Rising pp65 antigenemia during preemptive anticytomegalovinus therapy after allogeneic hematopoietic stem cell transplantation: risk factors, correlation with DNA load, and outcomes

被引:161
作者
Nichols, WG
Corey, L
Gooley, T
Drew, WL
Miner, R
Huang, ML
Davis, C
Boeckh, M
机构
[1] Fred Hutchinson Canc Res Ctr, Program Infect Dis, Seattle, WA 98109 USA
[2] Univ Washington, Seattle, WA 98195 USA
[3] Univ Calif San Francisco, Dept Lab Med, Med Ctr, San Francisco, CA 94143 USA
关键词
D O I
10.1182/blood.V97.4.867
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To determine the risk factors and outcomes associated with rising cytomegalovirus (CMV) antigenemia levels during preemptive therapy among stem cell allograft recipients, 119 patients with CMV antigenemia were studied. Patients were prospectively monitored for CMV antigenemia weekly; those with positive findings on antigenemia tests were treated with intravenous ganciclovir (5 mg/kg twice daily for 1 week, followed by 5 mg/kg per day for 5-6 d/wk). While on therapy, 47 of 119 (39%) patients demonstrated increases that were 2 or more times greater than their baseline values, whereas 33 of 119 (28%) patients demonstrated increases that were 5 or more times greater. Rising antigenemia was confirmed by polymerase chain reaction for CMV DNA. Multivariate analysis identified corticosteroids as the primary risk factor for increasing antigenemia: for increases greater than or equal to twice the baseline, 1 to 2 mg/kg steroids was associated with an odds ratio (OR) of 4.0. For increases greater than or equal to 2 mglkg steroids, the OR was 10.1. CMV isolates obtained at the time of rising antigenemia were susceptible to ganciclovir, indicating that resistance was not a major factor. Overall, rising antigenemia levels were not correlated with CMV disease. All 4 patients in whom CMV disease developed during therapy, however, had rising antigenemia levels. Among the 47 patients with antigenemia increases greater than or equal to twice the baseline, 15 were re-induced with antivirals, whereas 32 continued to receive maintenance therapy. All 4 patients in whom CMV disease developed during therapy received maintenance therapy, and 3 died with CMV disease. Thus, host factors such as the receipt of corticosteroids explain increasing viral load during the early phase of preemptive therapy. Continued induction dosing or re-induction may protect against early breakthrough CMV disease and CMV-related death among patients with rising antigenemia on preemptive therapy. (C) 2001 by The American Society of Hematology.
引用
收藏
页码:867 / 874
页数:8
相关论文
共 27 条
[21]  
LYNCH MHE, 1995, BONE MARROW TRANSPL, V15, P59
[22]  
PRZEPIORKA D, 1994, BONE MARROW TRANSPL, V13, P461
[23]  
PRZEPIORKA D, 1995, BONE MARROW TRANSPL, V15, P825
[24]   Development of a high-throughput quantitative assay for detecting herpes simplex virus DNA in clinical samples [J].
Ryncarz, AJ ;
Goddard, J ;
Wald, A ;
Huang, ML ;
Roizman, B ;
Corey, L .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (06) :1941-1947
[25]  
Salzberger B, 1997, BLOOD, V90, P2502
[26]   A comparison of prophylactic vs pre-emptive ganciclovir to prevent cytomegalovirus disease after T-depleted volunteer unrelated donor bone marrow transplantation [J].
Stocchi, R ;
Szydlo, R ;
Craddock, C ;
Kanfer, E ;
Apperley, JF ;
Goldman, JM ;
Ward, KN .
BONE MARROW TRANSPLANTATION, 1999, 23 (07) :705-709
[27]  
STORB R, 1994, BLOOD, V83, P2749