医学
伏立康唑
内科学
茴香菌素
联合疗法
曲菌病
人口
抗真菌
安慰剂
随机对照试验
析因分析
外科
胃肠病学
卡斯波芬金
免疫学
病理
替代医学
环境卫生
皮肤病科
作者
Kieren A. Marr,Haran T. Schlamm,Raoul Herbrecht,Scott T. Rottinghaus,Eric J. Bow,Oliver A. Cornely,Werner Heinz,Shyla Jagannatha,Liang Piu Koh,Dimitrios P. Kontoyiannis,Dong‐Gun Lee,Márcio Nucci,Peter G. Pappas,Monica A. Slavin,Flávio Queiroz‐Telles,Dominik Selleslag,Thomas J. Walsh,John R. Wingard,Johan Maertens
摘要
This article has been corrected. The original version (PDF) is appended to this article as a Supplement. Background: Invasive aspergillosis (IA) is associated with poor outcomes in patients with hematologic malignancies (HMs) and hematopoietic cell transplantation (HCT). Small studies suggest a role for combination antifungal therapy. Objective: To assess the safety and efficacy of voriconazole and anidulafungin compared with voriconazole monotherapy for treatment of IA. Design: Randomized, double-blind, placebo-controlled multicenter trial. (ClinicalTrials.gov: NCT00531479) Setting: 93 international sites. Patients: 454 patients with HM or HCT and suspected or documented IA were randomly assigned to treatment with voriconazole and anidulafungin or placebo. Primary analysis was done in the modified intention-to-treat population of 277 patients in whom IA was confirmed. Measurements: The primary outcome was 6-week mortality; secondary outcomes included 12-week mortality, mortality in major subgroups, and safety measures. Results: Mortality rates at 6 weeks were 19.3% (26 of 135) for combination therapy and 27.5% (39 of 142) for monotherapy (difference, −8.2 percentage points [95% CI, −19.0 to 1.5]; P = 0.087). Secondary mortality outcomes favored combination therapy. Multivariable regression analysis suggested that maximum galactomannan value, Karnofsky score, and baseline platelet count had prognostic significance. Most patients (218 of 277 [78.7%]) had IA diagnosis established by radiographic findings and maximum galactomannan positivity. In a post hoc analysis of this dominant subgroup, 6-week mortality was lower in combination therapy than monotherapy (15.7% [17 of 108] vs. 27.3% [30 of 110]; difference, −11.5 percentage points [CI, −22.7 to −0.4]; P = 0.037). Safety measures, including hepatotoxicity, were not different. Limitations: Mortality at 6 weeks was higher than expected, and the difference in mortality was lower than expected, which reduced power to detect a treatment effect. Enrollment was restricted to patients with HM or HCT, which limited generalizability. Conclusion: Compared with voriconazole monotherapy, combination therapy with anidulafungin led to higher survival in subgroups of patients with IA. Limitations in power preclude definitive conclusions about superiority. Primary Funding Source: Pfizer.
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