CMV reactivation during pretransplantation evaluation: a novel risk factor for posttransplantation CMV reactivation.

Détails

ID Serval
serval:BIB_E4F083BC2BE9
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
CMV reactivation during pretransplantation evaluation: a novel risk factor for posttransplantation CMV reactivation.
Périodique
Blood advances
Auteur⸱e⸱s
Zamora D., Xie H., Sadowska-Klasa A., Kampouri E., Biernacki M.A., Ueda Oshima M., Duke E., Green M.L., Kimball L.E., Holmberg L., Waghmare A., Greninger A.L., Jerome K.R., Hill G.R., Hill J.A., Leisenring W.M., Boeckh M.J.
ISSN
2473-9537 (Electronic)
ISSN-L
2473-9529
Statut éditorial
Publié
Date de publication
10/09/2024
Peer-reviewed
Oui
Volume
8
Numéro
17
Pages
4568-4580
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
Publication Status: ppublish
Résumé
Cytomegalovirus (CMV) disease occurs occasionally before allogeneic hematopoietic cell transplantation (HCT) and is associated with poor post-HCT outcomes; however, the impact of pre-HCT CMV reactivation is unknown. Pre-HCT CMV reactivation was assessed in HCT candidates from the preemptive antiviral therapy (2007-2017) and letermovir prophylaxis (2018-2021) eras. CMV DNA polymerase chain reaction (PCR) surveillance was routinely performed during the pre-HCT workup period, and antiviral therapy was recommended according to risk of progression to CMV disease. Risk factors for pre-HCT CMV reactivation were characterized, and the associations of pre-HCT CMV reactivation with post-HCT outcomes were examined using logistic regression and Cox proportional hazard models, respectively. A total of 1694 patients were identified, and 11% had pre-HCT CMV reactivation 14 days (median; interquartile range [IQR], 6-23) before HCT. Lymphopenia (≤0.3 × 103/μL) was the strongest risk factor for pre-HCT CMV reactivation at multiple PCR levels. In the preemptive therapy era, patients with pre-HCT CMV reactivation had a significantly increased risk of CMV reactivation by day 100 as well as CMV disease and death by 1 year after HCT. Clearance of pre-HCT CMV reactivation was associated with a lower risk of post-HCT CMV reactivation. Similar associations with post-HCT CMV end points were observed in a cohort of patients receiving letermovir prophylaxis. Pre-HCT CMV reactivation can be routinely detected in high-risk HCT candidates and is a significant risk factor for post-HCT CMV reactivation and disease. Pre-HCT CMV DNA PCR surveillance is recommended in high-risk HCT candidates, and antiviral therapy may be indicated to prevent post-HCT CMV reactivation.
Mots-clé
Humans, Cytomegalovirus Infections/etiology, Hematopoietic Stem Cell Transplantation/adverse effects, Virus Activation, Risk Factors, Male, Cytomegalovirus/physiology, Middle Aged, Female, Adult, Antiviral Agents/therapeutic use, Aged
Pubmed
Web of science
Open Access
Oui
Création de la notice
10/01/2025 12:23
Dernière modification de la notice
13/01/2025 8:04
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