drugset / Trial / NCT00987636

Study in Localized and Disseminated Ewing Sarcoma

NCT00987636

Phase 3 Completed 907 enrolled University Hospital Muenster
RandomizedParallel-groupOpen-labelTreatment

Summary

Ewing Sarcoma Primary objectives: Standard Risk R1: in a randomised trial, to examine whether add-on treatment with zoledronic acid in addition to induction and maintenance chemotherapy improves event-free survival in patients with localised Ewing sarcoma and good histological response or with initial tumour volume \<200 mL compared to no add-on treatment. \*High Risk R2: in a randomised trial, to examine whether high-dose chemotherapy using busulfan-melphalan with autologous stem cell reinfusion, compared with standard chemotherapy, improves event-free survival in patients with localised Ewing sarcoma and poor histological response or tumour volume ≥200 mL (R2loc). In patients with pulmonary metastases high dose busulfan-melphalan chemotherapy with autologous stem cell reinfusion is randomised versus standard chemotherapy plus whole lung irradiation (R2pulm). Very High Risk R3: in a randomised trial, to examine whether the addition of high dose chemotherapy using treosulfan-melphalan followed by autologous stem cell reinfusion to eight cycles of standard adjuvant chemotherapy, compared to eight cycles of standard adjuvant chemotherapy alone, improves event-free survival in patients with primary disseminated disease. \*R2 accrual discontinued on December 1st 2015.

Timeline

Start
2009-10-01
Primary completion
2019-03-31
Completion
2019-03-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Busulfan Small molecule 0.8 mg/kg Intravenous
Subject Busulfan Small molecule 0.95 mg/kg Intravenous
Subject Busulfan Small molecule 1 mg/kg Intravenous
Subject Busulfan Small molecule 1.1 mg/kg Intravenous
Subject Busulfan Small molecule 1.2 mg/kg Intravenous
Subject Treosulfan Small molecule 12 g
Subject Zoledronic acid Other / unclassified 0.05 mg/kg Intravenous
Subject Zoledronic acid Other / unclassified 2 mg Intravenous
Subject Zoledronic acid Other / unclassified 4 mg Intravenous

Indications