Caspofungin - A review of its use in oesophageal candidiasis, invasive candidiasis and invasive aspergillosis

被引:55
作者
Keating, GM [1 ]
Figgitt, DP [1 ]
机构
[1] Adis Int Ltd, Auckland 1311, New Zealand
关键词
caspofungin; invasive aspergillosis; oesophageal candidiasis; invasive candidiasis; pharmacodynamics; pharmacokinetics; therapeutic use;
D O I
10.2165/00003495-200363200-00008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Echinocandins are a new class of antifungal agents with a novel mechanism of action (interference with fungal-cell wall synthesis). Caspofungin (Cancidas(R), Caspofungin MSD(R)) is the first echinocandin to be approved and is administered intravenously. Caspofungin 50 mg/day had similar efficacy to intravenous fluconazole 200 mg/day and was at least as effective as intravenous amphotericin B 0.5 mg/kg/day in patients with oesophageal candidiasis in two randomised, double-blind studies. A favourable combined clinical and endoscopic response occurred in 81% of caspofungin recipients versus 85% of fluconazole recipients and in 74% of caspofungin recipients versus 63% of amphotericin B recipients. A favourable combined response rate of approximate to90% and approximate to60% occurred in the stratum of patients with oesophageal candidiasis who received caspofungin or amphotericin B in a third randomised, double-blind study. Caspofungin (70mg loading dose followed by 50 mg/day) had similar efficacy to intravenous amphotericin B (0.7-1.0 mg/kg/day in patients with neutropenia and 0.6-0.7 mg/kg/day in patients without neutropenia) in patients with invasive candidiasis in a double-blind, randomised trial. A favourable overall response occurred in 73.4% of caspofungin recipients and in 61.7% of amphotericin B recipients. In a noncomparative study, salvage therapy with caspofungin (70mg loading dose followed by 50 mg/day) was effective in patients with invasive aspergillosis who were refractory to or did not tolerate standard antifungal therapy. A favourable response (complete plus partial response) occurred in 37 of 83 patients (45%). Caspofungin was generally well tolerated in clinical trials; it had similar tolerability to intravenous fluconazole and was better tolerated than intravenous amphotericin B. Significantly fewer caspofungin than amphotericin B recipients reported chills, fever, nausea or infusion-related adverse events. In conclusion, caspofungin is a valuable new antifungal agent with a novel mechanism of action. In comparative trials, caspofungin had similar efficacy to fluconazole and was at least as effective as. amphotericin B in oesophageal candidiasis and had similar efficacy to amphotericin B in invasive candidiasis. In addition, caspofungin had similar tolerability to fluconazole and was better tolerated than amphotericin B in these indications. Caspofungin was also effective in patients with invasive aspergillosis who were refractory to or intolerant of standard antifungal. agents. Thus, caspofungin provides an alternative to triazoles or amphotericin B in oesophageal. candidiasis and an alternative to amphotericin B in invasive candidiasis, as well as being an effective salvage therapy in invasive aspergillosis.
引用
收藏
页码:2235 / 2263
页数:29
相关论文
共 112 条
[1]   Efficacy of the echinocandin caspofungin against disseminated aspergillosis and candidiasis in cyclophosphamide-induced immunosuppressed mice [J].
Abruzzo, GK ;
Gill, CJ ;
Flattery, AM ;
Kong, L ;
Leighton, C ;
Smith, JG ;
Pikounis, VB ;
Bartizal, K ;
Rosen, H .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (09) :2310-2318
[2]   Evaluation of the echinocandin antifungal MK-0991 (L-743,872): Efficacies in mouse models of disseminated aspergillosis, candidiasis, and cryptococcosis [J].
Abruzzo, GK ;
Flattery, AM ;
Gill, CJ ;
Kong, L ;
Smith, JG ;
Pikounis, VB ;
Balkovec, JM ;
Bouffard, AF ;
Dropinski, JF ;
Rosen, H ;
Kropp, H ;
Bartizal, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (11) :2333-2338
[3]   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
[4]   Randomized, double-blind, Multicenter study of caspofungin versus amphotericin B for treatment of oropharyngeal and esophageal candidiases [J].
Arathoon, EG ;
Gotuzzo, E ;
Noriega, LM ;
Berman, RS ;
DiNubile, MJ ;
Sable, CA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (02) :451-457
[5]  
Arikan S., 2002, International Journal of Antimicrobial Agents, V19, pS75
[6]   Comparative evaluation of disk diffusion with microdilution assay in susceptibility testing of caspofungin against Aspergillus and Fusarium isolates [J].
Arikan, S ;
Paetznick, V ;
Rex, JH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (09) :3084-3087
[7]   In vitro synergy of caspofungin and amphotericin B against Aspergillus and Fusarium spp. [J].
Arikan, S ;
Lozano-Chiu, M ;
Paetznick, V ;
Rex, JH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (01) :245-247
[8]   In vitro susceptibility testing methods for caspofungin against Aspergillus and Fusarium isolates [J].
Arikan, S ;
Lozano-Chiu, M ;
Paetznick, V ;
Rex, JH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (01) :327-330
[9]   In vitro activity of caspofungin (MK-0991) against Candida albicans clinical isolates displaying different mechanisms of azole resistance [J].
Bachmann, SP ;
Patterson, TF ;
López-Ribot, JL .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (06) :2228-2230
[10]  
Balani SK, 2000, DRUG METAB DISPOS, V28, P1274