Journal of Clinical Oncology, Vol 15, 557-565, Copyright © 1997 by American Society of Clinical Oncology
Unrelated donor bone marrow transplantation for children with acute leukemia
SM Davies, JE Wagner, XO Shu, BR Blazar, E Katsanis, PJ Orchard, JH Kersey, KE Dusenbery, DJ Weisdorf, PB McGlave and NK Ramsay
Department of Pediatrics, University of Minnesota, Minneapolis 55455, USA. davie008@maroon.tc.umn.edu
PURPOSE: To test the use of unrelated donor bone marrow transplantation
(URD BMT) to cure children with high-risk acute leukemias. PATIENTS AND
METHODS: Between June 1985 and December 1994, 50 children with acute
leukemia (15 acute myelogenous leukemia [AML], 35 acute lymphoblastic
leukemia [ALL]; 22 greater than second complete remission [CR]) received
BMT from a URD at the University of Minnesota. Ages ranged from 0.9 to 17.5
years (median, 8.8). Median follow-up is 2.1 years (range, 1 to 7.3).
Thirty patients (60%) received bone marrow fully matched at HLA-A,B and
DRB1; 20 (40%) received bone marrow with a major or minor mismatch at a
single HLA-A or B locus. RESULTS: The median time to neutrophil engraftment
was day 24 (range, 14 to 42 days) in those receiving matched and day 25
(range, 15 to 32 days) in those receiving mismatched marrow (P = .35). The
incidence of grades III to IV graft-versus-host disease (GVHD) was 23% (95%
confidence interval [CI], 7% to 39%) in matched and 32% (95% CI, 8% to 52%)
in HLA- mismatched patients (P = .57). The incidence of chronic GVHD was
50% (95% CI, 28% to 72%) in matched and 57% (95% CI, 23% to 91%) in
mismatched patients (P = .80). Disease-free survival for patients with ALL
is 37% (95% CI, 21% to 53%) at 1 year and 30% (95% CI, 15% to 46%) at 2
years; for patients with AML, 53% (95% CI, 28% to 78%) at 1 year and 33%
(95% CI, 6% to 60%) at 2 years. CONCLUSION: URD BMT is an effective
treatment for children with poor-prognosis acute leukemia and should be
considered for all high-risk patients. Early referral of patients is
strongly recommended.
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