Impact of Cytomegalovirus (CMV) Reactivation after Umbilical Cord Blood Transplantation

被引:85
作者
Beck, Jill C. [1 ]
Wagner, John E. [1 ]
DeFor, Todd E. [1 ]
Brunstein, Claudio G. [2 ]
Schleiss, Mark R. [1 ]
Young, Jo-Anne [2 ]
Weisdorf, Daniel H. [2 ]
Cooley, Sarah [2 ]
Miller, Jeffrey S. [2 ]
Verneris, Michael R. [1 ]
机构
[1] Univ Minnesota, Dept Pediat, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Div Blood & Marrow Transplantat, Dept Med, Minneapolis, MN 55455 USA
关键词
Cytomegalovirus; Cord blood transplantation; Prophylaxis; GVHD; STEM-CELL TRANSPLANTATION; BONE-MARROW-TRANSPLANTATION; VERSUS-HOST-DISEASE; SINGLE-INSTITUTE EXPERIENCE; PREDICTS SUPERIOR SURVIVAL; LYMPHOCYTE RECOVERY; RISK-FACTORS; PERIPHERAL-BLOOD; INFECTION; DONOR;
D O I
10.1016/j.bbmt.2009.09.019
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
This study investigated the impact of pretransplant cytomegalovirus (CMV) serostatus and posttransplant CMV reactivation and disease on umbilical cord blood transplant (UCBT) outcomes. Between 1994 and 2007, 332 patients with hematologic malignancies underwent UCBT and 54% were CMV seropositive. Pre-transplant recipient CMV serostatus had no impact on acute or chronic graft-versus-host disease (aGVHD, cGVHD), relapse, disease-free survival (DFS), or overall survival (OS). There was a trend toward greater day 100 treatment-related mortality (TRM) in CMV-seropositive recipients (P=.07). CMV reactivation occurred in 51% (92/180) of patients with no difference in myeloablative (MA) versus reduced-intensity conditioning (RIC) recipients (P=.33). Similarly, reactivation was not influenced by the number of UCB units transplanted, the degree of HLA disparity, the CD34(+) or CD3(+) cell dose, or donor killer cell immunoglobulin-like receptor (KIR) gene haplotype. Rapid lymphocyte recovery was associated with CMV reactivation (P=.02). CMV reactivation was not associated with aGVHD (P=.97) or cGVHD (P=.65), nor did it impact TRM (P=.88), relapse (P=.62), or survival (P=.78). CMV disease occurred in 13.8% of the CMV-seropositive patients, resulting in higher TRM (P=.01) and lower OS (P=.02). Thus, although recipient CMV serostatus and CMV reactivation have little demonstrable impact on UCB transplant outcomes, the development of CMV disease remains a risk, associated with inferior outcomes. Biol Blood Marrow Transplant 16: 215-222 (2010) (C) 2010 American Society for Blood and Marrow Transplantation
引用
收藏
页码:215 / 222
页数:8
相关论文
共 52 条
[1]
Umbilical cord blood transplantation and cytomegalovirus: posttransplantation infection and donor screening [J].
Albano, Maria S. ;
Taylor, Patricia ;
Pass, Robert F. ;
Scaradavou, Andromachi ;
Ciubotariu, Rodica ;
Carrier, Carmelita ;
Dobrila, Ludy ;
Rubinstein, Pablo ;
Stevens, Cladd E. .
BLOOD, 2006, 108 (13) :4275-4282
[2]
Prolonged survival in adults with acute lymphoblastic leukemia after reduced-intensity conditioning with cord blood or sibling donor transplantation [J].
Bachanova, Veronika ;
Verneris, Michael R. ;
DeFor, Todd ;
Brunstein, Claudio G. ;
Weisdorf, Daniel J. .
BLOOD, 2009, 113 (13) :2902-2905
[3]
Serious infections after unrelated donor transplantation in 136 children: Impact of stem cell source [J].
Barker, JN ;
Hough, RE ;
van Burik, JAH ;
DeFor, TE ;
MacMillan, ML ;
O'Brien, MR ;
Wagner, JE .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2005, 11 (05) :362-370
[4]
Umbilical-cord blood transplantation for the treatment of cancer [J].
Barker, JN ;
Wagner, JE .
NATURE REVIEWS CANCER, 2003, 3 (07) :526-532
[5]
Donor and Recipient CMV Serostatus and Outcome of Pediatric Allogeneic HSCT for Acute Leukemia in the Era of CMV-Preemptive Therapy [J].
Behrendt, Carolyn E. ;
Rosenthal, Joseph ;
Bolotin, Ellen ;
Nakamura, Ryotaro ;
Zaia, John ;
Forman, Stephen J. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2009, 15 (01) :54-60
[6]
Cytomegalovirus in hematopoietic stem cell transplant recipients: Current status, known challenges, and future strategies [J].
Boeckh, M ;
Nichols, WG ;
Papanicolaou, G ;
Rubin, R ;
Wingard, JR ;
Zaia, Y .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2003, 9 (09) :543-558
[7]
Late cytomegalovirus disease and mortality in recipients of allogeneic hematopoietic stem cell transplants: importance of viral load and T-cell immunity [J].
Boeckh, M ;
Leisenring, W ;
Riddell, SR ;
Bowden, RA ;
Huang, ML ;
Myerson, D ;
Stevens-Ayers, T ;
Flowers, MED ;
Cunningham, T ;
Corey, L .
BLOOD, 2003, 101 (02) :407-414
[8]
Surveillance of cytomegalovirus (CMV) DNAemia in pediatric allogeneic stem cell transplantation: incidence and outcome of CMV infection and disease [J].
Bordon, V. ;
Bravo, S. ;
Van Renterghem, L. ;
de Moerloose, B. ;
Benoit, Y. ;
Laureys, G. ;
Dhooge, C. .
TRANSPLANT INFECTIOUS DISEASE, 2008, 10 (01) :19-23
[9]
Increased transplant-related morbidity and mortality in CMV-seropositive patients despite highly effective prevention of CMV disease after allogeneic T-cell-depleted stem cell transplantation [J].
Broers, AEC ;
van der Holt, R ;
van Esser, JWJ ;
Gratama, JW ;
Henzen-Logmans, S ;
Kuenen-Boumeester, V ;
Löwenberg, B ;
Cornelissen, JJ .
BLOOD, 2000, 95 (07) :2240-2245
[10]
Randomized clinical trial of ganciclovir vs acyclovir for prevention of cytomegalovirus antigenemia after allogeneic transplantation [J].
Burns, LJ ;
Miller, W ;
Kandaswamy, C ;
DeFor, TE ;
MacMillan, ML ;
van Burik, JA ;
Weisdorf, DJ .
BONE MARROW TRANSPLANTATION, 2002, 30 (12) :945-951