Melissa Lipari, Pharm.D., BCACP, is Assistant Professor; Harpreet Benipal, Pharm.D., is a 2013 graduate; and Pramodini Kale-Pradhan, Pharm.D., is Professor, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, and St. John Hospital and Medical Center, Detroit, MI.
Am J Health Syst Pharm. 2013 Dec 1;70(23):2087-95. doi: 10.2146/ajhp130114.
The pharmacology, pharmacokinetics, efficacy, and safety of roflumilast-the first in a new class of agents for managing chronic obstructive pulmonary disease (COPD)-are reviewed.
Roflumilast (Daliresp, Forest Pharmaceuticals) is an oral phosphodiesterase-4 (PDE-4) inhibitor that targets inflammatory cells involved in triggering COPD exacerbations. The only PDE-4 inhibitor approved by the Food and Drug Administration, roflumilast is available in 500-μg tablets to be administered once daily. In six placebo-controlled trials involving nearly 4500 patients with COPD of varying severity, the use of roflumilast was associated with reduced COPD exacerbations and improved lung function, as determined by spirometry, with the greatest benefits observed in patients with severe COPD who had chronic bronchitis and a history of frequent exacerbations; clinical efficacy was demonstrated in patients receiving roflumilast alone as well as those receiving concomitant inhaled long-acting β2-agonist (LABA) therapy. The most common adverse events in clinical trials of roflumilast were diarrhea, nausea, and headache. Weight loss and an increased risk of psychiatric events have also been reported in association with roflumilast use. As roflumilast is rapidly converted to its active metabolite via cytochrome P-450 (CYP) isoenzymes, coadministration with strong CYP inducers is not recommended. Research to better define roflumilast's role in COPD management, including a study to determine whether it confers additive benefits when used in combination with standard inhaled therapies other than LABAs, is ongoing.
Roflumilast is a safe and effective option for controlling COPD exacerbations in a defined subset of patients for whom the available treatment alternatives are very limited.
综述罗氟司特的药理学、药代动力学、疗效和安全性,这是一种用于治疗慢性阻塞性肺疾病(COPD)的新型药物。
罗氟司特(Daliresp,Forest 制药公司)是一种口服磷酸二酯酶-4(PDE-4)抑制剂,针对参与触发 COPD 加重的炎症细胞。作为唯一获得美国食品和药物管理局批准的 PDE-4 抑制剂,罗氟司特以 500μg 片剂形式存在,每日服用一次。在六项涉及近 4500 名不同严重程度 COPD 患者的安慰剂对照试验中,罗氟司特的使用与 COPD 加重减少和肺功能改善相关,通过肺活量测定法确定,在患有慢性支气管炎和频繁加重病史的严重 COPD 患者中观察到最大益处;在单独使用罗氟司特或同时使用吸入长效β2-激动剂(LABA)治疗的患者中都观察到了临床疗效。罗氟司特临床试验中最常见的不良反应是腹泻、恶心和头痛。体重减轻和精神事件风险增加也与罗氟司特的使用有关。由于罗氟司特通过细胞色素 P-450(CYP)同工酶迅速转化为其活性代谢物,因此不建议与强 CYP 诱导剂共同给药。正在进行研究以更好地确定罗氟司特在 COPD 管理中的作用,包括一项研究,以确定当与除 LABA 以外的标准吸入疗法联合使用时,它是否具有附加益处。
对于那些可供选择的治疗方案非常有限的特定 COPD 患者亚组,罗氟司特是一种安全有效的控制 COPD 加重的选择。