| Literature DB >> 32812351 |
Carlos Solano1,2, Lourdes Vázquez3, Estela Giménez4, Rafael de la Cámara5, Eliseo Albert4, Montserrat Rovira6, Ildefonso Espigado7, Carmen M Calvo8, Javier López-Jiménez9, María Suárez-Lledó6, Anabella Chinea9, Albert Esquirol10, Ariadna Pérez1, Aránzazu Bermúdez11, Raquel Saldaña12, Inmaculada Heras13, Ana J González-Huerta14, Tamara Torrado15, Guiomar Bautista16, Montserrat Batlle17, Santiago Jiménez18, Carlos Vallejo19, Pere Barba20, María Á Cuesta21, José L Piñana22,23, David Navarro4,24.
Abstract
The net impact of cytomegalovirus (CMV) DNAemia on overall mortality (OM) and nonrelapse mortality (NRM) following allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains a matter of debate. This was a retrospective, multicenter, noninterventional study finally including 749 patients. CMV DNA monitoring was conducted by real-time polymerase chain reaction (PCR) assays. Clinical outcomes of interest were OM and NRM through day 365 after allo-HSCT. The cumulative incidence of CMV DNAemia in this cohort was 52.6%. A total of 306 out of 382 patients with CMV DNAemia received preemptive antiviral therapy (PET). PET use for CMV DNAemia, but not the occurrence of CMV DNAemia, taken as a qualitative variable, was associated with increased OM and NRM in univariate but not in adjusted models. A subcohort analysis including patients monitored by the COBAS Ampliprep/COBAS Taqman CMV Test showed that OM and NRM were comparable in patients in whom either low or high plasma CMV DNA threshold (<500 vs ≥500 IU/mL) was used for PET initiation. In conclusion, CMV DNAemia was not associated with increased OM and NRM in allo-HSCT recipients. The potential impact of PET use on mortality was not proven but merits further research.Entities:
Keywords: bone marrow/hematopoietic stem cell transplantation; clinical research/practice; complication: infectious; infection and infectious agents - viral: Cytomegalovirus (CMV)
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Year: 2020 PMID: 32812351 DOI: 10.1111/ajt.16147
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086