Clinical trial · Interventional
Salvage Therapy With Idarubicin in Relapsing CNS Lymphoma
Salvage Therapy With Idarubicin in Immunocompetent Patients With Relapsed or Refractory Primary Central Nervous System Lymphomas
NCT00210366CI-TRIAL-00003731terminatedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): due to slow accrual
Summary
Brief summary (as posted)
The main objective of the trial is to assess the therapeutic activity of idarubicin as salvage treatment in patients with recurrent or progressive lymphoma in the central nervous system.
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 |
|---|---|---|---|
| Lymphoma, B-Cell | B-Cell Malignant Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Idarubicin | Drug | Idarubicin | ALIAS |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- objective response to treatment
Secondary outcomes (3)
- measure
- duration of response
- measure
- overall survival
- measure
- acute side effects of idarubicin
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * Histological or cytological diagnosis of non-Hodgkin's lymphoma * Disease exclusively localised into the CNS at first diagnosis and failure * Progressive or recurrent disease * Previous treatment with HDMTX containing CHT and/or RT * Presence of at least one target lesion, bidimensionally measurable * Age 18 - 75 years * ECOG performance status \< 3 (Appendix 1). * No known HIV disease or immunodeficiency * HBsAg-negative and Ab anti-HCV-negative patients. * Adequate bone marrow function (plt \> 100000 mm3, Hb \> 9 g/dl, ANC \> 2.000 mm3) * Adequate renal function (serum creatinine \< 2 times UNL) * Adequate hepatic function (SGOT/SGPT \< 3 times UNL, bilirubin and alkaline phosphatase \< 2 times UNL) * Adequate cardiac function (VEF ≥ 50%) * Absence of any psycological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule * Non-pregnant and non-lactating status for female patients. Adequate contraceptive measures during study participation for sexually active patients of childbearing potential. * No previous or concurrent malignancies at other sites with the exception of surgically cured carcinoma in-site of the cervix and basal or squamous cell carcinoma of the skin and of other neoplasms without evidence of disease since at least 5 years. * No concurrent treatment with other experimental drugs. * Informed consent signed by the patient before registration
References
Publications (0)
Data not yet available
No reference posted for this study.