RecruitingPhase 2NCT01356290

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

A Phase II Study of Metronomic and Targeted Anti-angiogenesis Therapy for Children With Recurrent/Progressive Medulloblastoma, Ependymoma, ATRT and Rare CNS Tumors


Sponsor

Medical University of Vienna

Enrollment

232 participants

Start Date

Apr 1, 2014

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Max Age: 19 Years

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGBevacizumab

10mg/kg, intravenous (iv), biweekly, 1 year

DRUGThalidomide

3mg/kg, oral, daily, 1 year

DRUGCelecoxib

50-400mg, oral bid, daily, 1 year

DRUGFenofibric acid

90mg/m2, oral, daily, 1 year

DRUGEtoposide

35-50 mg/m2, oral, alternating 21-day cycles of daily oral etoposide and cyclophosphamide, 1 year

DRUGCyclophosphamide

2.5mg/kg, oral, alternating 21-day cycles of daily oral etoposide and cyclophosphamide, 1 year

DRUGEtoposide phosphate

0.5mg, intrathecal, day 1-5, every four weeks, alternating with intrathecal liposomal cytarabine, 1 year

DRUGCytarabine

16-30mg, intrathecal, twice weekly for two weeks out of every four weeks, alternating with intrathecal etoposide phosphate, 1 year

DRUGTemozolomide (TMZ)

Stratum IV; 150mg/m2, day 1-5 every four weeks

DRUGIrinotecan

Stratum IV; 50mg/m2, day 1-5 every four weeks


Locations(22)

Ann & Robert H. Lurie Children's Hospital of Chicago

Chicago, Illinois, United States

Dana-Farber Cancer Institute and Boston Children's Hospital

Boston, Massachusetts, United States

Helen DeVos Children's Hospital

Grand Rapids, Michigan, United States

Dell Children's Medical Group SFC-HEM/ONC

Austin, Texas, United States

Medical University of Graz

Graz, Austria

Medical University of Innsbruck

Innsbruck, Austria

Kepler Universitätsklinikum Med Campus IV

Linz, Austria

Salzburger Universitätsklinikum

Salzburg, Austria

Medical University of Vienna

Vienna, Austria

University Hospital Brno

Brno, Czechia

Motol University Hospital Prague

Prague, Czechia

University hospital Rigshospitalet

Copenhagen, Denmark

Centre Oscar Lambret

Lille, France

Centre Léon Bérard

Lyon, France

Onkologisk-hematologisk seksjon Barneklinikken Haukeland universitetssjukehus

Bergen, Norway

Hospital Infantil Universitario Nino Jesus

Madrid, Spain

Sahlgrenska Universitetssjukhuset

Gothenburg, Sweden

Universitetssjukhuset Linköping

Linköping, Sweden

Skånes universitetssjukhus

Lund, Sweden

Karolinska University Hospital

Stockholm, Sweden

Norrlands Universitetssjukhus

Umeå, Sweden

Akademiska sjukhuset

Uppsala, Sweden

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT01356290


Related Trials