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High-Dose Methotrexate in Treating Young Patients With Residual Ependymoma

Phase II Study of High-Dose Methotrexate in Children With Residual Ependymoma

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00287924
Enrollment
29
Registered
2006-02-07
Start date
2005-03-31
Completion date
Unknown
Last updated
2013-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain and Central Nervous System Tumors

Keywords

childhood infratentorial ependymoma, childhood supratentorial ependymoma, newly diagnosed childhood ependymoma

Brief summary

RATIONALE: Drugs used in chemotherapy, such as methotrexate, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. PURPOSE: This phase II trial is studying how well high-dose methotrexate works in treating young patients with residual ependymoma.

Detailed description

OBJECTIVES: Primary * Determine the activity of high-dose methotrexate as upfront-window therapy in young patients with residual ependymoma. Secondary * Assess the reasons why primary surgery was complete/incomplete in these patients. * Assess the feasibility and toxicity of second-look surgery after 3 courses of high-dose methotrexate in cases where initial surgery was incomplete. OUTLINE: This is a multicenter, open-label study. Patients receive high-dose methotrexate IV continuously over 24 hours on days 0, 14, and 28 in the absence of disease progression or unacceptable toxicity. Patients then proceed to further chemotherapy on protocol UKCCSG-CNS-9204. After completion of study treatment, patients are followed periodically for 9 years. PROJECTED ACCRUAL: A total of 29 patients will be accrued for this study.

Interventions

DRUGmethotrexate
PROCEDUREadjuvant therapy

Sponsors

Children's Cancer and Leukaemia Group
Lead SponsorOTHER

Study design

Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 2 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Histologically confirmed ependymoma, including the following histologic variants: * Cellular * Papillary * Clear-cell * Tanycytic * Anaplastic (malignant) ependymoma * The following diagnoses are excluded: * Myxopapillary ependymoma * Subependymomas * Ependymoblastomas * Primitive neuroectodermal tumors (PNETs) * Other neuroepithelial tumors * Choroid plexus tumors * Germ cell tumors * Residual measurable ependymoma after maximal surgical resection, including second-look surgery, if deemed necessary * Has undergone surgical resection within the past 3 weeks PATIENT CHARACTERISTICS: * At least 3 months to under 3 years of age * Neutrophil count \> 1,000/mm\^3 * Platelet count \> 100,000/mm\^3 * Able to tolerate chemotherapy * No co-existent unrelated disease (i.e., renal or hematological) that would preclude chemotherapy treatment PRIOR CONCURRENT THERAPY: * See Disease Characteristics * Recovered from prior surgery * No previous chemotherapy * Previous steroids allowed * No previous radiotherapy

Design outcomes

Primary

MeasureTime frame
Activity of high-dose methotrexate at 6 weeks

Secondary

MeasureTime frame
Assess reasons why primary surgery is complete or incomplete at diagnosis
Feasibility and toxicity of second look surgery after course 3 at 2 months
Compare functional imaging studies of ependymomas with biological characteristics of the tumors at diagnosis

Countries

Ireland, United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026