Wheat L J, Connolly P, Smedema M, Brizendine E, Hafner R
Indiana University School of Medicine, Histoplasmosis Reference Laboratory, and Veterans' Affairs Medical Center, Indianapolis, IN 46202, USA.
Clin Infect Dis. 2001 Dec 1;33(11):1910-3. doi: 10.1086/323781. Epub 2001 Oct 23.
In sequential clinical trials of treatment for histoplasmosis in patients with acquired immunodeficiency syndrome, therapy with fluconazole failed in a higher proportion of patients than did therapy with itraconazole. To determine the cause for failure with fluconazole, antifungal susceptibility testing that used modified National Committee on Clinical Laboratory Standards procedures was performed on all baseline and failure isolates. Failure occurred more frequently in patients with baseline isolates with fluconazole minimum inhibitory concentrations (MICs) > or =5 microg/mL versus lower MICs; 29% versus 3%, respectively. There was at least a 4-fold increase in fluconazole MIC in the isolates from 10 (59%) of 17 patients for whom paired pretreatment and failure or relapse isolates were available. Cross-resistance to itraconazole was not seen. In conclusion, fluconazole is less active than itraconazole for Histoplasma capsulatum and induces resistance during therapy, which accounted for treatment failure in some patients.
在获得性免疫缺陷综合征患者组织胞浆菌病治疗的序贯临床试验中,氟康唑治疗失败的患者比例高于伊曲康唑治疗。为确定氟康唑治疗失败的原因,对所有基线和治疗失败时的分离株采用改良的美国国家临床实验室标准委员会程序进行抗真菌药敏试验。与氟康唑最低抑菌浓度(MIC)<5μg/mL的基线分离株相比,MIC≥5μg/mL的基线分离株患者治疗失败更为频繁,分别为29%和3%。在17例有配对的治疗前和治疗失败或复发分离株的患者中,10例(59%)患者的分离株中氟康唑MIC至少增加了4倍。未发现对伊曲康唑的交叉耐药。总之,氟康唑对荚膜组织胞浆菌的活性低于伊曲康唑,且在治疗过程中可诱导耐药,这是部分患者治疗失败的原因。