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Allogeneic bone marrow transplantation for chronic myeloid leukemia in childhood: a report from the Société Française de Greffe de Moelle et de Thérapie Cellulaire (SFGM-TC)

Authors :
Kuenz M
Frédéric Millot
Pierre Bordigoni
Emmanuel Plouvier
Rome A
Mauricette Michallet
François Guilhot
G. Michel
Joelle Guilhot
Frédéric Garban
Helene Esperou
Bourhis Jl
Didier Blaise
J.-H. Dalle
Source :
Bone Marrow Transplantation. 32:993-999
Publication Year :
2003
Publisher :
Springer Science and Business Media LLC, 2003.

Abstract

To determine the results of allogeneic hematopoietic stem cell (HSC) transplantation for chronic myelogenous leukemia (CML) at various stages of the disease in children, a retrospective analysis was carried out on the outcome of transplants performed on 76 children and teenagers with CML between 1982 and 1998. In all, 60 patients were transplanted from a matched sibling donor (MSD) and 16 from a matched unrelated donor (MUD). There was a higher incidence of acute graft-versus-host disease after MUD transplantation (P10(-3)). The main cause of death was transplant-related toxicity in both groups. In MSD recipients, the probability of relapse at 5 years for patients transplanted in the first chronic phase was lower than in patients transplanted in the advanced phase (relative risk (rr)=5.90; 95% confidence interval (CI), 1.85-18.82, P0.01). The estimated 5-year event-free survival (EFS) rate was higher after MSD vs MUD transplantation (61% (95% CI, 48-73%) vs 27% (95% CI, 4-49%), rr=0.25, P10(-3)). In children transplanted from MSD, the 5-year EFS was higher when transplantation was performed in the first chronic phase vs the advanced phases (73% (95% CI, 59-87%) vs 32% (95% CI, 10-54%), P10(-3)). Disease status at transplantation was the unique factor influencing survival in patients undergoing transplantation from MSD with a better outcome for those transplanted in the first chronic phase. Allogeneic HSC offers a possibility of curing childhood CML with a significant advantage for patients transplanted in chronic phase using a human leukocyte antigen-identical sibling donor.

Details

ISSN :
14765365 and 02683369
Volume :
32
Database :
OpenAIRE
Journal :
Bone Marrow Transplantation
Accession number :
edsair.doi.dedup.....3fea55f2764d38af9984a329f19f8ab7