A Phase II Study of Metronomic and Targeted Anti-angiogenesis Therapy for Children with Recurrent/progressive Medulloblastoma, Ependymoma and ATRT

Who is this study for? Patients with Medulloblastoma
Status: Recruiting
Location: See all (22) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Patients with relapsed medulloblastoma, ependymoma and ATRT have a very poor prognosis whether treated with conventional chemotherapy, high-dose chemotherapy with stem cell rescue, irradiation or combinations of these modalities. Antiangiogenetic therapy has emerged as new treatment option in solid malignancies. The frequent, metronomic schedule targets both proliferating tumor cells and endothelial cells, and minimizes toxicity. In this study the investigators will evaluate the use of biweekly intravenous bevacizumab in combination with five oral drugs (thalidomide, celecoxib, fenofibrate, and alternating cycles of daily low-dose oral etoposide and cyclophosphamide), augmented with alternating courses of intrathecal etoposide and cytarabine. The aim of the study is to extend therapy options for children with recurrent or progressive medulloblastoma, ependymoma and ATRT, for whom no known curative therapy exists, by prolonging survival while maintaining good quality of life. The primary objective of the MEMMAT trial is to evaluate the activity of this multidrug antiangiogenic approach in these heavily pretreated children and young adults. Additionally, progression-free survival (PFS), overall survival (OS), as well as feasibility and toxicity will be examined.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 19
Healthy Volunteers: f
View:

• Relapsed or progressive medulloblastoma, ependymoma or ATRT (at least one site of untreated recurrent disease)

• Histological confirmation of medulloblastoma, ependymoma or ATRT at diagnosis or relapse

• Female or male, aged from 0 to \<20 years (at time of original diagnosis)

• Participants must have normal organ and bone marrow function (ALT \<5x institutional upper limit of normal, creatinine \<1.5x institutional upper limit of normal for age, WBC \>1000/mm3, platelets \> 20,000/mm3. Patients with values less than WBC 2000/mm3 or platelets 50,000/mm3 will require initiation of treatment with etoposide and cyclophosphamide at a lower starting dose as defined within the protocol.

• Karnofsky performance status ≥50. For infants and children less than 12 years of age, the Lansky play scale ≥50% will be used

• Written informed consent of patients and / or parents

Locations
United States
Illinois
Ann & Robert H. Lurie Children's Hospital of Chicago
TERMINATED
Chicago
Massachusetts
Dana-Farber Cancer Institute and Boston Children's Hospital
TERMINATED
Boston
Michigan
Helen DeVos Children's Hospital
RECRUITING
Grand Rapids
Texas
Dell Children's Medical Group SFC-HEM/ONC
RECRUITING
Austin
Other Locations
Austria
Medical University of Graz
RECRUITING
Graz
Medical University of Innsbruck
RECRUITING
Innsbruck
Kepler Universitätsklinikum Med Campus IV
RECRUITING
Linz
Salzburger Universitätsklinikum
RECRUITING
Salzburg
Medical University of Vienna
RECRUITING
Vienna
Czech Republic
University Hospital Brno
RECRUITING
Brno
Motol University Hospital Prague
RECRUITING
Prague
Denmark
University hospital Rigshospitalet
RECRUITING
Copenhagen
France
Centre Oscar Lambret
TERMINATED
Lille
Centre Léon Bérard
RECRUITING
Lyon
Norway
Onkologisk-hematologisk seksjon Barneklinikken Haukeland universitetssjukehus
RECRUITING
Bergen
Spain
Hospital Infantil Universitario Nino Jesus
RECRUITING
Madrid
Sweden
Sahlgrenska Universitetssjukhuset
RECRUITING
Göteborg
Universitetssjukhuset Linköping
RECRUITING
Linköping
Skånes universitetssjukhus
RECRUITING
Lund
Karolinska University Hospital
RECRUITING
Stockholm
Norrlands Universitetssjukhus
RECRUITING
Umeå
Akademiska sjukhuset
RECRUITING
Uppsala
Contact Information
Primary
Andreas Peyrl, MD
andreas.peyrl@meduniwien.ac.at
+43 1 40400
Backup
Irene Slavc, MD
irene.slavc@meduniwien.ac.at
+43 1 40400
Time Frame
Start Date: 2014-04
Estimated Completion Date: 2030-04
Participants
Target number of participants: 100
Sponsors
Leads: Medical University of Vienna

This content was sourced from clinicaltrials.gov

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