drugset / Trial / NCT02066220

International Society of Paediatric Oncology (SIOP) PNET 5 Medulloblastoma

NCT02066220

RandomizedParallel-groupOpen-labelTreatment

Summary

The study PNET 5 MB has been designed for children with medulloblastoma of standard risk (according to the risk-group definitions which have been used so far; e.g. in PNET 4). With the advent of biological parameters for stratification into clinical medulloblastoma trials, the ß-catenin status will be the only criterion according to which study patients will be assigned to either treatment arm PNET 5 MB - LR or to PNET 5 MB - SR, respectively. The initial diagnostic assessments (imaging, staging, histology, and tumor biology) required for study entry are the same for both treatment arms. With the amendment for version 12 of the protocol, patients who have a WNT-activated medulloblastoma with clinically high-risk features can be included in the PNET 5 MB WNT-HR study, and patients with a high-risk SHH medulloblastoma with TP53 mutation (both somatic or germline including mosaicism) can be included in the PNET5 MB SHH-TP53 study. Data on patients with pathogenic germline alteration or cancer predisposition syndrome, who cannot be included in any prospective trial due to unavailability or due to physician or family decision, can be documented within the observational PNET 5 MB registry.

Timeline

Start
2014-06
Primary completion
2026-12
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboplatin Small molecule 200 mg/m2 Other
Subject Cisplatin Other / unclassified 70 mg/m2
Subject Cyclophosphamide Other / unclassified 1000 mg/m2
Subject Doxorubicin Other / unclassified 37.5 mg/m2 Other
Subject Lomustine Small molecule 75 mg/m2
Subject MTX Unknown 2 mg Other
Subject MTX Unknown 5 g Other
Subject Vinblastin Unknown 5 mg/m2
Subject Vincristine Small molecule 1.5 mg/m2
Background Leucovorin Small molecule

Indications