drugset / Trial / NCT01356290

Antiangiogenic Therapy for Children With Recurrent Medulloblastoma, Ependymoma, ATRT and Rare CNS Tumors

NCT01356290

Phase 2 Recruiting 232 enrolled Medical University of Vienna
RandomizedParallel-groupOpen-labelTreatment

Summary

Patients with with recurrent or progressive medulloblastoma, ependymoma, atypical teratoid rhabdoid tumor (ATRT), and CNS tumors of various histologies have a very poor prognosis whether treated with conventional chemotherapy, high-dose chemotherapy with stem cell rescue, irradiation or combinations of these modalities. Antiangiogenesis therapy has emerged as a new treatment option in solid malignancies. The frequent delivery of low doses of chemotherapy, referred to as metronomic or antiangiogenic chemotherapy, targets endothelial cells while reducing the toxicity associated with standard dose chemotherapy. The aim of the study is to extend therapy options for children with recurrent or progressive medulloblastoma, ependymoma, ATRT, and CNS tumors of various histologies, for whom no known curative therapy exists, by prolonging survival while maintaining good quality of life. The study will be conducted in independent strata. Stratum I (recurrent medulloblastoma): recently completed (Peyrl, 2023). Stratum II (recurrent ependymoma), III (recurrent ATRT) and V (recurrent CNS tumors of various histologies, patients with exclusion criteria and adult patients): The primary objective is to determine the response rate defined as the percentage of patients with complete response (CR), partial response (PR), stable disease (SD) or lack of recurrence at 6 months after start of antiangiogenic treatment. Stratum IV (recurrent medulloblastoma): To determine whether temozolomide, irinotecan, bevacizumab, thalidomide, celecoxib, fenofibrate, etoposide ivt, cytarabine ivt can increase the response rate after 6 months of treatment, compared with etoposid, cyclophosphamide, bevacizumab, thalidomide, celecoxib, fenofibrate, etoposide ivt, cytarabine ivt. Additionally, PFS, OS, toxicity, QoL, performance status, predictive and prognostic markers will be examined. In stratum II and III, the study will follow an open label, single arm phase 2 design, and an open label randomized two-arm phase 2 design in Stratum IV, and the exploratory Stratum V.

Timeline

Start
2014-04
Primary completion
2030-04
Completion
2030-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 10 mg/kg Intravenous
Subject Celecoxib Other / unclassified 50 mg Oral
Subject Celecoxib Other / unclassified 400 mg Oral
Subject Cyclophosphamide Other / unclassified 2.5 mg/kg Oral
Subject Cytarabine Small molecule 16 mg Intrathecal
Subject Cytarabine Small molecule 30 mg Intrathecal
Subject Etoposide Small molecule 0.5 mg Intrathecal
Subject Etoposide Small molecule 35 mg/m2 Oral
Subject Etoposide Small molecule 50 mg/m2 Oral
Subject Irinotecan Small molecule 50 mg/m2
Subject Temozolomide Small molecule 150 mg/m2
Subject Thalidomide Other / unclassified 3 mg/kg Oral
Subject fenofibric acid Small molecule 90 mg/m2 Oral