Skip to content

International Euro Ewing (iEuroEwing) trial for treatment optimisation in patients with Ewing sarcoma

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2022-501180-40-00
Acronym
iEuroEwing
Enrollment
856
Registered
2023-04-03
Start date
2022-06-17
Completion date
Unknown
Last updated
2025-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ewing Sarcoma

Brief summary

iEuroEwing-SR: Analysis of EFS, iEuroEwing-SR-RT: Analysis of the occurrence of acute skin toxicity CTCAE grade ≥3 during radiotherapy, iEuroEwing-HR: Analysis of EFS

Detailed description

iEuroEwing-SR part: Investigation if the maintenance therapy with VinoCyc in a randomised design compared to the standard VDC/IE treatment alone improves overall survival (OS) since randomisation 2, aiming at a 10% increase, and whether the 3-year OS improves compared to historical controls., iEuroEwing-SR-RT part: Investigation if a higher dose of radiation improves local control since randomisation 1 and if a higher dose of radiation improves EFS and OS since randomisation 1., iEuroEwing-HR part: Investigation if the maintenance therapy with VinoCyc in a randomised design compared to the standard VDC/IE treatment alone improves OS, aiming at a 15% increase, and whether the 3-year OS improves compared to historical controls., Toxicity / Safety, Survival outcome, Quality of life, Time to diagnosis, Cancer predisposition, Correlation of histopathological, Biology of Ewing sarcoma

Interventions

DRUGFILGRASTIM
DRUGMESNA
DRUGIFOSFAMIDE
DRUGCYCLOPHOSPHAMIDE
DRUGDOXORUBICIN
DRUGETOPOSIDE
DRUGVINORELBINE
DRUGVINCRISTINE SULFATE

Sponsors

GPOH gGmbH
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
0 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
iEuroEwing-SR: Analysis of EFS, iEuroEwing-SR-RT: Analysis of the occurrence of acute skin toxicity CTCAE grade ≥3 during radiotherapy, iEuroEwing-HR: Analysis of EFS

Secondary

MeasureTime frame
iEuroEwing-SR part: Investigation if the maintenance therapy with VinoCyc in a randomised design compared to the standard VDC/IE treatment alone improves overall survival (OS) since randomisation 2, aiming at a 10% increase, and whether the 3-year OS improves compared to historical controls., iEuroEwing-SR-RT part: Investigation if a higher dose of radiation improves local control since randomisation 1 and if a higher dose of radiation improves EFS and OS since randomisation 1., iEuroEwing-HR part: Investigation if the maintenance therapy with VinoCyc in a randomised design compared to the standard VDC/IE treatment alone improves OS, aiming at a 15% increase, and whether the 3-year OS improves compared to historical controls., Toxicity / Safety, Survival outcome, Quality of life, Time to diagnosis, Cancer predisposition, Correlation of histopathological, Biology of Ewing sarcoma

Countries

Austria, Belgium, Finland, Germany, Greece, Hungary, Poland, Sweden

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026