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伊曲康唑治疗真菌病。

Treatment of mycoses with itraconazole.

作者信息

Tucker R M, Williams P L, Arathoon E G, Stevens D A

机构信息

Department of Medicine, Santa Clara Valley Medical Center, San Jose, California 95128.

出版信息

Ann N Y Acad Sci. 1988;544:451-70. doi: 10.1111/j.1749-6632.1988.tb40443.x.

Abstract

The efficacy of itraconazole, a new oral triazole, was evaluated at doses of 50-400 mg/day in 64 courses: 39 with coccidioidomycosis, and 25 with other mycoses. Among patients with coccidioidomycosis, 21 had pulmonary disease; 10, bone and joint; 8, lymphatic; 6, skin and soft tissue; 3, meningeal; and 1, urogenital. After a mean of 7.1 months of treatment, 17 of 27 evaluable courses (63%) have shown a full response; 8 (30%), a partial response; and 2 (7%), no response. Response to treatment was higher in patients with a shorter duration of illness and in patients with no previous treatment. After a mean of 12 months of treatment, two of five responders off therapy have relapsed. In patients with other mycoses, diagnoses include aspergillosis in six patients; histoplasmosis and tinea in three each; alternariosis, candidiasis, cryptococcosis, blastomycosis, and chromomycosis in two each; and pseudallescheriosis in one. After a mean of 9.4 months of treatment, 14 of 23 evaluable patients (61%) have shown a full response; 2 (8%), a partial response; and 7 (30%), no response. All patients with histoplasmosis and blastomycosis have responded to therapy. There are no relapses among five evaluable responders after a mean of 9.2 months off therapy. In 512 patient months of therapy, toxicity has been minimal. Mean serum levels in patients receiving 200 mg twice daily range from 3.9 to 5.9 micrograms/ml for 8 hr after dosing, with a peak at 7 hr and wide interpatient variability. Itraconazole is well tolerated and has continued to demonstrate efficacy in the treatment of a variety of systemic and superficial mycoses.

摘要

对一种新型口服三唑类药物伊曲康唑进行了评估,其剂量为每日50 - 400毫克,共64个疗程:39例用于球孢子菌病,25例用于其他真菌病。在球孢子菌病患者中,21例患有肺部疾病;10例患有骨与关节疾病;8例患有淋巴系统疾病;6例患有皮肤和软组织疾病;3例患有脑膜疾病;1例患有泌尿生殖系统疾病。经过平均7.1个月的治疗,27个可评估疗程中有17个(63%)显示完全缓解;8个(30%)部分缓解;2个(7%)无反应。病程较短且未接受过先前治疗的患者对治疗的反应更高。经过平均12个月的治疗,5名停止治疗的缓解患者中有2名复发。在患有其他真菌病的患者中,诊断包括6例曲霉病;3例组织胞浆菌病和3例癣;2例链格孢菌病、念珠菌病、隐球菌病、芽生菌病和着色芽生菌病;1例假阿利什霉病。经过平均9.4个月的治疗,23名可评估患者中有14名(61%)显示完全缓解;2名(8%)部分缓解;7名(30%)无反应。所有组织胞浆菌病和芽生菌病患者对治疗均有反应。平均停药9.2个月后,5名可评估的缓解患者中无复发情况。在512个患者治疗月中,毒性极小。接受每日两次200毫克治疗的患者,给药后8小时血清平均水平为3.9至5.9微克/毫升,7小时达到峰值,患者间差异较大。伊曲康唑耐受性良好,并且在治疗各种系统性和浅表真菌病方面持续显示出疗效。

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