Bachert C, Bousquet J, Hellings P
1Ghent University Hospital, Ghent, Belgium.
2Upper Airways Research Laboratory, University of Ghent, Ghent, Belgium.
Clin Transl Allergy. 2018 Jun 25;8:25. doi: 10.1186/s13601-018-0210-2. eCollection 2018.
This article summarizes a EUFOREA symposium, presented during the European Rhinology Research Forum in Brussels (9-10 November 2017; https://www.rhinologyresearch.eu/) which focused on novel pathways and therapeutic approaches in allergic rhinitis (AR).
AR remains under-diagnosed, under-estimated and under-treated. A key component in understanding the AR landscape has been the realization of a significant mismatch between how physicians instruct AR patients to manage their disease and what AR patients actually do in real life. Data from the (developed by MACVIA ARIA) showed that AR patients take their medication prn, rapidly switch treatments, often experience poor control, use multiple therapies and stop treatment when symptoms are controlled. Better control of AR may be achievable by using an AR treatment which has a rapid onset of action and which effectively targets breakthrough symptoms. Indeed, AR patients report complete symptom relief, lack of breakthrough symptoms, rapid onset of action, safety and use on an 'as needed' basis as key targets for new nasal sprays. MP-AzeFlu comprises intranasal azelastine and fluticasone propionate (FP) in a novel formulation delivered in a single device. It is the first AR treatment to break the 5 min onset of action threshold and provides clinically relevant symptom relief in 15 min, much faster than that noted for FP + oral loratadine. MP-AzeFlu also significantly reduces nasal hyperresponsiveness (NHR) which may be responsible for the breakthrough symptoms frequently reported by AR patients. Mechanisms underlying MP-AzeFlu's effect include inhibition of mast cell degranulation, stabilization of the mucosal barrier, synergistic inhibition of inflammatory cell recruitment and a unique desensitization of sensory neurons expressing the transient receptor potential A1 and V1 channels.
With the most rapid onset of action and onset of clinically-relevant effect of any AR medication currently available, and proven efficacy in the treatment of NHR, MP-AzeFlu is an AR treatment which provides what patients want, and fits how patients manage their AR in real life.
本文总结了在布鲁塞尔举行的欧洲鼻科学研究论坛(2017年11月9 - 10日;https://www.rhinologyresearch.eu/)期间举办的一场欧盟鼻科学与过敏研究协会(EUFOREA)研讨会,该研讨会聚焦于变应性鼻炎(AR)的新途径和治疗方法。
AR仍然存在诊断不足、重视不够和治疗不足的问题。理解AR现状的一个关键因素是认识到医生指导AR患者管理疾病的方式与AR患者在现实生活中的实际做法之间存在显著差异。(由MACVIA ARIA开发的)数据显示,AR患者按需服药,迅速更换治疗方法,经常控制不佳,使用多种疗法,并且在症状得到控制时就停止治疗。通过使用起效迅速且能有效针对突发症状的AR治疗方法,可能实现对AR更好的控制。事实上,AR患者报告称,完全缓解症状、无突发症状、起效迅速、安全以及按需使用是新型鼻喷雾剂的关键目标。MP - 氮卓斯汀氟替卡松(MP - AzeFlu)由鼻用氮卓斯汀和丙酸氟替卡松(FP)组成,采用新颖配方,通过单一装置给药。它是首个突破5分钟起效阈值的AR治疗药物,15分钟内即可提供临床相关的症状缓解,比FP加口服氯雷他定快得多。MP - AzeFlu还能显著降低鼻高反应性(NHR),而NHR可能是AR患者经常报告的突发症状的原因。MP - AzeFlu作用的潜在机制包括抑制肥大细胞脱颗粒、稳定黏膜屏障、协同抑制炎症细胞募集以及对表达瞬时受体电位A1和V1通道的感觉神经元进行独特的脱敏作用。
MP - AzeFlu是目前所有AR药物中起效最快且产生临床相关效果最快的,并且在治疗NHR方面已证实有效,它满足了患者的需求,也符合患者在现实生活中管理AR的方式。