Impact of Cytomegalovirus Reactivation and Natural Killer Reconstitution on Outcomes after Allogeneic Hematopoietic Stem Cell Transplantation: A Single-Center Analysis.
Adolescent
Adult
Aged
Allografts
Cytomegalovirus
/ physiology
Cytomegalovirus Infections
/ blood
Disease-Free Survival
Female
Follow-Up Studies
Hematologic Neoplasms
/ mortality
Hematopoietic Stem Cell Transplantation
Humans
Killer Cells, Natural
/ metabolism
Male
Middle Aged
Survival Rate
Virus Activation
Allogeneic stem cell transplantation
Cytomegalovirus reactivation
Natural killer cell reconstitution
Nonrelapse mortality
Journal
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
ISSN: 1523-6536
Titre abrégé: Biol Blood Marrow Transplant
Pays: United States
ID NLM: 9600628
Informations de publication
Date de publication:
01 2020
01 2020
Historique:
received:
05
07
2019
revised:
17
09
2019
accepted:
24
09
2019
pubmed:
30
9
2019
medline:
22
1
2021
entrez:
30
9
2019
Statut:
ppublish
Résumé
Cytomegalovirus (CMV) reactivation and natural killer (NK) cell reconstitution are well-recognized immunologic events occurring after allogeneic stem cell transplantation (allo-SCT). We aimed to study the outcome of CMV reactivation (CMVR) and NK cell reconstitution in patients with hematologic malignancies after allo-SCT. We retrospectively studied 246 adult patients (152 men, 94 women; median age, 51 years [range, 18 to 69]) who underwent allo-SCT for hematologic malignancies at the Kanagawa Cancer Center. CMVR was defined as initiation of preemptive CMV therapy after pp65 antigenemia surveillance. All patients' lymphocyte subsets were monitored by flow cytometry at 180, 365, and 730 days post-transplant. The median follow-up period was 3.2 years (range, .8 to 9.6 years). CMVR occurred in 141 patients (57%) at a median of 45 days (range, 15 to 93). In patients without CMVR (CMVR-) versus those with CMVR (CMVR+), 5-year overall survival (OS), nonrelapse mortality (NRM), and cumulative incidence of relapse (CIR) were 79% versus 55% (P < .001), 3% versus 16% (P = .012), and 28% versus 38% (P = .09), respectively. CD8
Identifiants
pubmed: 31563574
pii: S1083-8791(19)30639-1
doi: 10.1016/j.bbmt.2019.09.028
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
171-177Informations de copyright
Copyright © 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.