medical School, CS Mott Children's Hospital, Ann Arbor, MI.ORCID 0000-0002-1071-4563
Alanna J ChurchHarvard Medical School, Boston, MA.ORCID 0000-0002-4835-5770
Brian D CromptonDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-9404-6621
Katherine A JanewayDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-6000-3594

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
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
Dissecting the role of DNA damage repair deficiency in Ewing sarcoma pathogenesis for improved risk stratification and treatmentK08CA276701 · NCI · DANA-FARBER CANCER INST · PI Riaz Gillani · 2023 to 2026
$788k
NCI NIH HHS K08 CA276701NCI NIH HHS P30 CA008748NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS U24 CA196173
6 · The paper itself

Abstract

purposeIdentifying discrete subgroups associated with treatment response and resistance in localized Ewing sarcoma (EWS) remains a challenge. The primary objective of the Children's Oncology Group (COG) biology study AEWS18B1-Q was to molecularly characterize patients with localized EWS on prospective modern-day trials. PATIENTS AND

methodsWe analyzed clinical and molecular features from patients with localized EWS enrolled on frontline COG trials. All patients had available formalin-fixed paraffin-embedded (FFPE) tissue, frozen tissue, or whole-genome-amplified material. Sequencing was performed for identification of canonical fusions, recurrent copy number alterations (CNAs), and alterations in

resultsThree hundred fifty-one patients had sufficient tissue, which in most cases was extracted from two FFPE slides. EWS canonical fusions were identified in 282 patients (80.3%). Pathogenic mutations in

conclusionThis is a prospective validation of the molecular prognostic features of patients with localized EWS receiving standard-of-care therapy on therapeutic clinical trials. Building on previous work, patients with

Indexed as

Biomarkers, TumorBone NeoplasmsSarcoma, EwingAdolescentAdultChildChild, PreschoolCohesinsDNA Copy Number VariationsFemaleHumansInfantMaleMutationPrognosisProspective StudiesBiomarkers, TumorCohesinsSTAG2 protein, humanTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID41183255
PMCPMC12614438

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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.