Incidence of CMV Replication and the Role of Letermovir Primary/Secondary Prophylaxis in the Early Phase After Allogeneic Hematopoietic Stem Cell Transplantation - A Single Centre Study.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 14 08 2020
revised: 27 08 2020
accepted: 28 08 2020
entrez: 29 9 2020
pubmed: 30 9 2020
medline: 8 10 2020
Statut: ppublish

Résumé

Cytomegalovirus (CMV) replication may cause life-threatening complications after allogeneic haematopoietic stem cell transplantation (allo-HSCT). The aim of the study was to characterize CMV events, and the outcome of letermovir (LTV) CMV prophylaxis. In this retrospective analysis of patients treated with an allo-HSCT between 2010 and 2020, we determined plasma CMV events, as well as associated risk factors. We identified 423 patients who had undergone allo-HSCT between 2010 and 2020. CMV DNAemia was found in 130/423 (30.7%) of patients. CMV reactivation rate was significantly higher in patients with acute graft-versus-host disease, HLA mismatch, and CMV IgG seropositivity of donors and recipients. Among 42 patients receiving LTV prophylaxis those, 5 (11.9%) showed CMV DNAemia under LTV versus 87/353 (24.6%) in a control group. Despite the development of better approaches with weekly monitoring and early treatment initiation, CMV reactivations play an important role after allo-HSCT.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Cytomegalovirus (CMV) replication may cause life-threatening complications after allogeneic haematopoietic stem cell transplantation (allo-HSCT). The aim of the study was to characterize CMV events, and the outcome of letermovir (LTV) CMV prophylaxis.
PATIENTS AND METHODS METHODS
In this retrospective analysis of patients treated with an allo-HSCT between 2010 and 2020, we determined plasma CMV events, as well as associated risk factors.
RESULTS RESULTS
We identified 423 patients who had undergone allo-HSCT between 2010 and 2020. CMV DNAemia was found in 130/423 (30.7%) of patients. CMV reactivation rate was significantly higher in patients with acute graft-versus-host disease, HLA mismatch, and CMV IgG seropositivity of donors and recipients. Among 42 patients receiving LTV prophylaxis those, 5 (11.9%) showed CMV DNAemia under LTV versus 87/353 (24.6%) in a control group.
CONCLUSION CONCLUSIONS
Despite the development of better approaches with weekly monitoring and early treatment initiation, CMV reactivations play an important role after allo-HSCT.

Identifiants

pubmed: 32988922
pii: 40/10/5909
doi: 10.21873/anticanres.14611
doi:

Substances chimiques

Acetates 0
Quinazolines 0
letermovir 1H09Y5WO1F

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5909-5917

Informations de copyright

Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Ursina Studer (U)

Division of Hematology, University Hospital Basel, Basel, Switzerland.

Nina Khanna (N)

Division of Infectious Diseases and Hospital Epidemiology, University Hospital Basel, Basel, Switzerland.

Karoline Leuzinger (K)

Clinical Virology, Laboratory Medicine, University Hospital Basel, Basel, Switzerland.
Transplantation and Clinical Virology, Department of Biomedicine, University of Basel, Basel, Switzerland.

Hans H Hirsch (HH)

Division of Infectious Diseases and Hospital Epidemiology, University Hospital Basel, Basel, Switzerland.
Clinical Virology, Laboratory Medicine, University Hospital Basel, Basel, Switzerland.
Transplantation and Clinical Virology, Department of Biomedicine, University of Basel, Basel, Switzerland.

Dominik Heim (D)

Division of Hematology, University Hospital Basel, Basel, Switzerland.

Claudia Lengerke (C)

Division of Hematology, University Hospital Basel, Basel, Switzerland.

Dimitrios A Tsakiris (DA)

Division of Hematology, University Hospital Basel, Basel, Switzerland.

Joerg Halter (J)

Division of Hematology, University Hospital Basel, Basel, Switzerland.

Sabine Gerull (S)

Division of Hematology, University Hospital Basel, Basel, Switzerland.

Jakob Passweg (J)

Division of Hematology, University Hospital Basel, Basel, Switzerland.

Michael Medinger (M)

Division of Hematology, University Hospital Basel, Basel, Switzerland michael.medinger@usb.ch.
Division of Internal Medicine, Department of Medicine, University Hospital Basel, Basel, Switzerland.

Malena Gwerder (M)

Division of Hematology, University Hospital Basel, Basel, Switzerland.

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Classifications MeSH