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Feasibility of Using Concurrent Carboplatin and Reduced Dose Craniospinal Radiation (24Gy) for Metastatic Medulloblastoma, High-Risk Supratentorial PNET and Metastatic PNET


Phase 2
3 Years
25 Years
Open (Enrolling)
Both
Metastatic Medulloblastoma, High Risk Supratentorial PNET, Metastatic PNET

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Trial Information

Feasibility of Using Concurrent Carboplatin and Reduced Dose Craniospinal Radiation (24Gy) for Metastatic Medulloblastoma, High-Risk Supratentorial PNET and Metastatic PNET


Inclusion Criteria:



- Age greater than 3 years and less than 25 years

- Patients with classic histology or desmoplastic histology metastatic medulloblastoma
by histological diagnosis and by head and spine MRI.

- Patients with anaplastic histology will be excluded.

- Patients with high-risk supratentorial, non-metastatic, PNET

- Patients with metastatic PNET

- Newly diagnosed patients who have not received prior therapy, with the exception of
one short course of emergent chemotherapy in newly presenting patients with
neurological compromise per provider decision

- Only patients who are expected to survive at least 6 weeks will be eligible for this
study.

Exclusion Criteria:

- Patients who are pregnant may not be treated on this study

Type of Study:

Interventional

Study Design:

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Event-free Survival

Outcome Description:

MRIs of the head and spine

Outcome Time Frame:

up to 5 years

Safety Issue:

Yes

Authority:

United States: Institutional Review Board

Study ID:

06-1151

NCT ID:

NCT01542736

Start Date:

May 2007

Completion Date:

Related Keywords:

  • Metastatic Medulloblastoma
  • High Risk Supratentorial PNET
  • Metastatic PNET
  • Medulloblastoma
  • Neuroectodermal Tumors
  • Neuroectodermal Tumors, Primitive
  • Neuroectodermal Tumors, Primitive, Peripheral

Name

Location

Children's Hospital Colorado Aurora, Colorado  80045