Clinical trial · Interventional
Combination Chemotherapy Plus Rituximab in Treating Patients With Recurrent or Refractory Non-Hodgkin's Lymphoma
A Phase II Trial of Ifosfamide, Carboplatin, and Etoposide (ICE) Chemotherapy in Combination With Rituximab as Salvage Therapy
- 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 use different ways to stop cancer cells from dividing so they stop growing or die. Monoclonal antibodies such as rituximab can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy combined with rituximab in treating patients who have recurrent or refractory non-Hodgkin's lymphoma.
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 | Lymphoma | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| carboplatin | Drug | Carboplatin | ALIAS |
| etoposide | Drug | Etoposide | ALIAS |
| ifosfamide | Drug | Ifosfamide | ALIAS |
| rituximab | Biological | Rituximab | ALIAS |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 19 Years
- Maximum age
- 120 Years
Show eligibility criteria text
Inclusion Criteria: * Histologically confirmed recurrent or refractory B-cell non-Hodgkin's lymphoma o CD20 positive * Bidimensionally measurable or evaluable disease * 19 years old and over * ECOG 0-2 or Karnofsky 70-100% * Life expectancy at least 3 months * WBC at least 3,000/mm3 * Granulocyte count at least 1,000/mm3 * Platelet count at least 100,000/mm3 * Bilirubin no greater than 1.5 times upper limit of normal(ULN) * AST or ALT no greater than 2.5 times ULN * Creatinine no greater than 1.5 mg/dL * Fertile patients must use effective contraception * Concurrent non-steroidal hormonal therapy allowed for non-disease related conditions (e.g., insulin for diabetes) Exclusion Criteria: * No myelodysplastic syndrome or chronic myeloid leukemia * Not pregnant or nursing/negative pregnancy test * No other prior malignancy except curatively treated basal cell carcinoma, squamous cell carcinoma, or carcinoma in situ of the cervix * No active serious infection * No other concurrent serious medical condition that would preclude study * No prior bone marrow or peripheral blood stem cell transplantation for non-Hodgkin's lymphoma * No other concurrent chemotherapy * No concurrent corticosteroids except transient administration as antiemetic * No concurrent radiotherapy * No other concurrent investigational therapy * No other concurrent antitumor agents
References
Publications (0)
Data not yet available