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Prepublished online as a Blood First Edition Paper on June 7, 2002; DOI 10.1182/blood-2002-01-0294.
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Blood, 1 September 2002, Vol. 100, No. 5, pp. 1611-1618
CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS
Transplantation of unrelated donor umbilical cord blood in 102 patients with malignant and nonmalignant diseases: influence of CD34
cell dose and HLA disparity on treatment-related mortality and
survival
John E. Wagner,
Juliet N. Barker,
Todd E. DeFor,
K. Scott Baker,
Bruce R. Blazar,
Cindy Eide,
Anne Goldman,
John Kersey,
William Krivit,
Margaret L. MacMillan,
Paul J. Orchard,
Charles Peters,
Daniel J. Weisdorf,
Norma K. C. Ramsay, and
Stella M. Davies
From the Blood and Marrow Transplant Program of the
Departments of Pediatrics and Medicine and the Biostatistical Support
Group, University of Minnesota Cancer Center and School of Medicine,
Minneapolis.
The potential benefits of unrelated donor marrow
transplantation are offset by the immunologic complications of
graft-versus-host disease (GVHD) and infection. Therefore, we used
cryopreserved umbilical cord blood (UCB) as a strategy to reduce the
risks of GVHD and treatment-related mortality (TRM) and improve
survival. Data on 102 patients (median age 7.4 years) who received
transplants between 1994 and 2001 for the treatment of malignant
(n = 65; 68% were high-risk patients) and nonmalignant (n = 37) diseases were evaluated. Log-rank tests and Cox regression analyses
were used to determine the effects of various demographic,
graft-related, and treatment factors on engraftment, GVHD, TRM,
relapse, and survival. As of October 15, 2001, the median follow-up was
2.7 years (range, 0.3-7.2). Incidences of neutrophil and platelet engraftment were 0.88 (CI, 0.81-0.95) and 0.65 (CI, 0.53-0.77), respectively. Notably, incidences of severe acute and chronic GVHD were
0.11 (CI, 0.05-0.17) and 0.10 (CI, 0.04-0.16), respectively. At 1 year
after transplantation, proportions of TRM and survival were 0.30 (CI,
0.21-0.39) and 0.58 (CI, 0.48-0.68), respectively. In Cox regression
analyses, CD34 cell dose was the one factor consistently identified as
significantly associated with rate of engraftment, TRM, and survival.
Despite the low incidence of GVHD, the proportion of patients with
leukemia relapse at 2 years was 0.17 (CI, 0.00-0.38) and 0.45 (CI,
0.28-0.61) for patients with standard and high-risk disease,
respectively. There is a high probability of survival in recipients of
UCB grafts that are disparate in no more than 2 human leukocyte
antigens (HLAs) when the grafts contain at least
1.7 × 105 CD34+ cells per kilogram of
recipient's body weight. Therefore, graft selection should be based
principally on CD34 cell dose when multiple UCB units exist with an HLA
disparity of 2 or less.

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