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Lenalidomide plus donor-lymphocytes infusion after allogeneic stem-cell transplantation with reduced-intensity conditioning in patients with high-risk multiple myeloma

Authors :
Didier Blaise
Claude Lemarie
Luca Castagna
Anne-Marie Stoppa
Segolene Duran
Christian Chabannon
Roberto Crocchiolo
Catherine Faucher
Patrick Ladaique
Sabine Furst
Claire Oudin
Boris Calmels
Jean El-Cheikh
Angela Granata
Jean Marc Schiano De Colella
Source :
Experimental Hematology. 40:521-527
Publication Year :
2012
Publisher :
Elsevier BV, 2012.

Abstract

Myeloma relapse is the main cause of death after allogeneic stem cell transplantation. The aim of our observational study was to evaluate the anti-myeloma effect of lenalidomide followed by donor-lymphocyte infusion (DLI) as post-transplantation adoptive immunotherapy. Twelve patients with refractory myeloma were analyzed. The median age at transplantation was 56 years (range, 46-64 years). All patients received reduced-intensity conditioning. Patients were included if progressive or residual disease was observed at day +100 and if no signs of graft-vs-host disease were evident. DLIs were administered after two cycles of lenalidomide. Median dose of lenalidomide was 15 mg (range, 10-25 mg). Patients received a median of six cycles (range, 1-10 cycles). Nine patients (60%) received an escalating dose of DLI. The 1 and 2-year probability of progression-free survival was 75% and 50%, and overall survival was 83% and 69%, respectively. Median overall survival was not reached and median progression-free survival was 23 months. Lenalidomide is well tolerated after allogeneic stem cell transplantation; the combination with DLI did not cause a higher risk of graft-vs-host disease; an immunological synergistic effect was probably present with this strategy. This combination should be evaluated further in a larger cohort of patients.

Details

ISSN :
0301472X
Volume :
40
Database :
OpenAIRE
Journal :
Experimental Hematology
Accession number :
edsair.doi.dedup.....e557054f5e8107ccfc4828be78c6532c
Full Text :
https://doi.org/10.1016/j.exphem.2012.02.009