Early human cytomegalovirus replication after transplantation is associated with a decreased relapse risk: evidence for a putative virus-versus-leukemia effect in acute myeloid leukemia patients

Ahmet Elmaağaclı(West Cancer Center), Nina K. Steckel(West Cancer Center), Michael Koldehoff(West Cancer Center), Yael Hegerfeldt(West Cancer Center), Rudolf Trenschel(West Cancer Center), Markus Ditschkowski(West Cancer Center), Sandra Christoph(West Cancer Center), Tanja Gromke(West Cancer Center), Lambros Kordelas(West Cancer Center), Hellmut Ottinger(West Cancer Center), Rudolf Stefan Ross(Institute of Virology of the Slovak Academy of Sciences), Peter A. Horn(University of Duisburg-Essen), Susanne Schnittger(Munich Leukemia Laboratory (Germany)), Dietrich W. Beelen(West Cancer Center)
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Abstract

The impact of early human cytomegalovirus (HCMV) replication on leukemic recurrence was evaluated in 266 consecutive adult (median age, 47 years; range, 18-73 years) acute myeloid leukemia patients, who underwent allogeneic stem cell transplantation (alloSCT) from 10 of 10 high-resolution human leukocyte Ag-identical unrelated (n = 148) or sibling (n = 118) donors. A total of 63% of patients (n = 167) were at risk for HCMV reactivation by patient and donor pretransplantation HCMV serostatus. In 77 patients, first HCMV replication as detected by pp65-antigenemia assay developed at a median of 46 days (range, 25-108 days) after alloSCT. Taking all relevant competing risk factors into account, the cumulative incidence of hematologic relapse at 10 years after alloSCT was 42% (95% confidence interval [CI], 35%-51%) in patients without opposed to 9% (95% CI, 4%-19%) in patients with early pp65-antigenemia (P < .0001). A substantial and independent reduction of the relapse risk associated with early HCMV replication was confirmed by multivariate analysis using time-dependent covariate functions for grades II to IV acute and chronic graft-versus-host disease, and pp65-antigenemia (hazard ratio = 0.2; 95% CI, 0.1-0.4, P < .0001). This is the first report that demonstrates an independent and substantial reduction of the leukemic relapse risk after early replicative HCMV infection in a homogeneous population of adult acute myeloid leukemia patients.


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