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Blood, 15 May 2001, Vol. 97, No. 10, pp. 2957-2961
CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS
Survival after transplantation of unrelated donor umbilical cord
blood is comparable to that of human leukocyte antigen-matched
unrelated donor bone marrow: results of a
matched-pair analysis
Juliet N. Barker,
Stella M. Davies,
Todd DeFor,
Norma K. C. Ramsay,
Daniel J. Weisdorf, and
John E. Wagner
From the Blood and Marrow Transplant Program,
Department of Medicine, and Department of Pediatrics, University of
Minnesota School of Medicine, Minneapolis, MN.
Umbilical cord blood (UCB) is being increasingly used for
hematopoietic stem cell transplantation and has been associated with a
reduced incidence of severe graft-versus-host disease (GVHD). To
further investigate the relative merits of unrelated donor UCB versus
bone marrow (BM), a matched-pair analysis comparing the outcomes of
recipients of 0 to 3 human leukocyte antigen (HLA)-mismatched UCB and
HLA-A, B, DRB1-matched BM was performed. UCB patients, who received
cyclosporine (CSA) and methylprednisolone (MP), were matched for age,
diagnosis, and disease stage with BM patients, who received either
methotrexate (MTX) and CSA (26 pairs) or T-cell depletion (TCD) and
CSA/MP (31 pairs). Patients were predominantly children (median age, 5 years) undergoing transplantation for malignancy, storage diseases, BM
failure, and immunodeficiency syndromes between 1991 and 1999. Although
neutrophil recovery was significantly slower after UCB transplantation,
the probability of donor-derived engraftment at day 45 was 88% in UCB
versus 96% in BM-MTX recipients (P = .41) and 85% in
UCB versus 90% in BM-TCD recipients (P = .32),
respectively. Platelet recovery was similar in UCB versus BM pairs.
Furthermore, incidences of acute and chronic GVHD were similar in UCB
and BM recipients, with 53% of UCB versus 41% of BM-MTX recipients
alive (P = .40) and 52% of UCB versus 56% of BM-TCD
recipients alive at 2 years (P > .80), respectively. These data suggest that despite increased HLA disparity, probabilities of engraftment, GVHD, and survival after UCB transplantation are comparable to those observed after HLA-matched BM transplantation. Therefore, UCB should be considered an acceptable alternative to
HLA-matched BM for pediatric patients.

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