Isavuconazole in the treatment of invasive aspergillosis and mucormycosis infections

被引:67
作者
Donnelley, Monica A. [1 ,2 ]
Zhu, Elizabeth S. [1 ]
Thompson, George R., III [3 ]
机构
[1] Univ Calif Davis, Dept Inpatient Pharm, Sacramento, CA 95817 USA
[2] Touro Univ, Coll Pharm, Dept Clin Sci, Vallejo, CA USA
[3] Univ Calif Davis, Dept Med, Div Infect Dis, One Shields Ave,Tupper Hall,Rm 3138, Davis, CA 95616 USA
关键词
isavuconazonium; antifungal; zygomycosis; mucor; mold infection; pharmacokinetics; pharmacodynamics; clinical efficacy; therapy; new agent; DRUG-DRUG INTERACTIONS; IN-VITRO ACTIVITY; PHARMACODYNAMIC TARGET DETERMINATION; EPIDEMIOLOGIC CUTOFF VALUES; ORGAN TRANSPLANT RECIPIENTS; ANTIFUNGAL TRIAZOLE BAL4815; CRYPTOCOCCUS-GATTII; FUNGAL-INFECTIONS; SKIN-CANCER; DOSE PHARMACOKINETICS;
D O I
10.2147/IDR.S81416
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
We have a limited arsenal with which to treat invasive fungal infections caused by Aspergillus and Mucorales. The morbidity and mortality for both pathogens remains high. A triazole antifungal, isavuconazole, was recently granted approval by the US Food and Drug Administration and the European Medicines Agency for the treatment of invasive aspergillosis and mucormycosis. A randomized double-blind comparison trial for the treatment of invasive aspergillosis found isavuconazole noninferior to voriconazole. A separate, open-label study evaluating the efficacy of isavuconazole in the treatment of mucormycosis found comparable response rates to amphotericin B and posaconazole treated historical controls. The prodrug isavuconazonium sulfate is commercially available in both an oral and intravenous formulation and is generally well tolerated. Isavuconazole's broad spectrum of activity, limited side effect profile, and favorable pharmacokinetics will likely solidify its place in therapy.
引用
收藏
页码:79 / 86
页数:8
相关论文
共 76 条
[1]   Systemic antifungal agents - Drug interactions of clinical significance [J].
Albengres, E ;
Le Louet, H ;
Tillement, JP .
DRUG SAFETY, 1998, 18 (02) :83-97
[2]   Voriconazole Enhances the Osteogenic Activity of Human Osteoblasts In Vitro through a Fluoride-Independent Mechanism [J].
Allen, Kahtonna C. ;
Sanchez, Carlos J., Jr. ;
Niece, Krista L. ;
Wenke, Joseph C. ;
Akers, Kevin S. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2015, 59 (12) :7205-7213
[3]  
Ananda-Rajah MR, 2015, FUTURE MICROBIOL, V10, P693, DOI [10.2217/FMB.15.34, 10.2217/fmb.15.34]
[4]   Antifungal Therapeutic Drug Monitoring: Established and Emerging Indications [J].
Andes, David ;
Pascual, Andres ;
Marchetti, Oscar .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (01) :24-34
[5]   Impact of Treatment Strategy on Outcomes in Patients with Candidemia and Other Forms of Invasive Candidiasis: A Patient-Level Quantitative Review of Randomized Trials [J].
Andes, David R. ;
Safdar, Nasia ;
Baddley, John W. ;
Playford, Geoffrey ;
Reboli, Annette C. ;
Rex, John H. ;
Sobel, Jack D. ;
Pappas, Peter G. ;
Kullberg, Bart Jan .
CLINICAL INFECTIOUS DISEASES, 2012, 54 (08) :1110-1122
[6]   In Vitro Activity of Isavuconazole and Comparators against Clinical Isolates of the Mucorales Order [J].
Arendrup, Maiken Cavling ;
Jensen, Rasmus Hare ;
Meletiadis, Joseph .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2015, 59 (12) :7735-7742
[7]   Pharmacology of systemic antifungal agents [J].
Ashley, Elizabeth S. Dodds ;
Lewis, Russell ;
Lewis, James S. ;
Martin, Craig ;
Andes, David .
CLINICAL INFECTIOUS DISEASES, 2006, 43 :S28-S39
[8]  
Astellas Pharma US, 2015, PRESCR INF CRES 2015
[9]   Update on rifampin, rifabutin, and rifapentine drug interactions [J].
Baciewicz, Anne M. ;
Chrisman, Cary R. ;
Finch, Christopher K. ;
Self, Timothy H. .
CURRENT MEDICAL RESEARCH AND OPINION, 2013, 29 (01) :1-12
[10]   Clinical impact of drug-drug interactions with systemic azole antifungals [J].
Bates, DW ;
Yu, DT .
DRUGS OF TODAY, 2003, 39 (10) :801-813