Clinical Trials Directory

Trials / Terminated

TerminatedNCT00005787

Peripheral Stem Cell Transplantation to Prevent Neutropenia in Patients Receiving Chemotherapy for Relapsed or Refractory Non-Hodgkin's Lymphoma

Ex Vivo Expanded Peripheral Blood Mononuclear Cells for the Elimination of Neutropenia Associated With High Dose Chemotherapy

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
3 (actual)
Sponsor
Northwestern University · Academic / Other
Sex
All
Age
17 Years – 65 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Peripheral stem cell transplantation may be able to replace immune cells that were destroyed by chemotherapy used to kill cancer cells. Treating the peripheral stem cells in the laboratory may improve the effectiveness of the transplant. PURPOSE: Phase I trial to study the effectiveness of peripheral stem cell transplantation in patients who have relapsed or refractory non-Hodgkin's lymphoma and who will be treated with high-dose chemotherapy.

Detailed description

OBJECTIVES: * Determine the toxicity of ex vivo expanded peripheral blood mononuclear cells (EVE PBMNC) as a supplement to high-dose chemotherapy and conventional autograft in patients with relapsed or refractory non-Hodgkin's lymphoma. * Compare the effect of EVE PBMNC on white blood cell, red blood cell, and platelet recovery in patients on this study vs historical controls, matched by protocol, disease status, and prior therapy. * Determine the optimal duration of culture and time of harvest for the production of neutrophils in vivo. * Determine the relationships between length of culture, immunophenotype, and clinical outcome. * Determine the required numbers of white blood cell precursors for clinical efficacy. * Assess the need for multiple transfusions of EVE PBMNC during the post-transplantation period. OUTLINE: Autologous peripheral blood mononuclear cells (PBMNC) are harvested. Unselected PBMNC are cultured and expanded ex vivo in flt3 ligand, interleukin-3, filgrastim (G-CSF), sargramostim (GM-CSF), and epoetin alfa for 13 days. Expanded PBMNC are reinfused on day 0. Patients are followed monthly for 1 year. PROJECTED ACCRUAL: A total of 24 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
BIOLOGICALepoetin alfa
BIOLOGICALfilgrastim
BIOLOGICALrecombinant flt3 ligand
BIOLOGICALrecombinant interleukin-3
BIOLOGICALsargramostim
PROCEDUREin vitro-treated peripheral blood stem cell transplantation

Timeline

Start date
1999-09-01
Primary completion
2002-01-01
Completion
2002-01-01
First posted
2003-01-27
Last updated
2012-06-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00005787. Inclusion in this directory is not an endorsement.