Anidulafungin compared with fluconazole for treatment of candidemia and other forms of invasive candidiasis caused by Candida albicans: a multivariate analysis of factors associated with improved outcome

被引:68
作者
Reboli, Annette C. [1 ]
Shorr, Andrew F. [2 ]
Rotstein, Coleman [3 ]
Pappas, Peter G. [4 ]
Kett, Daniel H. [5 ]
Schlamm, Haran T. [6 ]
Reisman, Arlene L. [7 ]
Biswas, Pinaki [8 ]
Walsh, Thomas J. [9 ,10 ]
机构
[1] Rowan Univ, Cooper Med Sch, Div Infect Dis, Camden, NJ 08103 USA
[2] Washington Hosp Ctr, Pulm Crit Care Sect, Washington, DC 20010 USA
[3] Univ Toronto Univ Hlth Network, Div Infect Dis, Toronto, ON, Canada
[4] Univ Alabama Birmingham, Div Infect Dis, Mycoses Study Grp, Birmingham, AL USA
[5] Univ Miami, Miller Sch Med, Dept Clin Med, Miami, FL 33136 USA
[6] Pfizer Inc, Pfizer Specialty Care Antiinfect, New York, NY USA
[7] Pfizer Inc, Pfizer Specialty Care Stat, New York, NY USA
[8] Pfizer Inc, Pfizer Specialty Care Stat, Collegeville, PA USA
[9] Cornell Univ, Weill Cornell Med Coll, Div Infect Dis, New York, NY 10021 USA
[10] New York Presbyterian Hosp, New York, NY USA
关键词
echinocandins; Candida; efficacy; safety; survival; ANTIMICROBIAL SURVEILLANCE PROGRAM; IN-VITRO SUSCEPTIBILITIES; BLOOD-STREAM INFECTIONS; AMPHOTERICIN-B; ECHINOCANDIN LY303366; ANTIFUNGAL AGENTS; UNITED-STATES; EPIDEMIOLOGY; SPP; RESISTANT;
D O I
10.1186/1471-2334-11-261
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Candida albicans is the most common cause of candidemia and other forms of invasive candidiasis. Systemic infections due to C. albicans exhibit good susceptibility to fluconazole and echinocandins. However, the echinocandin anidulafungin was recently demonstrated to be more effective than fluconazole for systemic Candida infections in a randomized, double-blind trial among 245 patients. In that trial, most infections were caused by C. albicans, and all respective isolates were susceptible to randomized study drug. We sought to better understand the factors associated with the enhanced efficacy of anidulafungin and hypothesized that intrinsic properties of the antifungal agents contributed to the treatment differences. Methods: Global responses at end of intravenous study treatment in patients with C. albicans infection were compared post-hoc. Multivariate logistic regression analyses were performed to predict response and to adjust for differences in independent baseline characteristics. Analyses focused on time to negative blood cultures, persistent infection at end of intravenous study treatment, and 6-week survival. Results: In total, 135 patients with C. albicans infections were identified. Among these, baseline APACHE II scores were similar between treatment arms. In these patients, global response was significantly better for anidulafungin than fluconazole (81.1% vs 62.3%; 95% confidence interval [CI] for difference, 3.7-33.9). After adjusting for baseline characteristics, the odds ratio for global response was 2.36 (95% CI, 1.06-5.25). Study treatment and APACHE II score were significant predictors of outcome. The most predictive logistic regression model found that the odds ratio for study treatment was 2.60 (95% CI, 1.14-5.91) in favor of anidulafungin, and the odds ratio for APACHE II score was 0.935 (95% CI, 0.885-0.987), with poorer responses associated with higher baseline APACHE II scores. Anidulafungin was associated with significantly faster clearance of blood cultures (log-rank p < 0.05) and significantly fewer persistent infections (2.7% vs 13.1%; p < 0.05). Survival through 6 weeks did not differ between treatment groups. Conclusions: In patients with C. albicans infection, anidulafungin was more effective than fluconazole, with more rapid clearance of positive blood cultures. This suggests that the fungicidal activity of echinocandins may have important clinical implications.
引用
收藏
页数:8
相关论文
共 39 条
[1]   NEW LOOK AT STATISTICAL-MODEL IDENTIFICATION [J].
AKAIKE, H .
IEEE TRANSACTIONS ON AUTOMATIC CONTROL, 1974, AC19 (06) :716-723
[2]   LYSIS CENTRIFUGATION BLOOD CULTURES IN THE DETECTION OF TISSUE-PROVEN INVASIVE CANDIDIASIS - DISSEMINATED VERSUS SINGLE-ORGAN INFECTION [J].
BERENGUER, J ;
BUCK, M ;
WITEBSKY, F ;
STOCK, F ;
PIZZO, PA ;
WALSH, TJ .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1993, 17 (02) :103-109
[3]   High dissemination and hepatotoxicity in rats infected with Candida albicans after stress exposure:: potential sensitization to liver damage [J].
Correa, SG ;
Rodríguez-Galán, MC ;
Salido-Rentería, B ;
Cano, R ;
Cejas, H ;
Sotomayor, CE .
INTERNATIONAL IMMUNOLOGY, 2004, 16 (12) :1761-1768
[4]   Susceptibility of fluconazole-resistant clinical isolates of Candida spp. to echinocandin LY303366, itraconazole and amphotericin B [J].
Cuenca-Estrella, M ;
Mellado, E ;
Díaz-Guerra, TM ;
Monzón, A ;
Rodríguez-Tudela, JL .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2000, 46 (03) :475-477
[5]   Anidulafungin: a new echinocandin for candidal infections [J].
de la Torre, Polo ;
Reboli, Annette C. .
EXPERT REVIEW OF ANTI-INFECTIVE THERAPY, 2007, 5 (01) :45-52
[6]   Epidemiology of candidemia: 3-year results from the emerging infections and the epidemiology of Iowa organisms study [J].
Diekema, DJ ;
Messer, SA ;
Brueggemann, AB ;
Coffman, SL ;
Doern, GV ;
Herwaldt, LA ;
Pfaller, MA .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (04) :1298-1302
[7]   Anidulafungin does not require dosage adjustment in subjects with varying degrees of hepatic or renal impairment [J].
Dowell, James A. ;
Stogniew, Martin ;
Krause, David ;
Damle, Bharat .
JOURNAL OF CLINICAL PHARMACOLOGY, 2007, 47 (04) :461-470
[8]  
Espinel-Ingroff Ana, 2003, Revista Iberoamericana de Micologia, V20, P121
[9]   Candida albicans RFX2 Encodes a DNA Binding Protein Involved in DNA Damage Responses, Morphogenesis, and Virulence [J].
Hao, Binghua ;
Clancy, Cornelius J. ;
Cheng, Shaoji ;
Raman, Suresh B. ;
Iczkowski, Kenneth A. ;
Nguyen, M. Hong .
EUKARYOTIC CELL, 2009, 8 (04) :627-639
[10]   Pharmacokinetics of micafungin in healthy volunteers, volunteers with moderate liver disease, and volunteers with renal dysfunction [J].
Hebert, MF ;
Smith, HE ;
Marbury, TC ;
Swan, SK ;
Smith, WB ;
Townsend, RW ;
Buell, D ;
Keirns, J ;
Bekersky, I .
JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 45 (10) :1145-1152