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Ewing sarcoma is described in the packet as a small round cell tumor that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. The packet states that it represents one of the two ends of the spectrum called Ewing sarcoma/peripheral neuroectodermal tumor, that it affects mostly males under age 20, and that it can occur in soft tissue or bone. The packet lists extraskeletal Ewing sarcoma and Ewing sarcoma of bone as subtypes. Prevalence is not certified in this packet.
The packet lists EWSR1 (chromosome 22) as an associated gene; no ClinGen validity classification is supplied for it, and the packet provides no molecular mechanism. The inheritance pattern listed in the packet is multifactorial. Further detail on causes is not certified in this packet.
The packet does not supply diagnostic criteria, testing methods, or newborn screening information for Ewing sarcoma. Diagnosis is therefore not certified in this packet.
The packet lists no FDA-approved treatments and no foundational therapies for Ewing sarcoma, so treatment coverage is not certified in this packet. The packet's orphan drug records include many entries with DESIGNATED status for treatment of Ewing sarcoma, including dinutuximab beta and padnarsertib, and WITHDRAWN entries including ganitumab and fenretinide; orphan designation is not approval.
100 trials found
The packet does not include natural history, survival, or outcome information for Ewing sarcoma. Prognosis is not certified in this packet.
The packet reports 94 active clinical trials for Ewing sarcoma on ClinicalTrials.gov, with intervention types including drug therapy, procedural interventions, biologic therapy, and other interventions, and the presence of gene therapy trials. Detailed records include NCT02306161, a Phase 3 study of combination chemotherapy with or without ganitumab in newly diagnosed metastatic Ewing sarcoma sponsored by the National Cancer Institute (active, not recruiting; 2014-12-12 to 2027-09-16); NCT05440786, a Phase 2 study of abemaciclib sponsored by Eli Lilly and Company (active, not recruiting); and NCT05968768, a Phase 2 study of naxitamab in refractory Ewing sarcoma (recruiting). Several listed records are Pediatric MATCH or pediatric solid tumor studies not specific to Ewing sarcoma. Titles alone do not establish the intervention studied. The packet's research landscape digest classifies 791 publications, with case reports and case series the dominant type.
Data assembled from 8 of 12 sources · Last updated Nov 3, 2026, 7:19 PM UTC
Patient Advocacy Groups (PAGs) provide support, resources, and community for patients and caregivers.
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center
AI-curated news mentioning Ewing sarcoma
Updated Oct 1, 2026
A recent study published in PubMed examines the long-term outcomes of Ewing sarcoma specifically in the foot and ankle. The findings contribute valuable insights into the prognosis and management of this rare bone cancer.
A case report highlights primary renal Ewing sarcoma with extensive metastatic disease at diagnosis, contributing to the understanding of this rare cancer. The literature review provides insights into treatment challenges and outcomes.
A case report highlights a rare instance of presumptive Ewing sarcoma of the jejunum with metastatic disease. This focused narrative review provides insights into the clinical presentation and management of this rare cancer type.