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伊曲康唑治疗毛霉病:一项单臂开放标签试验和病例对照分析。

Isavuconazole treatment for mucormycosis: a single-arm open-label trial and case-control analysis.

机构信息

Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA, USA.

University of Texas Medical School at Houston and Memorial Hermann Texas Medical Center, University of Texas, Houston, TX, USA.

出版信息

Lancet Infect Dis. 2016 Jul;16(7):828-837. doi: 10.1016/S1473-3099(16)00071-2. Epub 2016 Mar 9.

Abstract

BACKGROUND

Mucormycosis is an uncommon invasive fungal disease with high mortality and few treatment options. Isavuconazole is a triazole active in vitro and in animal models against moulds of the order Mucorales. We assessed the efficacy and safety of isavuconazole for treatment of mucormycosis and compared its efficacy with amphotericin B in a matched case-control analysis.

METHODS

In a single-arm open-label trial (VITAL study), adult patients (≥18 years) with invasive fungal disease caused by rare fungi, including mucormycosis, were recruited from 34 centres worldwide. Patients were given isavuconazole 200 mg (as its intravenous or oral water-soluble prodrug, isavuconazonium sulfate) three times daily for six doses, followed by 200 mg/day until invasive fungal disease resolution, failure, or for 180 days or more. The primary endpoint was independent data review committee-determined overall response-ie, complete or partial response (treatment success) or stable or progressive disease (treatment failure)-according to prespecified criteria. Mucormycosis cases treated with isavuconazole as primary treatment were matched with controls from the FungiScope Registry, recruited from 17 centres worldwide, who received primary amphotericin B-based treatment, and were analysed for day-42 all-cause mortality. VITAL is registered with ClinicalTrials.gov, number NCT00634049. FungiScope is registered with ClinicalTrials.gov, number NCT01731353.

FINDINGS

Within the VITAL study, from April 22, 2008, to June 21, 2013, 37 patients with mucormycosis received isavuconazole for a median of 84 days (IQR 19-179, range 2-882). By day 42, four patients (11%) had a partial response, 16 (43%) had stable invasive fungal disease, one (3%) had invasive fungal disease progression, three (8%) had missing assessments, and 13 (35%) had died. 35 patients (95%) had adverse events (28 [76%] serious). Day-42 crude all-cause mortality in seven (33%) of 21 primary-treatment isavuconazole cases was similar to 13 (39%) of 33 amphotericin B-treated matched controls (weighted all-cause mortality: 33% vs 41%; p=0·595).

INTERPRETATION

Isavuconazole showed activity against mucormycosis with efficacy similar to amphotericin B. Isavuconazole can be used for treatment of mucormycosis and is well tolerated.

FUNDING

Astellas Pharma Global Development, Basilea Pharmaceutica International.

摘要

背景

毛霉菌病是一种罕见的侵袭性真菌感染,死亡率高,治疗选择有限。伊曲康唑是一种三唑类药物,在体外和动物模型中对毛霉菌目霉菌具有活性。我们评估了伊曲康唑治疗毛霉菌病的疗效和安全性,并在匹配的病例对照分析中比较了其与两性霉素 B 的疗效。

方法

在一项单臂开放标签试验(VITAL 研究)中,来自全球 34 个中心的成年患者(≥18 岁)患有罕见真菌引起的侵袭性真菌感染,包括毛霉菌病。患者接受伊曲康唑 200mg(作为其静脉或口服水溶性前药伊曲康唑硫酸),每日 3 次,共 6 剂,然后每日 200mg,直至侵袭性真菌感染得到解决、失败或治疗超过 180 天。主要终点是独立数据审查委员会确定的总体反应,即完全或部分反应(治疗成功)或稳定或进展性疾病(治疗失败),根据预设标准。用伊曲康唑作为主要治疗的毛霉菌病病例与来自全球 17 个中心的 FungiScope 登记处招募的对照病例相匹配,这些对照病例接受了基于两性霉素 B 的主要治疗,并分析了第 42 天的全因死亡率。VITAL 在 ClinicalTrials.gov 上注册,编号为 NCT00634049。FungiScope 在 ClinicalTrials.gov 上注册,编号为 NCT01731353。

结果

在 VITAL 研究中,从 2008 年 4 月 22 日至 2013 年 6 月 21 日,37 例毛霉菌病患者接受伊曲康唑治疗,中位治疗时间为 84 天(IQR 19-179,范围 2-882)。第 42 天,4 名患者(11%)有部分反应,16 名患者(43%)有稳定的侵袭性真菌感染,1 名患者(3%)有侵袭性真菌感染进展,3 名患者(8%)有缺失评估,13 名患者(35%)死亡。35 名患者(95%)发生不良事件(28 [76%]严重)。21 例主要治疗伊曲康唑病例中,7 例(33%)在第 42 天的粗全因死亡率与 33 例接受两性霉素 B 治疗的匹配对照病例(加权全因死亡率:33% vs 41%;p=0·595)相似。

解释

伊曲康唑对毛霉菌病具有活性,疗效与两性霉素 B 相似。伊曲康唑可用于治疗毛霉菌病,且耐受性良好。

资金来源

安斯泰来制药全球开发公司、百时美施贵宝国际有限公司。

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