Epstein-Barr virus DNA load kinetics analysis in allogeneic hematopoietic stem cell transplant recipients: Is it of any clinical usefulness?

•The initial plasma EBV DNA load is not predictive of either high-level EBV viremia or PTLD.•The plasma EBV DNA load doubling time does not allow prediction of eitherhigh-level EBV viremia or PTLD.•The plasma EBV DNA half-life in initial episodes of EBV DNAemia is not associated with recurrences.•Ba...

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Veröffentlicht in:Journal of clinical virology 2017-12, Vol.97, p.26-32
Hauptverfasser: Solano, Carlos, Mateo, Eva María, Pérez, Ariadna, Talaya, Alberto, Terol, María José, Albert, Eliseo, Giménez, Estela, Vinuesa, Víctor, Piñana, José Luis, Boluda, Juan Carlos Hernández, Navarro, David
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Sprache:eng
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Zusammenfassung:•The initial plasma EBV DNA load is not predictive of either high-level EBV viremia or PTLD.•The plasma EBV DNA load doubling time does not allow prediction of eitherhigh-level EBV viremia or PTLD.•The plasma EBV DNA half-life in initial episodes of EBV DNAemia is not associated with recurrences.•Baseline transplant conditions have no impact on plasma EBV DNA load doubling times or half-lifes. There is a lack of clinical information regarding the usefulness of plasma Epstein-Barr virus (EBV) DNA load kinetics analyses in the management of EBV infections in allogeneic hematopoietic stem cell transplantation (allo-HSCT) recipients. Namely, it remains unknown whether this type of analysis can help physicians to anticipate the development of high-level EBV DNAemia episodes requiring rituximab treatment or predict the risk of recurrent EBV DNAemia or post-transplant lymphoproliferative disorders (PTLDs). Unicentric, retrospective, observational study including 142 consecutive patients undergoing T-cell replete allo-HSCT. The plasma EBV DNA load was monitored on a weekly basis using the artus® EBV PCR kit. Fifty-five of the 142 patients (38.7%) developed at least one episode of EBV DNAemia; 13 of the 55 initial EBV DNAemia episodes (23.6%) were preemptively treated with rituximab, 7 patients had a recurrent episode of EBV DNAemia, and biopsy-proven PTLDs were diagnosed in 4 patients. The initial plasma EBV DNA load was not significantly different (P=0.269) in episodes of self-resolving EBV DNAemia, those requiring rituximab treatment, or those leading to PTLDs. The plasma EBV DNA load doubling times were similar across all the groups (P=0.799), and the EBV DNA-load half-life was not associated with the occurrence of recurrent EBV DNAemia (P=0.550). Plasma EBV DNA-load kinetics analyses are unlikely to be useful in predicting the occurrence of high-level EBV DNAemia, PTLD, or recurrent EBV DNAemia.
ISSN:1386-6532
1873-5967
DOI:10.1016/j.jcv.2017.10.016