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更昔洛韦预防异基因骨髓移植受者的巨细胞病毒感染和疾病。一项安慰剂对照、双盲试验的结果。

Ganciclovir prophylaxis of cytomegalovirus infection and disease in allogeneic bone marrow transplant recipients. Results of a placebo-controlled, double-blind trial.

作者信息

Winston D J, Ho W G, Bartoni K, Du Mond C, Ebeling D F, Buhles W C, Champlin R E

机构信息

UCLA Center for the Health Sciences.

出版信息

Ann Intern Med. 1993 Feb 1;118(3):179-84. doi: 10.7326/0003-4819-118-3-199302010-00004.

Abstract

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-sero-positive bone marrow transplant recipients but is frequently associated with neutropenia.

摘要

目的

评估更昔洛韦预防巨细胞病毒(CMV)感染及疾病的疗效和安全性。

设计

一项随机、安慰剂对照、双盲试验。

地点

大学附属骨髓移植中心。

患者

CMV血清学阳性的异基因骨髓移植受者。

干预措施

随机分组,在移植前1周接受安慰剂或每8小时2.5mg/kg体重的更昔洛韦治疗,共1周,移植后当移植后中性粒细胞计数达到1.0×10⁹/L时,周一至周五每天接受6mg/kg的更昔洛韦治疗。

测量指标

巨细胞病毒感染(培养阳性、血清学转换、组织学检查阳性)、CMV疾病(肺炎、胃肠炎、消瘦综合征)以及研究药物毒性。

结果

45名接受安慰剂治疗的患者中有25名(56%)发生CMV感染,而40名接受更昔洛韦治疗的患者中仅有8名(20%)发生(P<0.001)。更昔洛韦治疗组患者发生CMV疾病的情况可能也较少(40名患者中有4名[10%],而45名患者中有11名[24%];P=0.09)。移植后120天内发生CMV疾病的概率在安慰剂组患者中为0.29,而在更昔洛韦组患者中仅为0.12(P=0.06)。可逆性中性粒细胞减少是与更昔洛韦相关的唯一明显毒性反应,43名接受更昔洛韦治疗的患者中有25名(58%)以及47名接受安慰剂治疗的患者中有13名(28%)在移植后需要中断研究药物治疗(P=0.005)。安慰剂组患者(45名中的29名[64%])和更昔洛韦组患者(40名中的28名[70%])的总体生存率相似(P>0.2)。

结论

移植前开始并在移植后中性粒细胞计数恢复后继续使用的预防性更昔洛韦,可降低CMV血清学阳性骨髓移植受者CMV感染的发生率和严重程度,但常与中性粒细胞减少相关。

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