Adenovirus infection in hematopoietic stem cell transplantation: Effect of ganciclovir and impact on survival

被引:114
作者
Bruno, B
Gooley, T
Hackman, RC
Davis, C
Corey, L
Boeckh, M
机构
[1] Fred Hutchinson Canc Res Ctr, Program Infect Dis, Div Clin Res, Seattle, WA 98109 USA
[2] Univ Washington, Dept Med, Seattle, WA 98195 USA
[3] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
[4] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[5] Univ Turin, Azienda Osped San Giovanni Battista, Div Ematol, Turin, Italy
关键词
adenovirus; ganciclovir; mortality;
D O I
10.1016/S1083-8791(03)00102-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adenoviruses (ADV) are emerging as important causes of morbidity and mortality in patients undergoing hematopoietic stem cell transplantation (HSCT). In mainly non-T-cell depleted HSCT recipients, we analyzed the incidence of ADV infection, risk factors for infection, the effect of ganciclovir administered for prevention of cytomegalovirus (CMV), and the impact of ADV infection on survival. The overall incidence of ADV, irrespective of the method of detection, was 8.5% (450/5233) and 12.3% (43/348) after the first or second allogeneic HSCT, and 6.3% (78/1219) and 6.5% (5/77) after the first or second autologous HSCT, respectively. The most frequent sites of infection and disease were stool and gastrointestinal tract, respectively. Statistically significant risk factors associated with ADV infections among allogeneic recipients included younger age, grade II to IV graft-versus-host disease, year of transplantation, and a second allogeneic HSCT. Furthermore, allogeneic patients seronegative for CMV at transplantation and seropositive allogeneic patients who did not receive ganciclovir, either at engraftment or as pre-emptive therapy on CMV reactivation, were at higher risk of developing ADV infections compared with seropositive patients who received ganciclovir (odds ratio=1.8, 95% confidence interval (CI) 1.2 to 2.8, P=.005 and odds ratio=3.4, 95% CI 2.1 to 5.55, P<.0001, respectively). The hazard of overall mortality was higher in patients who contracted ADV compared with those who did not (hazard ratio 1.5, 95% CI 1.3 to 1.7, P<.0001). This study shows that ADV infections are associated with poor transplantation outcome in T-cell repleted HSCT recipients. Ganciclovir, given for CMV prevention, may have a protective effect. Controlled treatment and prevention studies are warranted. (C) 2003 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:341 / 352
页数:12
相关论文
共 60 条
[1]   Rapid identification of subgenera of human adenovirus by serological and PCR assays [J].
Akalu, A ;
Seidel, W ;
Liebermann, H ;
Bauer, U ;
Döhner, L .
JOURNAL OF VIROLOGICAL METHODS, 1998, 71 (02) :187-196
[2]   HEMORRHAGIC CYSTITIS ASSOCIATED WITH ADENOVIRUS INFECTION IN BONE-MARROW TRANSPLANTATION [J].
AMBINDER, RF ;
BURNS, W ;
FORMAN, M ;
CHARACHE, P ;
ARTHUR, R ;
BESCHORNER, W ;
SANTOS, G ;
SARAL, R .
ARCHIVES OF INTERNAL MEDICINE, 1986, 146 (07) :1400-1401
[3]   Outcome and clinical course of 100 patients with adenovirus infection following bone marrow transplantation [J].
Baldwin, A ;
Kingman, H ;
Darville, M ;
Foot, ABM ;
Grier, D ;
Cornish, JM ;
Goulden, N ;
Oakhill, A ;
Pamphilon, DH ;
Steward, CG ;
Marks, DI .
BONE MARROW TRANSPLANTATION, 2000, 26 (12) :1333-1338
[4]  
Bertheau P, 1996, BONE MARROW TRANSPL, V17, P295
[5]  
BLANKE C, 1995, AM J MED, V99, P326, DOI 10.1016/S0002-9343(99)80169-7
[6]   Successful modification of a pp65 antigenemia-based early treatment strategy for prevention of cytomegalovirus disease in allogeneic marrow transplant recipients [J].
Boeckh, M ;
Bowden, RA ;
Gooley, T ;
Myerson, D ;
Corey, L .
BLOOD, 1999, 93 (05) :1781-1782
[7]   Cytomegalovirus pp65 antigenemia-guided early treatment with ganciclovir versus ganciclovir at engraftment after allogeneic marrow transplantation: A randomized double-blind study [J].
Boeckh, M ;
Gooley, TA ;
Myerson, D ;
Cunningham, T ;
Schoch, G ;
Bowden, RA .
BLOOD, 1996, 88 (10) :4063-4071
[8]  
Bordigoni Pierre, 2001, Clinical Infectious Diseases, V32, P1290, DOI 10.1086/319984
[9]  
Bruno B, 1996, BLOOD, V88, P1200
[10]  
CASSANO WF, 1991, BONE MARROW TRANSPL, V7, P247