Epstein-Barr virus (EBV)
viremia is a common complication after allogeneic
hematopoietic stem cell transplantation (allo-HSCT). The purpose of this study was to evaluate the impacts of early-onset EBV
viremia in acute
leukemia (AL) patients who underwent allo-HSCT with
anti-thymocyte globulin (ATG)-containing myeloablative conditioning (
MAC) regimen. Two hundred and ninety-six patients were included between January 2013 and December 2015. In 126 patients (42.6%) who developed early-onset EBV
viremia, with a median time of 48 (range 18~99) days after allo-HSCT. The cumulative incidence of EBV
viremia at 30 and 90 days after allo-HSCT were 4.1 and 39.9%, respectively. Prognostic analysis showed that the adjusted overall survival in early-EBVpos group was significantly lower than early-EBVneg group within the first 26.7 months after allo-HSCT [hazard ratio (HR), 1.63, P = 0.012], but significantly higher than those afterward (after 26.7 months: HR 0.11, P = 0.035); for the adjusted event-free survival, early-EBVpos group was significantly inferior in early-EBVpos group within the first 10.8 months after
transplantation (HR: 1.55, P = 0.042), and this adverse effect was not detected any more after 10.8 months (HR: 0.58, P = 0.107). Compared with early-EBVneg group after adjusting by aGVHD and CMV
viremia, HR for death from transplant-related mortality was 2.78-fold higher in patients with early-EBV
viremia in piecewise constant Cox analysis (P = 0.006), and this adverse effect was not detected any more after the cut-point time (HR: 0.67, P = 0.361). No differences in terms of relapse and relapse mortality were observed between early-EBVpos and early-EBVneg group (P > 0.05). In conclusion, the impacts on transplant outcomes of early-EBV
viremia were time-dependent, which may help to optimize management strategies for early-EBV
viremia after allo-HSCT, especially in AL patients with ATG-containing
MAC regimen.