Trial | NCT00004224  Report issue

Title

Combination Chemotherapy Followed by Radiation Therapy in Treating Children With Localized Ependymoma
SIOP Study of Combined Modality Treatment in Childhood Ependymoma

  • Phase

    Phase 2

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    65
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining more than one drug and combining chemotherapy with radiation therapy may kill more tumor cells.

PURPOSE: This phase II trial is studying combination chemotherapy and radiation therapy to see how well they work in treating children with localized ependymoma.
OBJECTIVES:

Determine the event free and overall survival of children with incompletely resected localized ependymoma when treated with adjuvant cyclophosphamide, etoposide, and vincristine followed by radiotherapy.
Determine the response rate in these patients to this regimen.

OUTLINE: This is a multicenter study.

Patients undergo surgery to remove as much of tumor as possible. Patients with residual disease proceed to chemotherapy, while those with no residual disease proceed directly to radiotherapy.

Chemotherapy begins within 3 weeks of surgery and consists of vincristine IV on days 1, 8, and 15, cyclophosphamide IV over 3 hours on day 1, and etoposide IV over 4 hours on days 1-3. Treatment repeats every 4 weeks for up to 4 courses. Patients who progress after 2 courses proceed to radiotherapy. If residual disease is still present at completion of chemotherapy, second look surgery is recommended.

Patients undergo radiotherapy daily for 6 weeks beginning after complete resection within 4 weeks of surgery, within 3 weeks of completion of chemotherapy, or within 4 weeks of second look surgery.

Patients are followed at 6 weeks after radiotherapy, every 2 months for 1 year, every 4 months for 2 years, every 6 months for 2 years, and then annually for 5 years.

PROJECTED ACCRUAL: A total of 65 patients will be accrued for this study within 2-3 years.
Study Started
Jan 31
1999
Study Completion
Mar 31
2008
Last Update
Aug 26
2013
Estimate

Drug cyclophosphamide

Drug etoposide

Drug vincristine sulfate

Procedure adjuvant therapy

Procedure conventional surgery

Radiation radiation therapy

Criteria 

DISEASE CHARACTERISTICS:

Histologically proven nonmetastatic intracranial ependymoma

Cellular
Papillary
Clear cell
Mixed cell
Anaplastic
No myxopapillary ependymoma, subependymoma, or ependymoblastoma

PATIENT CHARACTERISTICS:

Age:

3 to 20

Performance status:

Not specified

Life expectancy:

Not specified

Hematopoietic:

No hematologic disease that would preclude study participation

Hepatic:

Not specified

Renal:

No renal disease that would preclude study participation

Other:

No concurrent unrelated disease that would preclude study participation

PRIOR CONCURRENT THERAPY:

Biologic therapy:

Not specified

Chemotherapy:

No prior chemotherapy

Endocrine therapy:

Prior steroids allowed

Radiotherapy:

No prior radiotherapy

Surgery:

Not specified
No Results Posted