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Clinical outcomes of allogeneic hematopoietic stem cell transplant recipients developing Cytomegalovirus DNAemia prior to engraftment

Authors :
Rafael de la Cámara
Raquel Saldaña
María Ángeles Cuesta
Aránzazu Bermúdez
Ana Julia Gonzalez-Huerta
Anabella Chinea
David Navarro
José Luis Piñana
Carlos Solano
Montserrat Batlle
Carmen Martín Calvo
Tamara Torrado
Estela Giménez
Lourdes Vázquez
Inmaculada Heras
Pere Barba
Montserrat Rovira
Javier López-Jiménez
Eliseo Albert
Ariadna Pérez
Albert Esquirol
Ildefonso Espigado
María Suárez-Lledó
Santiago Leguey Jiménez
Carlos Vallejo
Source :
Bone Marrow Transplantation, r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol, instname, BONE MARROW TRANSPLANTATION, r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Publication Year :
2020

Abstract

There is limited information on the impact of CMV DNAemia episodes developing prior to engraftment (pre-CMV DNAemia) on clinical outcomes following allogeneic hematopoietic stem cell transplantation (allo-HSCT). This issue was addressed in the current retrospective multicenter study including 878 patients. All participant centers used preemptive antiviral therapy strategies for prevention of CMV disease. CMV DNA load in blood was monitored by real-time PCR assays. A total of 144 patients (cumulative incidence 16.5%, 95% CI, 14%-19%) had an episode of pre-CMV DNAemia at a median of 10 days after allo-HSCT. Patients who developed pre-CMV DNAemia had a significantly higher (P = < 0.001) probability of recurrent episodes (50%) than those who experienced post-CMV DNAemia (32.9%); Nevertheless, the incidence of CMV disease was comparable (P = 0.52). Cumulative incidences of overall mortality (OM) and non-relapse mortality (NRM) at 1-year after allo-HSCT were 32% (95% CI, 29-35%) and 23% (95% CI 20-26%), respectively. The risk of OM and NRM in adjusted models appeared comparable in patients developing a single episode of CMV DNAemia, regardless of whether it occurred before or after engraftment, in patients with pre- and post-engraftment CMV DNAemia episodes or in those without CMV DNAemia.

Details

ISSN :
14765365 and 02683369
Volume :
56
Issue :
6
Database :
OpenAIRE
Journal :
Bone marrow transplantation
Accession number :
edsair.doi.dedup.....7f9231a827865fd4f2b30fc2bcd7b584