Clinical Trials Directory

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

TypeNameDescription
DRUGRituximab
DRUGDHAP
DRUGTEC
DRUGautologous 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.