NCT Number: NCT00344526
Intensive Versus Conventional Treatment in Patients With Primary Amyloidosis
AL amyloidosis is caused by a clonal plasma cell dyscrasia and characterized by progressive deposition of amyloid fibrils derived from monoclonal Ig light chains, leading to multisystem organ failure and death. The prognosis for AL amyloidosis with conventional treatment remains poor, Autologous stem cell transplantation (ASCT) for AL amyloidosis produces high hematologic and organ responses. However, treatment-related mortality remains high and reported series are subject to selection bias.
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Conditions
Age range
18 year–70 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Service des Maladies du Sang, Lille, France
About this study
A prospective randomized trial was conducted to compare in AL amyloidosis ASCT (melphalan 140 or 200 mg/m2 depending on age and clinical status supported with ASCT collected with G-CSF alone) and the oral regimen M-Dex (melphalan 10 mg/m2 and dexamethasone 40 mg for 4 days each months up to 18 months). The objectives were to compare survival and hematologic and clinical responses.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- below 70 years of age
- biopsy proven systemic AL amyloidosis
- no more than 2 prior courses of chemotherapy
- ECOG performance status < 3
- Informed written consent
Exclusion criteria
- localized amyloidosis
- HIV seropositivity
- previous myelodysplasia
- concomitant serious disease
Treatment and study plan
Dexamethasone
DrugAutologous Stem Cell Transplantation
ProcedurePrimary outcomes
-
survival
Secondary outcomes
-
hematologic responses
-
clinical responses
Sponsors and collaborators
Lead sponsor
University Hospital, Limoges
Other
Collaborators
- Ministry of Health, France
Registry information
Official study title
Autologous Stem Cell Transplantation (ASCT) Versus Oral Melphalan and High-Dose Dexamethasone in Patients With AL (Primary)Amyloidosis. A Prospective Randomized Trial .
Important dates
- Study start
- 2000
- Study completion
- 2006
- First posted
- Jun 26, 2006
- Registry last updated
- Jun 28, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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