a Chair of Respiratory Medicine, Department of Systems Medicine , University of Rome Tor Vergata , Rome , Italy.
b Unit of Pharmacology, Department of Experimental Medicine , Second University of Naples , Naples , Italy.
Expert Opin Drug Discov. 2016 Jul;11(7):733-44. doi: 10.1080/17460441.2016.1184642. Epub 2016 May 21.
Cyclic adenosine monophosphate (cAMP) phosphodiesterase (PDE)4 is an intracellular target that can be exploited to the treat chronic obstructive pulmonary disease (COPD), given that it is expressed in all inflammatory cells implicated in this inflammatory airways disease. At the present time, roflumilast is the only PDE4 inhibitor that has received regulatory approval for use in patients with COPD.
The preclinical, clinical and post-marketing development of roflumilast is described. Furthermore, a critical analysis of the clinical data and positioning of this drug is undertaken in this review Expert opinion: The identification of a subset of COPD patients, namely those suffering from severe airflow obstruction with symptoms of chronic cough and sputum and a history of previous exacerbations, as a specific target for roflumilast with the goal of reducing exacerbations, was entirely casual because the delineation of a 'chronic bronchitis' responder group was clearly a post-hoc finding. However, it was useful to design prospective clinical trials that demonstrated reduced exacerbations in this specific subset of patients towards whom roflumilast therapy is now targeted. In any case, these pivotal trials still do not provide more accurate identification of the type of exacerbation to be treated by roflumilast. The identification of the right biological COPD exacerbation phenotype and/or the right clinical COPD phenotype are the only means that could justify the use of roflumilast as a first line anti-inflammatory therapeutic approach.
环磷酸腺苷(cAMP)磷酸二酯酶(PDE)4 是一种细胞内靶点,可以用于治疗慢性阻塞性肺疾病(COPD),因为它在所有涉及这种炎症性气道疾病的炎症细胞中都有表达。目前,罗氟司特是唯一一种获得监管部门批准用于 COPD 患者的 PDE4 抑制剂。
描述了罗氟司特的临床前、临床和上市后开发情况。此外,在本综述中还对该药的临床数据和定位进行了批判性分析。
将具有严重气流阻塞症状、慢性咳嗽和咳痰以及既往加重史的 COPD 患者亚组确定为罗氟司特的特定靶点,以减少加重,这完全是偶然的,因为“慢性支气管炎”应答组的划定显然是事后发现的。然而,设计前瞻性临床试验以证明在这一特定患者亚组中减少加重是有用的,现在针对这一患者亚组进行罗氟司特治疗。无论如何,这些关键试验仍然不能更准确地确定需要用罗氟司特治疗的加重类型。只有确定正确的生物 COPD 加重表型和/或正确的临床 COPD 表型,才能证明将罗氟司特作为一线抗炎治疗方法的合理性。