Clinical trial · Interventional
Etoposide in Treating Young Patients With Relapsed Ependymoma
Phase II Study of Intravenous Etoposide in Patients With Relapsed Ependymoma
NCT00278252CI-TRIAL-00011629unknownPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Drugs used in chemotherapy, such as etoposide, 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 etoposide works in treating young patients with ependymoma.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Brain and Central Nervous System Tumors | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| conventional surgery | Procedure | — | UNRESOLVED |
| etoposide | Drug | Etoposide | ALIAS |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Response rate by MRI after course 3
Secondary outcomes (1)
- measure
- Second surgery or additional radiotherapy in responding patients as assessed by MRI scan after course 3 or 6
Eligibility
Eligibility (as posted)
- Sex
- All
- Maximum age
- 21 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Histologically confirmed intracranial ependymoma at first, second, or third relapse * Anaplastic (malignant) or low-grade ependymoma (cellular, papillary, clear cell, or mixed variants) * Unequivocal evidence of tumor recurrence or progression by MRI scan after failing conventional treatment (e.g., primary surgery and adjuvant radiotherapy) for initial or recurrent disease * Unresectable disease OR not amenable to complete surgical resection * Measurable enhancing or non-enhancing disease on baseline scan performed within the past 2 weeks * Patients who have undergone prior surgery must have residual measurable disease PATIENT CHARACTERISTICS: * Lansky performance status 30-100% * Life expectancy ≥ 8 weeks * Absolute neutrophil count \> 1,000/mm\^3 * Platelet count \> 100,000/mm\^3 * Serum total bilirubin normal * AST \< 2 times upper limit of normal * No unrelated medical condition (e.g., renal or liver impairment) that would preclude chemotherapy treatment * No active infection * No known HIV positivity PRIOR CONCURRENT THERAPY: * See Disease Characteristics * No radiotherapy within the past 6 weeks * No chemotherapy within the past 4 weeks * Prior IV etoposide allowed
References
Publications (1)
- DERIVEDApps JR, Maycock S, Ellison DW, Jaspan T, Ritzmann TA, Macarthur D, Mallucci C, Wheatley K, Veal GJ, Grundy RG, Picton S. Phase II study of intravenous etoposide in patients with relapsed ependymoma (CNS 2001 04). Neurooncol Adv. 2022 Apr 13;4(1):vdac053. doi: 10.1093/noajnl/vdac053. eCollection 2022 Jan-Dec. PMID 35591977