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Clinical Trial Summary

The protocol aims at reducing transplant toxicity and mortality in patients with multiple myeloma.


Clinical Trial Description

Primary end points are engraftment and non-relapse mortality. Secondary end points are disease response, overall survival, progression and event free survivals. Patient eligibility criteria.

Inclusion criteria included:

- Diagnosis of Durie-Salmon stage IIA-IIIB multiple myeloma

- Age > 18 and ≤ 65 years at the start of the donor search

- Presence of concurrent co-morbidities precluding myeloablative conditioning or refusal to undergo a conventional allogeneic transplant

- Capacity to give informed consent

Exclusion criteria included:

- Age > 65 years

- Karnofsky performance status score < 60%

- Progressive disease or stable disease for less than three months

- Central nervous system (CNS) involvement

- Left ventricular ejection fraction < 35% or symptomatic heart failure

- Poorly controlled hypertension

- Pulmonary dysfunction with diffusing capacity for carbon monoxide (DLCO) < 40% and/or need for continuous oxygen supplementation

- Abnormal liver disease with a serum bilirubin greater than twice normal or SGOT and/or SGPT greater than four times the upper limits of normal

- HIV positive patients

- Pregnancy

- Refusal to use contraceptive techniques during and for 12 months following treatment

Informed consent is obtained during study registration from each patient according to the Institutional Review Boards of the participating centers. The study is conducted according to the Declaration of Helsinki. ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00327314
Study type Interventional
Source Azienda Ospedaliera San Giovanni Battista
Contact Benedetto Bruno, MD, PhD
Phone +39-011-6334419
Email benedetto.bruno@unito.it
Status Recruiting
Phase Phase 2
Start date December 2002
Completion date October 2006

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