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首页> 外文期刊>The Lancet >Micafungin versus liposomal amphotericin B for candidaemia and invasive candidosis: a phase III randomised double-blind trial.
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Micafungin versus liposomal amphotericin B for candidaemia and invasive candidosis: a phase III randomised double-blind trial.

机译:米卡芬净与脂质体两性霉素B治疗念珠菌血症和侵袭性念珠菌病:III期随机双盲试验。

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BACKGROUND: Invasive candidosis is increasingly prevalent in seriously ill patients. Our aim was to compare micafungin with liposomal amphotericin B for the treatment of adult patients with candidaemia or invasive candidosis. METHODS: We did a double-blind, randomised, multinational non-inferiority study to compare micafungin (100 mg/day) with liposomal amphotericin B (3 mg/kg per day) as first-line treatment of candidaemia and invasive candidosis. The primary endpoint was treatment success, defined as both a clinical and a mycological response at the end of treatment. Primary analyses were done on a per-protocol basis. This trial is registered with ClinicalTrials.gov, number NCT00106288. FINDINGS: 264 individuals were randomly assigned to treatment with micafungin; 267 were randomly assigned to receive liposomal amphotericin B. 202 individuals in the micafungin group and 190 in the liposomal amphotericin B group were included in the per-protocol analyses. Treatment success was observed for 181 (89.6%)patients treated with micafungin and 170 (89.5%) patients treated with liposomal amphotericin B. The difference in proportions, after stratification by neutropenic status at baseline, was 0.7% (95% CI -5.3 to 6.7). Efficacy was independent of the Candida spp and primary site of infection, as well as neutropenic status, APACHE II score, and whether a catheter was removed or replaced during the study. There were fewer treatment-related adverse events--including those that were serious or led to treatment discontinuation--with micafungin than there were with liposomal amphotericin B. INTERPRETATION: Micafungin was as effective as--and caused fewer adverse events than--liposomal amphotericin B as first-line treatment of candidaemia and invasive candidosis.
机译:背景:侵袭性念珠菌病在重症患者中越来越普遍。我们的目的是比较米卡芬净与脂质体两性霉素B在成人念珠菌血症或浸润性念珠菌病患者中的治疗效果。方法:我们进行了一项双盲,随机,多国非劣效性研究,以比较米卡芬净(100毫克/天)和脂质体两性霉素B(3毫克/千克/天)作为念珠菌血症和浸润性念珠菌病的一线治疗。主要终点是治疗成功,定义为治疗结束时的临床反应和真菌反应。初步分析是按协议进行的。该试验已在ClinicalTrials.gov上注册,编号为NCT00106288。结果:264名患者被随机分配接受米卡芬净治疗; 267人被随机分配接受脂质体两性霉素B。米卡芬净组中的202个人和脂质体两性霉素B组中的190个人被包括在每方案分析中。在接受米卡芬净治疗的181名患者(89.6%)和使用脂质体两性霉素B治疗的170名(89.5%)患者中观察到治疗成功。基线时通过嗜中性白血球减少症分层后,比例的差异为0.7%(95%CI -5.3至6.7)。疗效与念珠菌属和感染的主要部位,中性粒细胞减少状态,APACHE II评分以及在研究过程中是否拔除导管无关。米卡芬净治疗相关的不良事件(包括严重或导致治疗中断的不良事件)比脂质体两性霉素B少。两性霉素B作为念珠菌血症和浸润性念珠菌病的一线治疗。

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