Combination chemotherapy for invasive fungal infections: what laboratory and clinical studies tell us so far

被引:47
作者
Kontoyiannis, DP
Lewis, RE
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Infect Dis, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Infect Control, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Employee Hlth, Houston, TX 77030 USA
[4] Univ Houston, Coll Pharm, Houston, TX 77030 USA
关键词
combination chemotherapy; antifungal; synergy; aspergillosis; candidiasis;
D O I
10.1016/j.drup.2003.08.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite potential benefits, few objective clinical data (with the exception of cryptococcocal meningitis) are available supporting the routine use of combination antifungal regimens in patients with invasive mycoses, importantly aspergillosis or candidiasis. There is considerable debate on what constitutes synergy or antagonism in vitro and whether these laboratory findings are translated to beneficial interactions in patients. Given the lack of rigorous clinical data, a better understanding of the important concepts for the justification of the clinical and pharmacoeconomic threshold of antifungal therapy is needed. Such concepts include standardized methods for screening antifungal combinations in culture or in animals and collaborative efforts to collect clinical data on the efficacy and safety of combination regimens. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:257 / 269
页数:13
相关论文
共 75 条
[1]   Refractory aspergillus pneumonia in patients with acute leukemia - Successful therapy with combination caspofungin and liposomal amphotericin [J].
Aliff, TB ;
Maslak, PG ;
Jurcic, JG ;
Heaney, ML ;
Cathcart, KN ;
Sepkowitz, KA ;
Weiss, MA .
CANCER, 2003, 97 (04) :1025-1032
[2]   Pharmacodynamics of amphotericin B in a neutropenic-mouse disseminated-candidiasis model [J].
Andes, D ;
Stamsted, T ;
Conklin, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (03) :922-926
[3]   Candidemia in a tertiary care cancer center - In vitro susceptibility and its association with outcome of initial antifungal therapy [J].
Antoniadou, A ;
Torres, HA ;
Lewis, RE ;
Thornby, J ;
Bodey, GP ;
Tarrand, JJ ;
Han, XY ;
Rolston, KVI ;
Safdar, A ;
Raad, II ;
Kontoyiannis, DP .
MEDICINE, 2003, 82 (05) :309-321
[4]   Interactions between triazoles and amphotericin B against Cryptococcus neoformans [J].
Barchiesi, F ;
Schimizzi, AM ;
Caselli, F ;
Novelli, A ;
Fallani, S ;
Giannini, D ;
Arzeni, D ;
Di Cesare, S ;
Di Francesco, LF ;
Fortuna, M ;
Giacometti, A ;
Carle, F ;
Mazzei, T ;
Scalise, G .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (09) :2435-2441
[5]   COMPARISON OF AMPHOTERICIN-B ALONE AND COMBINED WITH FLUCYTOSINE IN THE TREATMENT OF CRYPTOCCAL MENINGITIS [J].
BENNETT, JE ;
DISMUKES, WE ;
DUMA, RJ ;
MEDOFF, G ;
SANDE, MA ;
GALLIS, H ;
LEONARD, J ;
FIELDS, BT ;
BRADSHAW, M ;
HAYWOOD, H ;
MCGEE, ZA ;
CATE, TR ;
COBBS, CG ;
WARNER, JF ;
ALLING, DW .
NEW ENGLAND JOURNAL OF MEDICINE, 1979, 301 (03) :126-131
[6]  
BOKTOUR MR, 2003, 41 INF DIS SOC AM ID
[7]   The antifungal echinocandin caspofungin acetate kills growing cells of Aspergillus fumigatus in vitro [J].
Bowman, JC ;
Hicks, PS ;
Kurtz, MB ;
Rosen, H ;
Schmatz, DM ;
Liberator, PA ;
Douglas, CM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (09) :3001-3012
[8]   TISSUE CONCENTRATIONS AND BIOACTIVITY OF AMPHOTERICIN-B IN CANCER-PATIENTS TREATED WITH AMPHOTERICIN-B-DEOXYCHOLATE [J].
COLLETTE, N ;
VANDERAUWERA, P ;
LOPEZ, AP ;
HEYMANS, C ;
MEUNIER, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (03) :362-368
[9]  
COZENS RM, 1999, HDB ANIMAL MODELS IF
[10]   ITRACONAZOLE COMPARED WITH AMPHOTERICIN-B PLUS FLUCYTOSINE IN AIDS PATIENTS WITH CRYPTOCOCCAL MENINGITIS [J].
DEGANS, J ;
PORTEGIES, P ;
TIESSENS, G ;
SCHATTENKERK, JKME ;
VANBOXTEL, CJ ;
VANKETEL, RJ ;
STAM, J .
AIDS, 1992, 6 (02) :185-190