Lung | 2021
Coming Soon: The First-Ever Drug(s) for Refractory Chronic Cough
Abstract
Cough is the most common complaint for which patients in the United States seek medical attention [1]. Chronic cough is widely defined as a cough of greater than 8 weeks’ duration, and is often due to a treatable underlying cause, such as upper airway cough syndrome (postnasal drip syndrome; rhinitis); asthma and non-asthmatic eosinophilic bronchitis; and gastroesophageal reflux disease (GERD) [2]. Chronic cough that does not respond to appropriate therapeutic trials aimed at underlying etiologies is termed refractory chronic cough (RCC). An additional term, unexplained chronic cough (UCC), has recently emerged to describe a chronic cough for which no underlying etiology is identified after adequate investigation [3]. The term Cough Hypersensitivity Syndrome proposes a mechanistic basis for chronic refractory or unexplained cough, that being vagal nerve hypersensitivity resulting in cough reflex hypersensitivity [4]. Appropriate treatment of an established underlying cause of chronic cough will usually be successful. Unfortunately, a significant percentage of patients will prove to have chronic cough refractory to all therapeutic interventions (RCC or UCC). For this subgroup of patients, few if any effective and well-tolerated therapeutic options exist. A minority of patients will obtain benefit from low-dose morphine [5], amitriptyline [6], gabapentin [7], or pregabalin and speechlanguage therapy [8]. Often, antitussive effect is achieved at the expense of intolerable side effects such as sedation. Thus, there exists a great unmet need for safe, effective, nonnarcotic, non-sedating agents for the treatment of refractory chronic cough. The last antitussive medication approved by the United States Food and Drug Administration (FDA) was benzonatate, in 1958 [9]. The widely used non-prescription antitussive, dextromethorphan, was approved in 1954 [9]. To date, there has not been a drug approved in the United States for the indication of chronic cough. Thankfully, the last decade has witnessed significant scientific achievement in understanding the mechanisms of chronic cough, which has led to multiple clinical drug development programs exploring potential novel antitussive agents. The most advanced of these efforts is in the area of purinergic receptors, of which the P2X class functions as ligand-gated ion channels that are responsive to ATP [10]. In the airways, purines including ATP can trigger reflexes through the activation of vagal sensory nerves, and ATP may sensitize airway sensory nerves to tussive stimuli [10]. The P2X3 homotrimer and P2X2/3 heterotrimer have been implicated as most relevant in cough induction, with the latter also being essential to the sensation of taste [10]. The first-in-class P2X3 receptor antagonist, gefapixant, demonstrated significant antitussive effect in phase 2 trials, but at the expense of diminution of taste sensation in a significant subgroup of subjects [11]. Two phase 3 trials of gefapixant have been completed recently, and published data are awaited. Three additional drug development programs are ongoing, evaluating whether more selective P2X3 receptor antagonists may provide similar or better antitussive efficacy with less taste effect [10]. In this issue of LUNG, Morice and colleagues [12] provide a detailed description of a group of 253 subjects with RCC or UCC who had participated in a phase 2 clinical trial of gefapixant [11]. Enrollment criteria included duration of cough of at least one year; a subjective baseline cough severity score of ≥ 40 mm on a 100-mm visual analog scale (VAS) with 100 mm indicating most severe cough; and nonsmoking status (either never smoker or cessation > 6 months prior to enrollment). Demographic characteristics of the subject population were quite consistent with those previously reported of patients seeking evaluation at specialty cough centers worldwide: predominance of women and lifetime non-smokers; mean age of patients 55 years, and most common age of presentation 60–69 years [13]. Although the very long median duration of cough (11 years) and high objectively measured median awake * Peter V. Dicpinigaitis [email protected]