Fludarabine Added to Induction Treatment in Untreated Multiple Myeloma Patients

Nordic Myeloma Study Group

Status and phase

Unknown

Phase 2

Conditions

Multiple Myeloma

Treatments

Drug: Fludarabine

Study type

Interventional

Funder types

Other

Identifiers

NCT00382694

NMSG#13/03

Details and patient eligibility

About

Multiple myeloma is an incurable malignant disease which evnetuelly will relapse after primary treatment. Clonal B-cells have been identified and in theory these cells might be sleeping during primary treatment and be responsible for later relapse. Fluarabine has documented effect on both resting and dividing cells including B-cells. The protocol aim at evaluating safety and toxicity of adding fludarabine to induction chemotherapy with cyclophosphamide and dexamethasone before high-dose melphalan with autologous stem cell support.

Full description

This is a randomised, placebo controlled, phase II study evaluating toxicity and safety of fludarabine added to CyDex (cyclophosphamide+dexamethasone) as induction therapy in younger patients with untreated and treatment demanding multiple myeloma. The treatment regimen Patients will be randomised at diagnosis either to CyDex + Placebo (control Arm A) or CyDex + Fludarabine (Experimental Arm B).

OBJECTIVES:

Primary:To determine the toxicity and safety of fludarabine when added to induction therapy by registration of side effects and adverse events in accordance with the common toxicity criteria (CTC).
Secondary:To quantitate clonal cells in bone marrow and blood by flow cytometry (MRD)and to study new potential prognostic markers identified by cytomic, genomic and proteomic analysis.
Tertiary: To estimate the efficacy of fludarabine when added to induction chemotherapy(CyDex) in patients with multiple myeloma by clinical end points: disease response and progression free survival.

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Multiple myeloma, stage I-III, previously untreated, and eligible for induction therapy followed by high dose treatment supported by autologous stem cell transplantation.

Exclusion criteria

Severe uncontrolled clinical or microbiological evidence of infection at the time of enrolment.
Other active malignancy.
Severe coincident heart or lung disease including uncontrolled hypertension, unstable angina, congestive heart failure, coronary angioplasty within six months, myocardial infarction within the last six months, or uncontrolled cardiac arrhythmia.
Other severe illness including poorly controlled diabetes.
Haemolytic anaemia (Coombs positive without evidence of haemolysis is accepted).
Idiopathic thrombocytopenic purpura.
Terminal illness.
Allogenic transplantation planned within 6 months.
Chemotherapy before inclusion.
Pregnancy or breast-feeding, or inadequate contraceptive precautions.
Psychiatric disease, abuse of alcohol or narcotics, or any other disorder that might compromise the patients ability to give informed consent.