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美国国立过敏与传染病研究所真菌病研究组侵袭性曲霉病口服伊曲康唑治疗的多中心试验

NIAID Mycoses Study Group Multicenter Trial of Oral Itraconazole Therapy for Invasive Aspergillosis.

作者信息

Denning D W, Lee J Y, Hostetler J S, Pappas P, Kauffman C A, Dewsnup D H, Galgiani J N, Graybill J R, Sugar A M, Catanzaro A

机构信息

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

出版信息

Am J Med. 1994 Aug;97(2):135-44. doi: 10.1016/0002-9343(94)90023-x.

Abstract

BACKGROUND

Invasive aspergillosis is the most common invasive mould infection and a major cause of mortality in immunocompromised patients. Response to amphotericin B, the only antifungal agent licensed in the United States for the treatment of aspergillosis, is suboptimal.

METHODS

A multicenter open study with strict entry criteria for invasive aspergillosis evaluated oral itraconazole (600 mg/d for 4 days followed by 400 mg/d) in patients with various underlying conditions. Response was based on clinical and radiologic criteria plus microbiology, histopathology, and autopsy data. Responses were categorized as complete, partial, or stable. Failure was categorized as an itraconazole failure or overall failure.

RESULTS

Our study population consisted of 76 evaluable patients. Therapy duration varied from 0.3 to 97 weeks (median 46). At the end of treatment, 30 (39%) patients had a complete or partial response, and 3 (4%) had a stable response, and in 20 patients (26%), the protocol therapy was discontinued early (at 0.6 to 54.3 weeks) because of a worsening clinical course or death due to aspergillosis (itraconazole failure). Twenty-three (30%) patients withdrew for other reasons including possible toxicity (7%) and death due to another cause but without resolution of aspergillosis (20%). Itraconazole failure rates varied widely according to site of disease and underlying disease group: 14% for pulmonary and tracheobronchial disease, 50% for sinus disease, 63% for central nervous system disease, and 44% for other sites; 7% in solid organ transplant, 29% in allogeneic bone marrow transplant patients, and 14% in those with prolonged granulocytopenia (median 19 days), 44% in AIDS patients, and 32% in other host groups. The relapse rates among those who completed therapy and those who discontinued early for possible toxicity were 12% and 40%, respectively; all were still immunosuppressed.

CONCLUSION

Oral itraconazole is a useful alternative therapy for invasive aspergillosis with response rates apparently comparable to amphotericin B. Relapse in immunocompromised patients may be a problem. Controlled trials are necessary to fully assess the role of itraconazole in the treatment of invasive aspergillosis.

摘要

背景

侵袭性曲霉病是最常见的侵袭性霉菌感染,也是免疫功能低下患者死亡的主要原因。对于美国唯一获批用于治疗曲霉病的抗真菌药物两性霉素B,其治疗效果并不理想。

方法

一项针对侵袭性曲霉病制定严格入选标准的多中心开放性研究,评估了口服伊曲康唑(第1天至第4天600mg/天,之后400mg/天)对各种基础疾病患者的疗效。疗效基于临床和影像学标准,以及微生物学、组织病理学和尸检数据。疗效分为完全缓解、部分缓解或病情稳定。治疗失败分为伊曲康唑治疗失败或总体治疗失败。

结果

我们的研究对象包括76例可评估患者。治疗时间从0.3周至97周不等(中位数为46周)。治疗结束时,30例(39%)患者完全或部分缓解,3例(4%)患者病情稳定,20例(26%)患者因临床病程恶化或死于曲霉病(伊曲康唑治疗失败)而在0.6周至54.3周提前终止方案治疗。23例(30%)患者因其他原因退出,包括可能的毒性反应(7%)以及死于其他原因但曲霉病未缓解(20%)。伊曲康唑治疗失败率因疾病部位和基础疾病组的不同而有很大差异:肺部和气管支气管疾病为14%,鼻窦疾病为50%,中枢神经系统疾病为63%,其他部位为44%;实体器官移植患者为7%,异基因骨髓移植患者为29%,粒细胞缺乏持续时间较长(中位数19天)的患者为14%,艾滋病患者为44%,其他宿主组为32%。完成治疗的患者和因可能的毒性反应提前停药的患者的复发率分别为12%和40%;所有患者仍处于免疫抑制状态。

结论

口服伊曲康唑是侵袭性曲霉病的一种有效替代疗法,其有效率与两性霉素B相当。免疫功能低下患者的复发可能是一个问题。需要进行对照试验以全面评估伊曲康唑在侵袭性曲霉病治疗中的作用。

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