Wheat J, Hafner R, Korzun A H, Limjoco M T, Spencer P, Larsen R A, Hecht F M, Powderly W
Department of Medicine, Indiana University, Indianapolis, USA.
Am J Med. 1995 Apr;98(4):336-42. doi: 10.1016/s0002-9343(99)80311-8.
Amphotericin B has been the treatment of choice for disseminated histoplasmosis in patients with acquired immunodeficiency syndrome (AIDS). Oral antifungal agents would be welcome alternatives to standard treatment of disseminated histoplasmosis in less severe cases. The purpose of this study was to assess the efficacy and safety of itraconazole therapy in patients with AIDS and disseminated histoplasmosis.
This was a multicenter, open-label, nonrandomized prospective trial conducted in university hospitals of the AIDS Clinical Trial Group. All patients had AIDS and first episodes of disseminated histoplasmosis. Patients with central nervous system involvement or with severe clinical manifestations were excluded. Patients were treated with itraconazole BID by mouth 300 mg for 3 days and then 200 mg BID for 12 weeks. Resolution of clinical findings, clearance of positive cultures, and drug tolerance were the main outcome measurements. A secondary objective was effect of therapy on Histoplasma capsulatum var capsulatum antigen levels.
Of 59 evaluable patients, 50 (85%) responded to therapy. Five patients withdrew because of progressive infection, 1 died of a presumed pulmonary embolus within the first week of therapy without improvement, 2 withdrew because of toxicity, and 1 was lost to follow-up after week 2 of therapy. Patients with moderately severe clinical (fever > 39.5 degrees C or Karnofsky score < 60) or laboratory abnormalities (alkaline phosphatase > 5 times normal or albumin < 3 g/dL) at baseline tended to respond more poorly than did other patients. Resolution of complaints of fever and improvement in fatigue occurred after a median of 3 and 6 weeks, respectively, and weight gain after 2 weeks. Fungemia cleared after a median of 1 week. H capsulatum var capsulatum antigen cleared from the urine and serum at rates of 0.2 and 0.3 units per week, respectively.
Itraconazole is safe and effective induction therapy for mild disseminated histoplasmosis in patients with AIDS, offering an alternative to amphotericin B in such cases. Patients with moderately severe or severe histoplasmosis should first be treated with amphotericin B and then may be switched to itraconazole after achieving clinical improvement.
两性霉素B一直是获得性免疫缺陷综合征(AIDS)患者播散性组织胞浆菌病的首选治疗药物。在病情较轻的播散性组织胞浆菌病患者中,口服抗真菌药物将是标准治疗的理想替代方案。本研究的目的是评估伊曲康唑治疗AIDS合并播散性组织胞浆菌病患者的疗效和安全性。
这是一项在艾滋病临床试验组大学医院进行的多中心、开放标签、非随机前瞻性试验。所有患者均患有AIDS且为播散性组织胞浆菌病首次发作。排除有中枢神经系统受累或有严重临床表现的患者。患者口服伊曲康唑,每日两次,300mg,共3天,然后每日两次,200mg,共12周。临床症状的缓解、阳性培养结果的清除和药物耐受性是主要的观察指标。次要目标是治疗对荚膜组织胞浆菌荚膜变种抗原水平的影响。
59例可评估患者中,50例(85%)对治疗有反应。5例患者因感染进展而退出,1例在治疗第一周内死于疑似肺栓塞且病情无改善,2例因毒性反应退出,1例在治疗第2周后失访。基线时具有中度严重临床症状(发热>39.5℃或卡诺夫斯基评分<60)或实验室异常(碱性磷酸酶>正常上限5倍或白蛋白<3g/dL)的患者,其反应往往比其他患者差。发热症状的缓解和疲劳的改善分别在中位时间3周和6周后出现,体重在2周后增加。真菌血症在中位时间1周后清除。荚膜组织胞浆菌荚膜变种抗原分别以每周0.2和0.3单位的速率从尿液和血清中清除。
伊曲康唑是治疗AIDS患者轻度播散性组织胞浆菌病的安全有效的诱导治疗药物,在此类病例中可作为两性霉素B的替代药物。中度严重或严重组织胞浆菌病患者应首先用两性霉素B治疗,在临床症状改善后可改用伊曲康唑。