Division of Hematology/Oncology, University of Florida College of Medicine, P.O. Box 100278, Gainesville, FL, 32610-0278, USA.
Eur J Clin Microbiol Infect Dis. 2010 Nov;29(11):1387-94. doi: 10.1007/s10096-010-1013-0. Epub 2010 Aug 12.
In a non-comparative study, caspofungin was effective salvage therapy for approximately half of the patients refractory to or intolerant of standard antifungal agents for invasive aspergillosis. To establish a frame of reference for these results, we compared the response to caspofungin with responses to other antifungal agents in a historical cohort of similar patients. The efficacy could be evaluated in 83 patients who received caspofungin 50 mg daily after a 70-mg loading dose. The historical control group, identified through a retrospective review of medical records, included 214 evaluable patients possibly refractory to or intolerant of ≥1 week of standard antifungal therapy. All patients had documented invasive aspergillosis. Favorable response was defined as a complete or partial response to therapy. Underlying diseases, baseline neutropenia, corticosteroid use, and sites of infection were similar in both studies. Most patients had received amphotericin B formulations and/or itraconazole, and were refractory to standard therapy. Favorable response rates were 45% with caspofungin and 16% with standard therapy. The unadjusted odds ratio for a favorable response (caspofungin/standard therapy) was 4.1 (95% confidence interval: 2.2, 7.5). After adjusting for potential imbalances in the frequency of disseminated infection, neutropenia, steroid use, and bone marrow transplantation between groups, the odds ratio remained at 4.1 (2.1, 7.9). Although only tentative conclusions about relative efficacy can be drawn from retrospective comparisons, caspofungin appeared to be at least as efficacious as an amphotericin B formulation and/or itraconazole for the treatment of invasive aspergillosis in patients refractory to or intolerant of their initial antifungal therapy.
在一项非对照研究中,卡泊芬净对于大约一半对标准抗真菌药物治疗侵袭性曲霉菌病无效或不耐受的患者是有效的挽救治疗。为了确定这些结果的参考框架,我们将卡泊芬净的疗效与相似患者的历史队列中其他抗真菌药物的疗效进行了比较。在接受 70mg 负荷剂量后,每天给予 50mg 卡泊芬净的 83 例患者中可以评估疗效。通过回顾性病历审查确定的历史对照组包括 214 例可能对标准抗真菌治疗≥1 周无效或不耐受的评估患者。所有患者均有确诊的侵袭性曲霉菌病。疗效定义为治疗的完全或部分反应。在这两项研究中,基础疾病、基线中性粒细胞减少症、皮质类固醇使用和感染部位相似。大多数患者已接受两性霉素 B 制剂和/或伊曲康唑治疗,并且对标准治疗无效。卡泊芬净的缓解率为 45%,标准治疗为 16%。卡泊芬净/标准治疗的有利反应的未调整比值比为 4.1(95%置信区间:2.2,7.5)。在调整组间播散性感染、中性粒细胞减少症、皮质类固醇使用和骨髓移植的频率潜在不平衡后,比值比仍为 4.1(2.1,7.9)。虽然只能从回顾性比较中得出关于相对疗效的暂定结论,但卡泊芬净似乎与两性霉素 B 制剂和/或伊曲康唑一样有效,用于治疗对初始抗真菌治疗无效或不耐受的侵袭性曲霉菌病患者。