A randomized, blinded, multicenter trial of lipid-associated amphotericin B alone versus in combination with an antibody-based inhibitor of heat shock protein 90 in patients with invasive candidiasis

被引:211
作者
Pachl, J
Svoboda, P
Jacobs, F
Vandewoude, K
van der Hoven, B
Spronk, P
Masterson, G
Malbrain, M
Aoun, M
Garbino, J
Takala, J
Drgona, L
Burnie, J
Matthews, R
机构
[1] Res Ctr Traumatol & Surg, Brno, Czech Republic
[2] Charles Univ Prague, Prague, Czech Republic
[3] Erasme Univ Hosp, Brussels, Belgium
[4] Inst Jules Bordet, B-1000 Brussels, Belgium
[5] ZiekenhuisNetwerk Antwerpen Campus Stuivenberg, Antwerp, Belgium
[6] Erasmus Univ, Med Ctr, Rotterdam, Netherlands
[7] Ghent Univ Hosp, B-9000 Ghent, Belgium
[8] Gelre Hosp, Apeldoorn, Netherlands
[9] Univ Liverpool, Liverpool L69 3BX, Merseyside, England
[10] Univ Manchester, Manchester M13 9PL, Lancs, England
[11] NeuTec Pharm, Manchester, Lancs, England
[12] Univ Hosp Geneva, Geneva, Switzerland
[13] Univ Hosp, Bern, Switzerland
[14] NCI, Bratislava, Slovakia
关键词
D O I
10.1086/503428
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Mycograb (NeuTec Pharma) is a human recombinant monoclonal antibody against heat shock protein 90 that, in laboratory studies, was revealed to have synergy with amphotericin B against a broad spectrum of Candida species. Methods. A double-blind, randomized study was conducted to determine whether lipid-associated amphotericin B plus Mycograb was superior to amphotericin B plus placebo in patients with culture-confirmed invasive candidiasis. Patients received a lipid-associated formulation of amphotericin B plus a 5-day course of Mycograb or placebo, having been stratified on the basis of Candida species (Candida albicans vs. non-albicans species of Candida). Inclusion criteria included clinical evidence of active infection at trial entry plus growth of Candida species on culture of a specimen from a clinically significant site within 3 days after initiation of study treatment. The primary efficacy variable was overall response to treatment (clinical and mycological resolution) by day 10. Results. Of the 139 patients enrolled from Europe and the United States, 117 were included in the modified intention-to-treat population. A complete overall response by day 10 was obtained for 29 (48%) of 61 patients in the amphotericin B group, compared with 47 (84%) of 56 patients in the Mycograb combination therapy group (odds ratio [OR], 5.8; 95% confidence interval [CI], 2.41-13.79;). The following efficacy criteria were also met: clinical response (52% vs. 86%; OR, 5.4; 95% CI, 2.21-13.39; P < .001), mycological response (54% vs. 89%; OR, 7.1; 95% CI, 2.64-18.94; P < .001), Candida-attributable mortality (18% vs. 4%; OR, 0.2; 95% CI, 0.04- 0.80; P = .025), and rate of culture-confirmed clearance of the infection (hazard ratio, 2.3; 95% CI, 1.4-3.8; P = .001). Mycograb was well tolerated. Conclusions. Mycograb plus lipid-associated amphotericin B produced significant clinical and culture-confirmed improvement in outcome for patients with invasive candidiasis.
引用
收藏
页码:1404 / 1413
页数:10
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