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首页> 外文期刊>Drug Design, Development and Therapy >The Use of Amikacin Liposome Inhalation Suspension (Arikayce) in the Treatment of Refractory Nontuberculous Mycobacterial Lung Disease in Adults
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The Use of Amikacin Liposome Inhalation Suspension (Arikayce) in the Treatment of Refractory Nontuberculous Mycobacterial Lung Disease in Adults

机译:使用Amikacin脂质体吸入悬浮液(ARikayce)在成人中治疗难治性无泛的分枝杆菌病

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Nontuberculous mycobacteria (NTM) can cause and perpetuate chronic inflammation and lung infection. Despite having the diagnostic criteria, as defined by the American Thoracic Society (ATS) and Infectious Diseases Society of America (IDSA), clinicians find it challenging to diagnose and treat NTM-induced lung disease. Inhaled antibiotics are suitable for patients with lung infection caused by Pseudomonas aeruginosa and other organisms, but until recently, their utility in NTM-induced infection was not established. The most common NTM pathogens identified are the slow-growing Mycobacterium avium complex (MAC) and the rapid-growing M. abscessus complex (MABSC), both of which include several subspecies. Other less commonly isolated species include M. kansasii, M. simiae , and M. fortuitum . NTM strains are frequently more resistant than what is found in bacterial sputum cultures. Until recently, there was no approved inhaled antibiotic therapy for patients who were culture positive for pulmonary NTM infection. Of late, inhaled amikacin has been under investigation for the treatment of NTM-induced pulmonary infection. The FDA approved Arikayce (amikacin liposome inhalation suspension or ALIS) based on results from the ongoing Phase 3 CONVERT trial. In this study, the use of Arikayce met its primary endpoint of sputum culture conversion by the sixth month of treatment. The addition of Arikayce to guideline-based therapy led to negative sputum cultures for NTM by month 6 in 29% of patients compared to 8.9% of patients treated with guideline-based therapy alone. The effectiveness of Arikayce holds promise. However, due to limited data on Arikayce’s safety, it is currently useful only for a specific population, particularly patients with refractory NTM-induced lung disease. Future trials must verify the target group and endorse the clinical benefits of Arikayce.
机译:Nonuberulous的分枝杆菌(NTM)可以引起慢性炎症和肺部感染。尽管具有诊断标准,但由美国胸部社会(ATS)和传染病学会(IDSA)所定义,临床医生发现诊断和治疗NTM诱导的肺病挑战。吸入的抗生素适用于铜绿假单胞菌和其他生物引起的肺感染患者,但直到最近,他们在NTM诱导的感染中的效用尚未建立。鉴定的最常见的NTM病原体是生长缓慢的分枝杆菌(MAC)和快速生长的M.脓肿复合物(MABSC),其中包括几个亚种。其他较少常见的物种包括M. kansasii,M.Imiae和M. Fortuitum。 NTM菌株通常比细菌痰培养物中的发现更耐受。直到最近,没有批准的吸入抗生素治疗,用于肺结核感染培养的患者。最近,吸入的阿米卡卡蛋白已经进行了治疗NTM诱导的肺部感染。根据正在进行的第3阶段转换试验的结果,FDA批准ARikayce(Amikacin脂质体吸入悬浮液或ALIS)。在这项研究中,ARikayce的使用在第六个月的治疗中满足了痰培养转化率的主要终点。将Arikayce添加到基于指南的疗法导致NTM的阴性痰培养为29%的患者中的60%的患者,而8.9%的患者单独治疗指南治疗。 Arikayce的有效性拥有承诺。然而,由于Arikayce的安全数据有限,目前仅适用于特定人群,特别是难治性NTM诱导的肺病患者。未来的试验必须核实目标群体,并赞同Arikayce的临床福利。

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