Cytomegalovirus Infection in Patients Who Underwent Allogeneic Hematopoietic Stem Cell Transplantation in Portugal: A Five-Year Retrospective Review

被引:46
作者
Sousa, Hugo [1 ,2 ,3 ]
Boutolleau, David [4 ,5 ,6 ]
Ribeiro, Joana [1 ,2 ,3 ]
Teixeira, Ana L. [1 ,2 ]
Vaz, Carlos Pinho [7 ]
Campilho, Fernando [7 ]
Branca, Rosa [7 ]
Campos, Antonio, Jr. [7 ]
Baldaque, Ines [1 ]
Medeiros, Rui [1 ,2 ,8 ]
机构
[1] Portuguese Inst Oncol Porto, Virol Serv, Oporto, Portugal
[2] Portuguese Inst Oncol Porto, Mol Oncol Grp, Oporto, Portugal
[3] Univ Porto, Fac Med, P-4100 Oporto, Portugal
[4] Univ Paris 06, Sorbonne Univ, CR7, Ctr Immunol & Malad Infect CIMI Paris, Paris, France
[5] CIMI Paris, INSERM, U1135, Paris, France
[6] Hop Univ Pitie Salpetriere Charles Foix, AP HP, Serv Virol, Paris, France
[7] Portuguese Inst Oncol Porto, Bone Marrow Transplantat Unit, Oporto, Portugal
[8] Portuguese League Canc LPCC NRNorte, Res Dept, Oporto, Portugal
关键词
Hematopoietic stem cell transplantation; Graft-versus-host disease; Mortality; Cytomegalovirus; BONE-MARROW-TRANSPLANTATION; CORD BLOOD TRANSPLANTATION; MATCHED SIBLING DONOR; REAL-TIME PCR; RISK-FACTORS; VIRAL LOAD; SOLID-ORGAN; PREEMPTIVE TREATMENT; LEUKEMIA PATIENTS; CMV ANTIGENEMIA;
D O I
10.1016/j.bbmt.2014.08.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cytomegalovirus (CMV) infection is 1 of the leading causes of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (aHSCT), mainly within the first 100 days after transplantation. We aimed to characterize CMV infection in a cohort of 305 patients with different malignancies undergoing aHSCT at the Portuguese Institute of Oncology of Porta between January 2008 and December 2012. In total, 184 patients (60.3%) developed CMV infection, mainly viral reactivations rather than primary infections (96.2% versus 3.8%, respectively). The majority of patients (166 of 184) developed CMV infection <= 100 days after transplantation, with median time to infection of 29 days (range, 0 to 1285) and median duration of infection of 10 days (range, 2 to 372). Multivariate analysis revealed that CMV infection was increased in donor (D)-/recipient (R)+ and D+/R+ (odds ratio [OR], 10.5; 95% confidence interval [CI], 4.35 to 25.4; P < .001) and in patients with mismatched or unrelated donors (OR, 2.54; 95% Cl, 1.34 to 4.80; P = .004). Cox regression model showed that the risk of death was significantly increased in patients >38 years old (OR, 1.89; 95% CI, 1.14 to 3.12; P = .0137), who underwent transplantation with peripheral blood (OR, 3.02; 95% CI, 1.33 to 6.86; P = .008), with mismatched or unrelated donor (OR, 2.16; 95% Cl, 1.48 to 3.13; P < .001), and who developed CMV infection (OR, 1.76; 95% CI, 1.07 to 2.90; P = .025). Moreover, patients who developed CMV infection had a significantly reduced median post-transplantation survival (16 versus 36 months; P = .002). (C) 2014 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:1958 / 1967
页数:10
相关论文
共 61 条
[1]   ALLOGENEIC MARROW TRANSPLANTATION FOR CHRONIC MYELOID-LEUKEMIA [J].
APPLEBAUM, FR ;
CLIFT, R ;
BUCKNER, CD ;
ANASETTI, C ;
RADICH, J ;
HIGANO, T ;
STORB, R ;
HANSEN, J ;
THOMAS, ED .
MEDICAL ONCOLOGY, 1994, 11 (02) :69-74
[2]   Improving Safety of Preemptive Therapy with Oral Valganciclovir for Cytomegalovirus Infection after Allogeneic Hematopoietic Stem Cell Transplantation [J].
Barkam, Corinna ;
Kamal, Haytham ;
Dammann, Elke ;
Diedrich, Helmut ;
Buchholz, Stefanie ;
Eder, Matthias ;
Krauter, Juergen ;
Ganser, Arnold ;
Stadler, Michael .
BONE MARROW RESEARCH, 2012,
[3]   Relapse after allogeneic stem cell transplantation [J].
Barrett, A. John ;
Battiwalla, Minoo .
EXPERT REVIEW OF HEMATOLOGY, 2010, 3 (04) :429-441
[4]   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
[5]   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
[6]  
Boeckh M, 1999, ADV EXP MED BIOL, V458, P89
[7]  
Boeckh M, 1999, Transpl Infect Dis, V1, P165, DOI 10.1034/j.1399-3062.1999.010305.x
[8]   How I treat cytomegalovirus in hematopoietic cell transplant recipients [J].
Boeckh, Michael ;
Ljungman, Per .
BLOOD, 2009, 113 (23) :5711-5719
[9]   Survey of CMV management in pediatric allogeneic HSCT programs, on behalf of the Inborn Errors, Infectious Diseases and Pediatric Diseases Working Parties of EBMT [J].
Bontant, T. ;
Sedlacke, P. ;
Balduzzi, A. ;
Gaspar, B. ;
Cesaro, S. ;
Einsele, H. ;
Peters, C. ;
Dalle, J-H .
BONE MARROW TRANSPLANTATION, 2014, 49 (02) :276-279
[10]   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