GANCICLOVIR PROPHYLAXIS OF CYTOMEGALOVIRUS-INFECTION AND DISEASE IN ALLOGENEIC BONE-MARROW TRANSPLANT RECIPIENTS - RESULTS OF A PLACEBO-CONTROLLED, DOUBLE-BLIND TRIAL

被引:351
作者
WINSTON, DJ [1 ]
HO, WG [1 ]
BARTONI, K [1 ]
DUMOND, C [1 ]
EBELING, DF [1 ]
BUHLES, WC [1 ]
CHAMPLIN, RE [1 ]
机构
[1] SYNTEX INC, INST CLIN MED, PALO ALTO, CA 94304 USA
关键词
BONE MARROW TRANSPLANTATION; CYTOMEGALOVIRUSES; CYTOMEGALIC INCLUSION DISEASE; TRANSPLANTATION; HOMOLOGOUS; GANCICLOVIR;
D O I
10.7326/0003-4819-118-3-199302010-00004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate the efficacy and safety of ganciclovir for prevention of cytomegalovirus (CMV) infection and disease. Design: A randomized, placebo-controlled, double-blind trial. Setting: University-affiliated bone marrow transplant center. Patients: Cytomegalovirus-seropositive allogeneic bone marrow transplant recipients. Interventions: Random assignment to receive either a placebo or ganciclovir at a dose of 2.5 mg/kg body weight every 8 hours for 1 week before transplant and then at a dose of 6 mg/kg once per day, Monday through Friday, after transplant when the post-transplant neutrophil count reached 1.0 x 10(9)/L. Measurements: Cytomegalovirus infection (positive culture, seroconversion, positive histologic findings), CMV disease (pneumonia, gastroenteritis, the wasting syndrome), and study-drug toxicity. Results: Cytomegalovirus infection developed in 25 of 45 placebo patients (56%) but in only 8 of 40 ganciclovir patients (20%) (P < 0.001). Cytomegalovirus disease may also have occurred less often in the ganciclovir patients (4 of 40 patients [10%] versus 11 of 45 patients [24%]; P = 0.09). The probability of CMV disease occurring within the first 120 days after transplantation was 0.29 among the placebo patients but only 0.12 among ganciclovir patients (P = 0.06). Reversible neutropenia was the only appreciable toxicity related to ganciclovir and required interruption of the study drug after transplant in 25 of 43 ganciclovir patients (58%) and in 13 of 47 placebo patients (28%) (P = 0.005). Overall survival was similar in both the placebo patients (29 of 45 [64%]) and ganciclovir patients (28 of 40 [70%]; P > 0.2). Conclusions: Prophylactic ganciclovir, started before transplant and continued after recovery of the post-transplant neutrophil count, reduces the incidence and severity of CMV infection in CMV-seropositive bone marrow transplant recipients but is frequently associated with neutropenia.
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页码:179 / 184
页数:6
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