Radiation Therapy, Chemotherapy, and Peripheral Stem Cell Transplantation in Treating Patients With Primitive Neuroectodermal Tumors

Children's Oncology Group

Status and phase: Completed; Phase 2

Conditions: Neuroblastoma; Brain and Central Nervous System Tumors

Treatments: Drug: cyclophosphamide; Biological: filgrastim; Drug: thiotepa; Procedure: peripheral blood stem cell transplantation; Drug: vincristine sulfate; Radiation: radiation therapy; Drug: carboplatin; Procedure: bone marrow ablation with stem cell support

Study type: Interventional

Funder types: NETWORK; NIH

Identifiers

NCT00003846

99702

COG-99702 (Other Identifier)

CCG-99702 (Other Identifier)

CDR0000067006 (Other Identifier)

Details and patient eligibility

About

RATIONALE: Radiation therapy uses x-rays to damage tumor cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Peripheral stem cell transplantation may allow doctors to give higher doses of radiation therapy and chemotherapy and kill more tumor cells.

PURPOSE: Phase II trial to study the effectiveness of radiation therapy, chemotherapy and peripheral stem cell transplantation in treating patients with primitive neuroectodermal tumors.

Full description

OBJECTIVES:

• Determine the safety of postradiotherapy high-dose consolidation chemotherapy with peripheral blood stem cell (PBSC) support in patients with high-risk primitive neuroectodermal tumors.
• Determine the safety of delaying radiotherapy by approximately one month in these patients.
• Determine the maximum tolerated dose of thiotepa in these patients.
• Determine the toxic effects of intensive chemotherapy with PBSC support in these patients.
• Assess the time to hematopoietic recovery after PBSC infusion when intensive chemotherapy is used after craniospinal radiotherapy in these patients.
• Determine the overall and event-free survival of patients treated with this regimen.

OUTLINE: This is a dose-escalation study of thiotepa during consolidation therapy.

• Induction: Within 31 days of initial surgery, patients receive induction therapy comprising vincristine IV on day 0, cyclophosphamide IV over 2 hours on days 0 and 1, and filgrastim (G-CSF) subcutaneously (SC) beginning on day 2 and continuing for at least 7-10 days. Peripheral blood stem cells (PBSC) are then collected.
• Chemoradiotherapy: After blood cell counts recover, and within 28 days of starting induction, patients begin chemoradiotherapy. Patients receive vincristine IV once weekly for 8 doses. Radiotherapy is administered 5 days a week, for 6 weeks, beginning within the same week as the start of vincristine.
• Consolidation: Therapy begins 4-6 weeks after the last radiation treatment in the absence of disease progression. The first and third course are the same and comprise vincristine IV on day 0, carboplatin IV over 1 hour on days 0 and 1, thiotepa IV over 3 hours on days 2-4, and G-CSF SC daily beginning on day 7. PBSC are reinfused on day 7. The second course comprises vincristine IV on day 0, carboplatin IV over 1 hour on days 0 and 1, cyclophosphamide IV over 2 hours on days 2 and 3, and G-CSF SC daily beginning on day 5. PBSC are reinfused on day 5. Each course lasts 21 days.

For consolidation therapy, cohorts of 6-12 patients each receive escalating doses of thiotepa until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose at which no more than 2 of 12 patients experience dose-limiting toxicity.

Patients are followed every 3 months for 1 year, every 6 months for 2 years, and then annually thereafter.

PROJECTED ACCRUAL: A total of 24-56 patients will be accrued for this study.

Enrollment: 25 patients

Sex: All

Ages: 3 to 21 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Histologically proven primitive neuroectodermal tumor (PNET) of one of the following types:

  • Atypical teratoid/rhabdoid tumor
  • Medulloblastoma
  • Desmoplastic medulloblastoma
  • Ependymoblastoma
  • Medullomyoblastoma
  • Spongioblastoma
  • Spongioblastoma polare
  • Primitive polar spongioblastoma
  • Medulloepithelioma
  • Neuroblastoma
  • Pineoblastoma

• Posterior fossa PNET must be M1-3 or M0 with greater than 1.5 cm2 residual disease

• Non posterior fossa PNET and other types must be M0-3

  • If M3, must show clear evidence of tumor on MRI

• No marrow involvement or other extraneural metastases

• No M4 disease

• No cord compression requiring emergency radiotherapy

PATIENT CHARACTERISTICS:

Age:

• 3 to 21

Performance status:

• Not specified

Life expectancy:

• Not specified

Hematopoietic:

• Absolute neutrophil count at least 1,000/mm^3
• Platelet count at least 150,000/mm^3 (no platelet transfusions)
• Hemoglobin at least 10 g/dL (red blood cell transfusions allowed)

Hepatic:

• Bilirubin less than 1.5 times upper limit of normal (ULN)
• AST or ALT less than 2.5 times ULN

Renal:

• Creatinine clearance or glomerular filtration rate at least 70 mL/min

Cardiovascular:

• Shortening fraction greater than 27% by echocardiogram OR
• Ejection fraction greater than 47% by MUGA

Pulmonary:

• FEV_1/FVC greater than 60% except for children who:

  • Are uncooperative
  • Have no dyspnea at rest
  • Have no exercise intolerance
  • Have pulse oximetry greater than 94% on room air

Other:

• Not pregnant or nursing

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• Not specified

Chemotherapy:

• Not specified

Endocrine therapy:

• Steroids for increased intracranial pressure allowed

Radiotherapy:

• See Disease Characteristics
• No prior urgent radiotherapy

Surgery:

• Not specified

Other:

• No prior therapy for tumor

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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25 participants in 1 patient group

Treatment

Experimental group

Description:

See detailed description.

Treatment:

Radiation: radiation therapy

Procedure: bone marrow ablation with stem cell support

Procedure: peripheral blood stem cell transplantation

Drug: carboplatin

Drug: vincristine sulfate

Drug: thiotepa

Drug: cyclophosphamide

Biological: filgrastim