McKinsey D S, Wheat L J, Cloud G A, Pierce M, Black J R, Bamberger D M, Goldman M, Thomas C J, Gutsch H M, Moskovitz B, Dismukes W E, Kauffman C A
University of Missouri-Kansas City School of Medicine, and Kansas City AIDS Research Consortium, USA.
Clin Infect Dis. 1999 May;28(5):1049-56. doi: 10.1086/514744.
In a prospective, randomized, double-blind trial, 149 patients with advanced human immunodeficiency virus (HIV) infection were randomized to receive itraconazole capsules (200 mg daily) and 146 to receive a matched placebo. Both groups were monitored for evidence of fungal infections. Baseline characteristics of the two groups were similar. Failure of prophylaxis occurred in 29 (19%) of the itraconazole recipients and 42 (29%) of the placebo recipients (P = .004; log-rank test). There were 6 invasive fungal infections in the itraconazole group (4, histoplasmosis; 1, cryptococcosis; 1, aspergillosis) and 19 in the placebo group (10, histoplasmosis; 8, cryptococcosis; 1, aspergillosis) (P = .0007; log-rank test). Itraconazole significantly delayed time to onset of histoplasmosis (P = .03; log-rank test) and cryptococcosis (P = .0005; log-rank test). Prophylaxis failure due to recurrent or refractory mucosal candidiasis occurred with similar frequency in the two groups (itraconazole, 15%; placebo, 16%). A survival benefit was not demonstrated. Itraconazole generally was well tolerated. Primary prophylaxis with itraconazole capsules prevents histoplasmosis and cryptococcosis in patients with HIV infection.
在一项前瞻性、随机、双盲试验中,149例晚期人类免疫缺陷病毒(HIV)感染患者被随机分配接受伊曲康唑胶囊(每日200毫克),146例接受匹配的安慰剂。两组均监测真菌感染证据。两组的基线特征相似。伊曲康唑治疗组中有29例(19%)预防失败,安慰剂治疗组中有42例(29%)预防失败(P = 0.004;对数秩检验)。伊曲康唑组有6例侵袭性真菌感染(4例组织胞浆菌病;1例隐球菌病;1例曲霉病),安慰剂组有19例(10例组织胞浆菌病;8例隐球菌病;1例曲霉病)(P = 0.0007;对数秩检验)。伊曲康唑显著延迟了组织胞浆菌病(P = 0.03;对数秩检验)和隐球菌病(P = 0.0005;对数秩检验)的发病时间。两组中因复发性或难治性黏膜念珠菌病导致的预防失败发生率相似(伊曲康唑组为15%;安慰剂组为16%)。未显示出生存获益。伊曲康唑总体耐受性良好。伊曲康唑胶囊进行一级预防可预防HIV感染患者的组织胞浆菌病和隐球菌病。