Micafungin for the prophylaxis and treatment of Candida infections

被引:14
作者
Fritz, Joseph M. [1 ]
Brielmaier, Benjamin D. [1 ,2 ]
Dubberke, Erik R. [1 ]
机构
[1] Washington Univ, Sch Med, Div Infect Dis, Dept Internal Med, St Louis, MO 63110 USA
[2] Univ Chicago, Med Ctr, Chicago, IL 60637 USA
关键词
antifungal; candidiasis; echinocandin; micafungin;
D O I
10.1586/14787210.6.2.153
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Invasive fungal infection is a significant cause of morbidity and mortality worldwide. The incidence of these infections is steadily increasing. In addition, strains resistant to many commonly used antifungal agents are becoming more prevalent. Many new antifungals have become commercially available in recent years, which have vastly improved the ability to treat these infections effectively. Micafungin is one of three commercially available echinocandins available for use in the USA. This class of agents possess a unique mechanism of action that helps to reduce toxicity while maintaining potent antifungal activity. Micafungin is currently approved for the treatment of esophageal candidiasis in adults and is the only in its class approved for the prophylaxis of Candida infection in patients who have undergone hernatopoietic stem cell transplantation. It was also recently approved in the USA for the treatment of candidemia and other forms of invasive candiaisis (acute disseminated candiaisis, Candida peritonitis and abscess). in general, micafungin is well tolerated and has favorable safety and drug-interaction profiles.
引用
收藏
页码:153 / 162
页数:10
相关论文
共 70 条
[41]   Putative role of β-1,3 glucans in Candida albicans biofilm resistance [J].
Nett, Jeniel ;
Lincoln, Leslie ;
Marchillo, Karen ;
Massey, Randall ;
Holoyda, Kathleen ;
Hoff, Brian ;
VanHandel, Michelle ;
Andes, David .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (02) :510-520
[42]   Treatment of Candida glabrata infection in immunosuppressed mice by using a combination of liposomal amphotericin B with caspofungin or micafungin [J].
Olson, JA ;
Adler-Moore, JP ;
Smith, PJ ;
Proffitt, RT .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (12) :4895-4902
[43]   Invasive candidiasis in the intensive care unit [J].
Ostrosky-Zeichner, L ;
Pappas, PG .
CRITICAL CARE MEDICINE, 2006, 34 (03) :857-863
[44]   International, open-label, noncomparative, clinical trial of micafungin alone and in combination for treatment of newly diagnosed and refractory candidemia [J].
Ostrosky-Zeichner, L ;
Kontoyiannis, D ;
Raffalli, J ;
Mullane, KM ;
Vazquez, J ;
Anaissie, EJ ;
Lipton, J ;
Jacobs, P ;
van Rensburg, JHJ ;
Rex, JH ;
Lau, W ;
Facklam, D ;
Buell, DN .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2005, 24 (10) :654-661
[45]   Antifungal susceptibility survey of 2,000 bloodstream Candida isolates in the United States [J].
Ostrosky-Zeichner, L ;
Rex, JH ;
Pappas, PG ;
Hamill, RJ ;
Larsen, RA ;
Horowitz, HW ;
Powderly, WG ;
Hyslop, N ;
Kauffman, CA ;
Cleary, J ;
Mangino, JE ;
Lee, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (10) :3149-3154
[46]   Serum differentially alters the antifungal properties of echinocandin drugs [J].
Paderu, Padmaja ;
Garcia-Effron, Guillermo ;
Balashov, Sergey ;
Delmas, Guillaume ;
Park, Steven ;
Perlin, David S. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (06) :2253-2256
[47]   Micafungin versus caspofungin for treatment of candidemia and other forms of invasive candidiasis [J].
Pappas, Peter G. ;
Rotstein, Coleman M. F. ;
Betts, Robert F. ;
Nucci, Marcio ;
Talwar, Deepak ;
De Waele, Jan J. ;
Vazquez, Jose A. ;
Dupont, Bertrand F. ;
Horn, David L. ;
Ostrosky-Zeichner, Luis ;
Reboli, Annette C. ;
Suh, Byungse ;
Digumarti, Raghunadharao ;
Wu, Chunzhang ;
Kovanda, Laura L. ;
Arnold, Leah J. ;
Buell, Donald N. .
CLINICAL INFECTIOUS DISEASES, 2007, 45 (07) :883-893
[48]   Invasive candidiasis [J].
Pappas, Peter G. .
INFECTIOUS DISEASE CLINICS OF NORTH AMERICA, 2006, 20 (03) :485-+
[49]   Guidelines for treatment of candidiasis [J].
Pappas, PG ;
Rex, JH ;
Sobel, JD ;
Filler, SG ;
Dismukes, WE ;
Walsh, TJ ;
Edwards, JE .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (02) :161-189
[50]   Specific substitutions in the echinocandin target Fks1p account for reduced susceptibility of rare laboratory and clinical Candida sp isolates [J].
Park, S ;
Kelly, R ;
Kahn, JN ;
Robles, J ;
Hsu, MJ ;
Register, E ;
Li, W ;
Vyas, V ;
Fan, H ;
Abruzzo, G ;
Flattery, A ;
Gill, C ;
Chrebet, G ;
Parent, SA ;
Kurtz, A ;
Teppler, H ;
Douglas, CA ;
Perlin, DS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (08) :3264-3273