High-risk adenovirus-infected pediatric allogeneic hematopoietic progenitor cell transplant recipients and preemptive cidofovir therapy

被引:60
作者
Anderson, Evan J. [1 ,2 ]
Guzman-Cottrill, Judith A. [1 ]
Kletzel, Morris [3 ]
Thormann, Kimberly [3 ]
Sullivan, Christine [4 ]
Zheng, Xiaotian [5 ]
Katz, Ben Z. [1 ]
机构
[1] Northwestern Univ, Div Pediat Infect Dis, Dept Pediat, Feinberg Sch Med,Childrens Mem Hosp, Chicago, IL 60614 USA
[2] Northwestern Univ, Div Infect Dis, Dept Med, Feinberg Sch Med,NW Mem Hosp, Chicago, IL 60614 USA
[3] Northwestern Univ, Div Hematol Oncol & Stem Cell Transplantat, Dept Pediat, Feinberg Sch Med,Childrens Mem Hosp, Chicago, IL 60614 USA
[4] Childrens Mem Hosp, Mary Ann & J Milburn Smith Child Hlth Res Core Pr, Chicago, IL 60614 USA
[5] Northwestern Univ, Dept Pathol, Feinberg Sch Med, Childrens Mem Hosp, Chicago, IL 60614 USA
关键词
hematopoietic progenitor cell transplantation; adenovirus; infection; cidofovir treatment;
D O I
10.1111/j.1399-3046.2007.00851.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
ADV has emerged as an important pathogen in children undergoing allogeneic HPCT. A prospective study of the epidemiology of ADV infection and preemptive therapy of high risk ADV infections in children undergoing HPCT was undertaken. Cultures of throat, urine, and stool for viral pathogens and plasma for ADV PCR were obtained prior to transplantation, weekly for the first 100 days, and then monthly for one yr. Children developing high-risk ADV infections were treated preemptively with cidofovir 1 mg/kg/day given three times weekly for three wk. A case-controlled study was performed to identify risk factors for high-risk ADV infections. Seven (18%) of the 38 subjects developed high-risk ADV infections usually within 100 days of HPCT and were preemptively treated with i.v. cidofovir at a dose of 1 mg/kg/dose three times weekly for nine doses. High-risk ADV infections resolved in all seven patients without renal toxicity. CMV viremia occurred in two of seven patients during or shortly after therapy with cidofovir. A case-control study did not identify any risk factors that achieved statistical significance. Treatment with a modified dosing regimen of cidofovir was well-tolerated and high-risk ADV infections resolved in all patients.
引用
收藏
页码:219 / 227
页数:9
相关论文
共 35 条
[1]   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
[2]  
BLANKE C, 1995, AM J MED, V99, P326, DOI 10.1016/S0002-9343(99)80169-7
[3]  
Bordigoni Pierre, 2001, Clinical Infectious Diseases, V32, P1290, DOI 10.1086/319984
[4]   Adenovirus infection in hematopoietic stem cell transplantation: Effect of ganciclovir and impact on survival [J].
Bruno, B ;
Gooley, T ;
Hackman, RC ;
Davis, C ;
Corey, L ;
Boeckh, M .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2003, 9 (05) :341-352
[5]   Adenovirus infections in stem cell transplant recipients: Recent developments in understanding of pathogenesis, diagnosis and management [J].
Chakrabarti, S ;
Milligan, DW ;
Moss, PAH ;
Mautner, V .
LEUKEMIA & LYMPHOMA, 2004, 45 (05) :873-885
[6]   Adenovirus infections following allogeneic stem cell transplantation: incidence and outcome in relation to graft manipulation, immunosuppression, and immune recovery [J].
Chakrabarti, S ;
Mautner, V ;
Osman, H ;
Collingham, KE ;
Fegan, CD ;
Klapper, PE ;
Moss, PAH ;
Milligan, DW .
BLOOD, 2002, 100 (05) :1619-1627
[7]   Evaluation of Cidofovir (HPMPC, GS-504) against adenovirus type 5 infection in vitro and in a New Zealand rabbit ocular model [J].
deOliveira, CBR ;
Stevenson, D ;
LaBree, L ;
McDonnell, PJ ;
Trousdale, MD .
ANTIVIRAL RESEARCH, 1996, 31 (03) :165-172
[8]   Prediction of severe disseminated adenovirus infection by serum PCR [J].
Echavarria, M ;
Forman, M ;
van Tol, MJD ;
Vossen, JM ;
Charache, P ;
Kroes, ACM .
LANCET, 2001, 358 (9279) :384-385
[9]   INCREASING INCIDENCE OF ADENOVIRUS DISEASE IN BONE-MARROW TRANSPLANT RECIPIENTS [J].
FLOMENBERG, P ;
BABBITT, J ;
DROBYSKI, WR ;
ASH, RC ;
CARRIGAN, DR ;
SEDMAK, GV ;
MCAULIFFE, T ;
CAMITTA, B ;
HOROWITZ, MH ;
BUNIN, N ;
CASPER, JT .
JOURNAL OF INFECTIOUS DISEASES, 1994, 169 (04) :775-781
[10]   Intravenous ribavirin treatment for severe adenovirus disease in immunocompromised children [J].
Gavin, PJ ;
Katz, BZ .
PEDIATRICS, 2002, 110 (01) :e9