Letermovir Prophylaxis for CMV Reactivation in Allogeneic Stem Cell Recipients: A Retrospective Single Center Analysis.


Journal

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

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 15 08 2022
revised: 31 08 2022
accepted: 05 09 2022
entrez: 26 10 2022
pubmed: 27 10 2022
medline: 29 10 2022
Statut: ppublish

Résumé

Cytomegalovirus (CMV) reactivation is one of the most clinically significant complications in allogeneic stem cell recipients and a frequent cause for transplantation related mortality. Letermovir is a newly available and recently approved drug for CMV prophylaxis. In a retrospective single center analysis, we investigated the benefit of letermovir as CMV prophylaxis in allogeneic stem cell recipients. We included 48 CMV-seropositive transplant recipients from January 2017 to August 2020 from our department. We compared the rate of CMV reactivation in patients who received letermovir as prophylaxis from day 0 after allogeneic stem cell transplantation (alloSCT) with a control group that did not receive CMV prophylaxis. The primary endpoint was CMV reactivation and was defined as an increase of CMV copies over 1250 Ul/ml in the peripheral blood; secondary endpoints were overall survival (OS) up to 180 days, engraftment and all-cause mortality. We included 21 patients in the control group and 27 patients in the letermovir group. Letermovir treatment led to a significantly reduced incidence of CMV reactivation after alloSCT (33.3% in the letermovir group versus 76.2% in the control group, p<0.001). The OS at day 180 was 80.9% in the control group versus 92.6% in the letermovir group (p<0.05). The median duration of letermovir prophylaxis was 192±104 days. Our results indicate that letermovir prophylaxis is associated with a significant lower risk of CMV reactivation and improved overall survival in CMV-seropositive stem cell recipients. Moreover, a prolonged use of letermovir prophylaxis might be a survival benefit.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Cytomegalovirus (CMV) reactivation is one of the most clinically significant complications in allogeneic stem cell recipients and a frequent cause for transplantation related mortality. Letermovir is a newly available and recently approved drug for CMV prophylaxis. In a retrospective single center analysis, we investigated the benefit of letermovir as CMV prophylaxis in allogeneic stem cell recipients.
PATIENTS AND METHODS METHODS
We included 48 CMV-seropositive transplant recipients from January 2017 to August 2020 from our department. We compared the rate of CMV reactivation in patients who received letermovir as prophylaxis from day 0 after allogeneic stem cell transplantation (alloSCT) with a control group that did not receive CMV prophylaxis. The primary endpoint was CMV reactivation and was defined as an increase of CMV copies over 1250 Ul/ml in the peripheral blood; secondary endpoints were overall survival (OS) up to 180 days, engraftment and all-cause mortality.
RESULTS RESULTS
We included 21 patients in the control group and 27 patients in the letermovir group. Letermovir treatment led to a significantly reduced incidence of CMV reactivation after alloSCT (33.3% in the letermovir group versus 76.2% in the control group, p<0.001). The OS at day 180 was 80.9% in the control group versus 92.6% in the letermovir group (p<0.05). The median duration of letermovir prophylaxis was 192±104 days.
CONCLUSION CONCLUSIONS
Our results indicate that letermovir prophylaxis is associated with a significant lower risk of CMV reactivation and improved overall survival in CMV-seropositive stem cell recipients. Moreover, a prolonged use of letermovir prophylaxis might be a survival benefit.

Identifiants

pubmed: 36288861
pii: 42/11/5431
doi: 10.21873/anticanres.16047
doi:

Substances chimiques

letermovir 1H09Y5WO1F
Antiviral Agents 0
Acetates 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5431-5441

Informations de copyright

Copyright © 2022 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Katrin Koch (K)

Internal Medicine III, Hematology and Medical Oncology, School of Medicine, Technical University of Munich, Munich, Germany.

Lena Osswald (L)

Internal Medicine III, Hematology and Medical Oncology, School of Medicine, Technical University of Munich, Munich, Germany.

Isabella Miller (I)

Internal Medicine III, Hematology and Medical Oncology, School of Medicine, Technical University of Munich, Munich, Germany.

Krischan Braitsch (K)

Internal Medicine III, Hematology and Medical Oncology, School of Medicine, Technical University of Munich, Munich, Germany.

Katharina Götze (K)

Internal Medicine III, Hematology and Medical Oncology, School of Medicine, Technical University of Munich, Munich, Germany.

Florian Bassermann (F)

Internal Medicine III, Hematology and Medical Oncology, School of Medicine, Technical University of Munich, Munich, Germany.

Peter Herhaus (P)

Internal Medicine III, Hematology and Medical Oncology, School of Medicine, Technical University of Munich, Munich, Germany.

Mareike Verbeek (M)

Internal Medicine III, Hematology and Medical Oncology, School of Medicine, Technical University of Munich, Munich, Germany mareike.verbeek@mri.tum.de.

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Classifications MeSH