Clinical Trials Directory

Trials / Completed

CompletedNCT00002810

High-Dose Melphalan Followed by Peripheral Stem Cell Transplant in Treating Patients With Amyloidosis

Autologous Peripheral Blood Stem Cell Transplantation With High Dose Melphalan For Treatment Of Primary Amyloidosis (AL)

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
Sponsor
Temple University · Academic / Other
Sex
All
Age
16 Years – 65 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of plasma cells, either by killing the cells or by stopping them from dividing. Having a peripheral stem cell transplant to replace the blood-forming cells destroyed by chemotherapy, allows higher doses of chemotherapy to be given so that more plasma cells are killed. By reducing the number of plasma cells, the disease may progress more slowly. PURPOSE: This phase II trial is studying how well giving high-dose melphalan together with peripheral stem cell transplant works in treating patients with primary amyloidosis or amyloidosis associated with multiple myeloma.

Detailed description

OBJECTIVES: * Assess overall and progression-free survival following high-dose melphalan and autologous peripheral blood stem cell transplantation in patients with primary amyloidosis. * Evaluate the toxic effects associated with this treatment regimen. * Evaluate the function of involved organs, especially the heart, lungs, and nervous system, before and after treatment with this regimen. OUTLINE: Peripheral blood stem cells (PBSC) are mobilized with granulocyte colony-stimulating factor (G-CSF) for 5 days and then collected by leukapheresis. Patients receive high-dose melphalan on 2 consecutive days, followed by 1 day of rest, then by PBSC transplantation. G-CSF is given from 1 day after transplantation until the neutrophil count is greater than 1,500 for 3 consecutive days. Patients are followed at 100 days and 1 year post-transplant. PROJECTED ACCRUAL: A very small number of patients are expected to be accrued over 5-10 years.

Conditions

Interventions

TypeNameDescription
BIOLOGICALfilgrastim
DRUGmelphalan
PROCEDUREbone marrow ablation with stem cell support
PROCEDUREperipheral blood stem cell transplantation

Timeline

Start date
1996-05-01
Primary completion
2006-05-01
Completion
2006-05-01
First posted
2003-01-27
Last updated
2010-10-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00002810. Inclusion in this directory is not an endorsement.