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RESEARCH PRODUCT
Impact of cytomegalovirus DNAemia on overall and non-relapse mortality in allogeneic stem cell transplant recipients.
Víctor VinuesaEstela GiménezDavid NavarroEliseo AlbertJuan Carlos Hernández-boludaJosé Luis PiñanaPaula AmatCarlos Solanosubject
AdultMalemedicine.medical_specialtyAdolescentCongenital cytomegalovirus infectionCytomegalovirus030230 surgeryAntiviral Agents03 medical and health sciencesYoung Adult0302 clinical medicineInternal medicinemedicineHumansTransplantation HomologousNonrelapse mortalityCumulative incidenceYoung adultAgedRetrospective StudiesTransplantationbusiness.industryHazard ratiovirus diseasesRetrospective cohort studyMiddle Agedmedicine.diseaseConfidence intervalTransplant RecipientsSurgeryInfectious DiseasesSpainCytomegalovirus InfectionsDNA ViralFemaleStem cellbusiness030215 immunologyStem Cell Transplantationdescription
Background We conducted a retrospective single-center study to investigate the potential impact of cytomegalovirus (CMV) DNAemia on mortality in allogeneic stem cell transplant recipients (allo-SCT). Methods A total of 151 consecutive patients who underwent T-cell replete allo-SCT were included in the study. Patients with CMV DNAemia were treated pre-emptively with antivirals upon detection of plasma CMV DNA loads >1500 IU/mL. Results At least one episode of CMV DNAemia occurred in 109 (72.2%), and 67 of these patients (61.5%) required one or more courses of antiviral therapy. The cumulative incidence of 1-year overall and non-relapse mortality (NRM) was 28.5% (95% confidence interval [CI], 18.4%-39.5%) and 23.2% (95% CI 12.81%-35.4%), respectively. The occurrence of either CMV DNAemia or CMV recurrences had no apparent effect on 1-year overall mortality and NRM; nevertheless, a trend towards an increased risk of death was seen in patients with one or more episodes of CMV DNAemia requiring antiviral therapy (hazard ratio [HR], 2.10; 95% CI, 0.96-4.61; P=0.06 for overall mortality, and HR, 2.36; 95% CI, 0.96-5.76; P=0.06 for NRM) but not in those displaying one or more self-resolving episodes. Conclusion Therefore, the data suggest that withholding pre-emptive antiviral therapy until the plasma CMV DNA load reaches 1500 IU/mL has no apparent detrimental effect on patient survival. This article is protected by copyright. All rights reserved.
year | journal | country | edition | language |
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2017-06-20 | Transplant infectious disease : an official journal of the Transplantation Society |