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Prepublished online as a Blood First Edition Paper on August 21, 2003; DOI 10.1182/blood-2002-10-3263.

Submitted November 1, 2002
Accepted June 27, 2003
Donor CMV serological status and outcome of CMV seropositive recipients after unrelated donor stem cell transplantation; an EBMT Megafile analysis
Per Ljungman*, Ronald Brand, Hermann Einsele, Francesco Frassoni, Dietger Niederwieser, and Catherine Cordonnier
Department of Hematology, Huddinge University Hospital, Stockholm, Sweden
Department of Medical Statistics, Leiden University Medical Center, Leiden, The Netherlands
Department of Medicine, University Hospital, Tuebingen, Germany
Department of Hematology, Ospedale San Martino, Genova, Italy
Department of Hematology/Oncology, University of Leipzig, Leipzig, Germany
Department of Hematology, Hopital Henri Mondor, Creteil, France
* Corresponding author; email: per.ljungman{at}medhs.ki.se.
Rationale: Cytomegalovirus (CMV) has been a major cause of morbidity and mortality after allogeneic stem cell transplantation (SCT). The importance of the recipient's serological status is paramount. However, the importance of the donor's serological status in CMV seropositive recipients is controversial. We analysed the influence of the donor's CMV status in a large cohort of patients. Methods: 7018 CMV seropositive patients reported to the European Group for Blood and Marrow Transplantation were included. 5910 had undergone HLA-identical sibling and 1108 unrelated donor SCT. Univariate and multivariate proportional hazards models were constructed for survival, event free survival, transplant related mortality, and relapse incidence. Findings: Patients receiving grafts from CMV seropositive HLA-identical sibling donors had the same survival as patients grafted from seronegative donors (HR 1.04; p=.37, 95% c.i. [0.95-1.14]). However, unrelated donor SCT recipients receiving grafts from CMV seropositive donors had an improved 5-year survival (35% vs. 27%; HR=0.8; p=.006), an improved event free survival (30% vs. 22%; HR=0.8; p=.01), and a reduced transplant related mortality (49% vs. 62%; HR=0.7; p<.001). There was no influence on the relapse incidence. The effects of donor CMV status remained in multivariate analyses. The effect of donor status was different among different disease categories. In CML patients, T-cell depletion abrogated the beneficial effect of donor status suggesting that the effect is mediated through transfer of donor immunity. Conclusion: Our data suggests that donor CMV status influences outcome of unrelated SCT. For a CMV seropositive patient, a seropositive donor might be preferable.

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