Trials / Unknown
UnknownNCT00384553
Risk Adapted Therapy Optimization for Patients With Relapsed or Refractory Aggressive Non-Hodgkin-Lymphoma
- Status
- Unknown
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 30 (planned)
- Sponsor
- University of Magdeburg · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
This study investigates toxicity and efficacy of 2 x R-DHAP followed by High dose chemotherapy R-TEC and autologous stem cell transplantation in patients with relapsed or refractory aggressive Non- Hodgkins's Lymphoma.
Detailed description
Initial Cytoreduction is performed with DHAP- protocol using dexamethasone, cytarabine and cisplatin followed by high dose chemotherapy with treosulfan, etoposide and cisplatin (TEC) an autologous peripheral blood stem cell transplantation(aPBSCT). In case of only partial remission a second identical high dose chemotherapy and aPBSCT follows. Patients with primary refractory disease or early relapse within 6 months should receive a allogenous stem cell transplantation. For Patients with CD 20 positive B-cell lymphoma the chemotherapy regiments DHAP and TEC are combined with rituximab.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Rituximab | |
| DRUG | DHAP | |
| DRUG | TEC | |
| DRUG | autologous stem cell transplantation |
Timeline
- Start date
- 2004-06-01
- Completion
- 2010-06-01
- First posted
- 2006-10-06
- Last updated
- 2006-10-06
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT00384553. Inclusion in this directory is not an endorsement.