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Clinical Trials/NCT02025881
NCT02025881
Terminated
Phase 1

Phase I / II Study of Sequential High-dose Chemotherapy With Stem Cell Support in Children Younger Than 5 Years of Age With High-risk Medulloblastoma

Gustave Roussy, Cancer Campus, Grand Paris13 sites in 1 country29 target enrollmentSeptember 14, 2013

Overview

Phase
Phase 1
Intervention
Carboplatin + etoposide
Conditions
High-risk Medulloblastoma
Sponsor
Gustave Roussy, Cancer Campus, Grand Paris
Enrollment
29
Locations
13
Primary Endpoint
Phase I - Maximum Tolerated Dose
Status
Terminated
Last Updated
last year

Overview

Brief Summary

The trial includes i) the evaluation of the efficacy of a treatment strategy, designed as a phase II trial, and ii) a dose-finding part.

The Phase II trial is an open label, non-randomized, multicentre trial without control group. A Bayesian approach will be used to analyse the EFS, assuming a cure model. We will use three prior distributions of the EFS; (1) an enthusiastic prior distribution, (2) a pessimistic prior distribution, and (3) a non-informative prior distribution. As the patient outcomes in the trial will be recorded, the subsequent distribution of the outcome probability under experimental treatment will be computed by applying Bayes' theorem, which yields an estimated EFS probability with a 95% credibility interval (measure of Bayesian precision). Two interim analyses are planned to monitor the efficacy data (early stopping rules for futility or inefficacy).

The final analysis of efficacy will be made on an intention to treat basis, including all recruited patients, 3 years after recruitment of the last patient.

Due to the uncertainty on the dose of cyclophosphamide that can be given in combination with Busilvex for the last chemotherapy course in patients in complete response after intensification chemotherapy treatment, a dose-finding subtrial will be performed to address this issue (Phase I part). The dose escalation of cyclophosphamide will be performed using the Continual Reassessment Method in a Bayesian framework.

Registry
clinicaltrials.gov
Start Date
September 14, 2013
End Date
October 25, 2020
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Histological diagnosis of medulloblastoma with no INI-1 loss
  • High risk medulloblastoma defined by at least one of the following conditions:
  • Newly diagnosed classical metastatic medulloblastoma
  • Newly diagnosed anaplastic/large cell medulloblastoma or other unfavourable histology confirmed by review and coordinating investigator
  • Newly diagnosed medulloblastoma with amplification of c-myc or N-myc
  • Age at initial biopsy less or equal than 5 years
  • Weight compatible with leukapheresis
  • Ability to comply with requirements for submission of materials for central review
  • Nutritional and general status compatible with this therapy, Lansky play score \>/= 30%
  • Estimated life expectancy \>/=3 months

Exclusion Criteria

  • Desmoplastic medulloblastoma
  • Atypical Teratoid rhabdoid tumour
  • Uncontrolled active or symptomatic intracranial hypertension
  • Patient incapable of undergoing medical follow-up
  • Relapse of medulloblastoma

Arms & Interventions

Treatment

Carboplatin + etoposide then thiotepa then Cyclophosphamide + Busilvex. If insufficient response: TEMIRI + etoposide/radiotherapy + temozolomide

Intervention: Carboplatin + etoposide

Treatment

Carboplatin + etoposide then thiotepa then Cyclophosphamide + Busilvex. If insufficient response: TEMIRI + etoposide/radiotherapy + temozolomide

Intervention: Thiotepa

Treatment

Carboplatin + etoposide then thiotepa then Cyclophosphamide + Busilvex. If insufficient response: TEMIRI + etoposide/radiotherapy + temozolomide

Intervention: Cyclophosphamide + Busilvex

Treatment

Carboplatin + etoposide then thiotepa then Cyclophosphamide + Busilvex. If insufficient response: TEMIRI + etoposide/radiotherapy + temozolomide

Intervention: Temozolimide + Irinotecan

Treatment

Carboplatin + etoposide then thiotepa then Cyclophosphamide + Busilvex. If insufficient response: TEMIRI + etoposide/radiotherapy + temozolomide

Intervention: Etoposide + radiotherapy

Treatment

Carboplatin + etoposide then thiotepa then Cyclophosphamide + Busilvex. If insufficient response: TEMIRI + etoposide/radiotherapy + temozolomide

Intervention: Temozolomide

Outcomes

Primary Outcomes

Phase I - Maximum Tolerated Dose

Time Frame: From inclusion to the Dose Limiting Toxicity up to 12 months

To determine the Maximum Tolerated Dose (MTD) of cyclophosphamide in combination with a fixed dose of Busilvex in children with high-risk medulloblastoma who are in complete response after the intensification phase.

Phase II - Event Free Survival

Time Frame: From inclusion to Event up to 3 years

To assess the efficacy in terms of Event Free Survival (EFS) of the strategy intended to treat children younger than 5 years of age suffering from high-risk medulloblastoma with sequential high-dose chemotherapy without radiotherapy.

Secondary Outcomes

  • Radiotherapy-free survival without event(From inclusion up to 3 years)
  • Overall Survival(From inclusion up to 3 years)

Study Sites (13)

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