Features of Cytomegalovirus DNAemia Blips in Allogeneic Hematopoietic Stem Cell Transplant Recipients: Implications for Optimization of Preemptive Antiviral Therapy Strategies.


Journal

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
ISSN: 1523-6536
Titre abrégé: Biol Blood Marrow Transplant
Pays: United States
ID NLM: 9600628

Informations de publication

Date de publication:
05 2020
Historique:
received: 18 11 2019
revised: 15 01 2020
accepted: 22 01 2020
pubmed: 3 2 2020
medline: 24 6 2021
entrez: 3 2 2020
Statut: ppublish

Résumé

Cytomegalovirus (CMV) DNAemia occurs frequently in allogeneic hematopoietic stem cell transplant recipients (allo-HSCT). There is limited information about the incidence, features, and clinical impact of CMV DNAemia blips (episodes defined by an isolated positive PCR result) in this setting. In this retrospective study, 225 consecutive adult patients undergoing any modality of allo-HSCT at our center between May 2012 and July 2019 were included. Plasma CMV DNA load was monitored using a highly sensitive real-time PCR assay. In all, 187 of 225 patients had CMV DNAemia through day 365 after allo-HSCT (total number of episodes, n = 379). Eighty-three of the 187 patients had 1 or more blips (n = 104). Blips occurred as a first episode of CMV DNAemia as opposed to prolonged CMV DNAemia (≥2 consecutive positive PCR results) in 47 patients; in 20 of these patients, blips represented the only documented episode throughout the study period, and in 27 patients, blips preceded a prolonged CMV DNAemia episode. In the remaining 36 patients, blips developed as recurrences. Blips presenting as initial episodes occurred more frequently (P < .001) in patients receiving an allograft from a CMV-seropositive donor. The cumulative incidence of recurrent CMV DNAemia following initial blips, self-resolving prolonged CMV DNAemia episodes, or CMV DNAemia episodes treated preemptively with antivirals was not significantly different (P = .34). Receiver operating characteristic curve analysis indicated that a CMV DNA load cutoff of 48 IU/mL yielded the highest combined sensitivity (66%) and specificity (70.2%) for predicting a prolonged CMV DNAemia episode. The practical implications of our data in the optimization of preemptive antiviral therapy strategies are discussed.

Identifiants

pubmed: 32007638
pii: S1083-8791(20)30047-1
doi: 10.1016/j.bbmt.2020.01.015
pii:
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

972-977

Informations de copyright

Copyright © 2020 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Dixie Huntley (D)

Microbiology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.

Alberto Talaya (A)

Microbiology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.

Estela Giménez (E)

Microbiology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.

Ariadna Martínez (A)

Hematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.

Juan Carlos Hernández-Boluda (JC)

Hematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain; Department of Medicine, School of Medicine, University of Valencia, Valencia, Spain.

Rafael Hernani (R)

Hematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.

Ignacio Torres (I)

Microbiology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.

Juan Alberola (J)

Department of Microbiology, School of Medicine, University of Valencia, Valencia, Spain.

Eliseo Albert (E)

Microbiology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.

José Luis Piñana (JL)

Hematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.

Carlos Solano (C)

Hematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain; Department of Medicine, School of Medicine, University of Valencia, Valencia, Spain.

David Navarro (D)

Microbiology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain; Department of Microbiology, School of Medicine, University of Valencia, Valencia, Spain. Electronic address: david.navarro@uv.es.

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Classifications MeSH