Despite recent advances, allografting remains the only potential cure for myeloma. From July 1999 to June 2005, 100 newly diagnosed patients younger than 65 years were enrolled in a prospective multi-center study. First-line treatment included vincristin, adriamycin and dexamethasone (VAD)-based induction chemotherapy, a cytoreductive autograft (melphalan 200 mg/m2) followed by a single dose of non-myeloablative total body irradiation and allografting from an HLA-identical sibling. Primary endpoints were overall (OS) and event-free (EFS) survivals from diagnosis. After a median follow up of 5 years, OS was not reached and EFS was 37 months. Incidences of acute and chronic graft-vs.-host disease (GHVD) were 38% and 50%, respectively. Complete remission (CR) was achieved in 53% of patients. Profound cytoreduction (CR or very good partial remission) prior to allografting was associated with achievement of post-transplant CR (HR 2.20, p=0.03) and longer EFS (HR 0.33, p<0.01). Conversely, development of chronic GVHD was not correlated with CR or response duration. This tandem transplant approach allows prolonged survival and long-term disease control in patients with reduced tumor burden at the time of allografting. We are currently investigating the role of "new drugs" in intensifying pre-transplant cytoreduction and post-transplant graft-vs.-myeloma effects to further improve clinical outcomes.
Nonmyeloablative allografting for newly diagnosed multiple myeloma: the experience of the Gruppo Italiano Trapianti di Midollo
BRUNO, Benedetto;GIACCONE, Luisa;PALUMBO, Antonio;RICARDI, Umberto;BOCCADORO, Mario
2009-01-01
Abstract
Despite recent advances, allografting remains the only potential cure for myeloma. From July 1999 to June 2005, 100 newly diagnosed patients younger than 65 years were enrolled in a prospective multi-center study. First-line treatment included vincristin, adriamycin and dexamethasone (VAD)-based induction chemotherapy, a cytoreductive autograft (melphalan 200 mg/m2) followed by a single dose of non-myeloablative total body irradiation and allografting from an HLA-identical sibling. Primary endpoints were overall (OS) and event-free (EFS) survivals from diagnosis. After a median follow up of 5 years, OS was not reached and EFS was 37 months. Incidences of acute and chronic graft-vs.-host disease (GHVD) were 38% and 50%, respectively. Complete remission (CR) was achieved in 53% of patients. Profound cytoreduction (CR or very good partial remission) prior to allografting was associated with achievement of post-transplant CR (HR 2.20, p=0.03) and longer EFS (HR 0.33, p<0.01). Conversely, development of chronic GVHD was not correlated with CR or response duration. This tandem transplant approach allows prolonged survival and long-term disease control in patients with reduced tumor burden at the time of allografting. We are currently investigating the role of "new drugs" in intensifying pre-transplant cytoreduction and post-transplant graft-vs.-myeloma effects to further improve clinical outcomes.File | Dimensione | Formato | |
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