Combination Antifungal Therapy for Cryptococcal Meningitis

被引:0
|
作者
Day, Jeremy N. [1 ,3 ]
Chau, Tran T. H. [1 ,2 ]
Wolbers, Marcel [1 ,3 ]
Mai, Pham P. [2 ]
Dung, Nguyen T. [2 ]
Mai, Nguyen H. [1 ,2 ]
Phu, Nguyen H. [1 ,2 ]
Nghia, Ho D. [1 ,2 ]
Phong, Nguyen D. [2 ]
Thai, Cao Q. [1 ]
Thai, Le H. [1 ]
Chuong, Ly V. [2 ]
Sinh, Dinh X. [2 ]
Duong, Van A. [1 ]
Hoang, Thu N. [1 ]
Diep, Pham T. [1 ]
Campbell, James I. [3 ]
Sieu, Tran P. M. [2 ]
Baker, Stephen G. [1 ,3 ]
Chau, Nguyen V. V. [2 ]
Hien, Tran T. [1 ,3 ]
Lalloo, David G. [4 ]
Farrar, Jeremy J. [1 ,3 ]
机构
[1] Univ Oxford, Clin Res Unit, Wellcome Trust Major Overseas Programme Vietnam, Ho Chi Minh City, Vietnam
[2] Hosp Trop Dis, Ho Chi Minh City, Vietnam
[3] Univ Oxford, Ctr Trop Med, Liverpool, Merseyside, England
[4] Univ Oxford, Liverpool Sch Trop Med, Liverpool, Merseyside, England
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2013年 / 368卷 / 14期
基金
英国惠康基金;
关键词
ACQUIRED-IMMUNODEFICIENCY-SYNDROME; HIGH-DOSE FLUCONAZOLE; AMPHOTERICIN-B; RANDOMIZED-TRIAL; AIDS; FLUCYTOSINE; MULTIPLICITY; GUIDELINES; MANAGEMENT;
D O I
10.1056/NEJMoa1110404
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Combination antifungal therapy (amphotericin B deoxycholate and flucytosine) is the recommended treatment for cryptococcal meningitis but has not been shown to reduce mortality, as compared with amphotericin B alone. We performed a randomized, controlled trial to determine whether combining flucytosine or high-dose fluconazole with high-dose amphotericin B improved survival at 14 and 70 days. METHODS We conducted a randomized, three-group, open-label trial of induction therapy for cryptococcal meningitis in patients with human immunodeficiency virus infection. All patients received amphotericin B at a dose of 1 mg per kilogram of body weight per day; patients in group 1 were treated for 4 weeks, and those in groups 2 and 3 for 2 weeks. Patients in group 2 concurrently received flucytosine at a dose of 100 mg per kilogram per day for 2 weeks, and those in group 3 concurrently received fluconazole at a dose of 400 mg twice daily for 2 weeks. RESULTS A total of 299 patients were enrolled. Fewer deaths occurred by days 14 and 70 among patients receiving amphotericin B and flucytosine than among those receiving amphotericin B alone (15 vs. 25 deaths by day 14; hazard ratio, 0.57; 95% confidence interval [CI], 0.30 to 1.08; unadjusted P = 0.08; and 30 vs. 44 deaths by day 70; hazard ratio, 0.61; 95% CI, 0.39 to 0.97; unadjusted P = 0.04). Combination therapy with fluconazole had no significant effect on survival, as compared with monotherapy (hazard ratio for death by 14 days, 0.78; 95% CI, 0.44 to 1.41; P = 0.42; hazard ratio for death by 70 days, 0.71; 95% CI, 0.45 to 1.11; P = 0.13). amphotericin B plus flucytosine was associated with significantly increased rates of yeast clearance from cerebrospinal fluid (-0.42 log(10) colony-forming units [CFU] per milliliter per day vs. -0.31 and -0.32 log10 CFU per milliliter per day in groups 1 and 3, respectively; P<0.001 for both comparisons). Rates of adverse events were similar in all groups, although neutropenia was more frequent in patients receiving a combination therapy. CONCLUSIONS amphotericin B plus flucytosine, as compared with amphotericin B alone, is associated with improved survival among patients with cryptococcal meningitis. A survival benefit of amphotericin B plus fluconazole was not found. (Funded by the Wellcome Trust and the British Infection Society; Controlled-Trials.com number, ISRCTN95123928.)
引用
收藏
页码:1291 / 1302
页数:12
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