Rapid onset of action and reduced nasal hyperreactivity: new targets in allergic rhinitis management

The aim of AR management is to gain control of the disease. As for asthma, the control concept is important for the rhinitis management landscape [18, 19]. Unfortunately, many patients with AR continue to live with uncontrolled disease [20]. In order to understand how AR control may be achieved in real-life, it is necessary to understand the complexity of the AR management landscape, and to know what AR patients really expect from their treatment.

Complexity of the AR landscape manifests in many ways. Firstly, a disparity exists in perspectives between physicians and AR patients, to the effect that AR is under-diagnosed, under-estimated and under-treated; the majority of physicians do not use adequate AR treatment [21]. Secondly, AR patient behaviour, as it pertains to their AR management, can be disorganized and inconsistent [22‐24]. Up to two-thirds of AR patients simply forget to take their medication [24]. Thirdly, there is a reticence to seek professional medical advice, and a tendency to do so only when symptoms become ‘intolerable^’ [22] or if symptoms persist after trying several over the counter (OTC) options [23]. An internet and telephone survey conducted with 2966 randomly selected adults with allergies showed that 52.6% of respondents had not seen a medical professional in the past year for their rhinitis symptoms, with some 30.2% preferring non-prescription medication because it did not involve a doctor visit [22]. Fourthly, AR patients glean a lot of information about their disease from the internet, and there is a high degree of self-management, a consequence of the large choice of OTC AR medications available [25‐28]. It is therefore, crucial that AR care pathways should consider pharmacists [29]. The vast majority of AR patients use 2 or more AR medications in an effort to achieve faster and more effective relief from their nasal and ocular symptoms [30] (a practice which is not endorsed by the evidence) [31‐33], with many patients calling for more efficacious OTC AR medications to better manage their AR symptoms [23]. Finally, most patients suffer from several episodes of short-term AR symptoms [30], and so rarely take their medication continuously for 14 days, as envisaged in the vast majority of seasonal AR randomized controlled trials (RCTs). Indeed, there is little evidence supporting the daily use of rhinitis treatment. For example, a recent study of pollen-AR in children found that on-demand fluticasone propionate (FP) treatment was at least as effective as a regular treatment at a lower dose [34].

To gain a better understanding of what patients want from their AR treatment, we should simply ask them. A survey conducted in Belgium showed that patients have high expectations from their AR treatment and have preferences in terms of AR medication delivery and approach [35]. 40% of these patients expected their AR to be cured by pharmacological intervention, with 30% preferring intranasal sprays (vs 24% for oral therapy), and 31% of respondents preferring a combination treatment with a step down approach. When asked, AR patients listed good 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 [23]. A different type of patient survey, called a discrete choice experiment quantified what patients want from their AR treatment, using a willingness to pay metric, and confirmed the results of the AR patient surveys [23, 35, 36]. The findings showed that patients want more complete symptom relief from their AR treatment and are willing to pay £43.81 (approx. €55) to achieve that (vs mild relief). Rapidity of response was also very important to AR patients, both in terms of time to maximum response and time to first response (i.e. onset). Patients were willing to pay £0.98 (approx. €1.10) for each hour faster to onset and £0.62 (approx. €0.70) for each day faster to maximum complete relief from AR symptoms. These surveys highlight the importance of involving patients in AR management and tailoring the AR treatment to the individual. By listening to AR patients we can empower them to establish their own treatment goals, manage treatment expectations, and incorporate treatment preferences into their AR treatment regimen. And this has benefits for the physician too; up to 96% of physicians consider that taking AR patients’ opinions into account increases therapeutic adherence [37]. Patient participation in the design of the treatment strategy is one of the 4 key pillars of precision medicine and believed to be a key success factor of treatment [17].

MACVIA-ARIA (Contre les Maladies Chroniques pour un Vieillissment Actif-Allergic Rhinitis and its Impact on Asthma) have recommended a patient-centered, mobile-health and clinical decision support system (CDSS) approach to achieve AR control in real life, linking all stakeholders in AR management (i.e. patients, healthcare providers (HCPs), regulators and guideline producers/implementers) [38]. This has been done by establishing a common language of AR control, a simple visual analogue scale (VAS) [18, 19, 39], and incorporating this VAS into free apps for patients [7, 40‐42] and HCPs, as well as into an AR CDSS [18]. A VAS score cut-off of 5/10 cm is used to assess control and guide treatment decisions [18]. Allergy Diary is the app for patients. It is part of the MASK initiative (Mobile Airways Sentinel networK), and is included in the B3 action plan of the European Innovation Partnership on Active and Health Aging [43]. Data obtained from the Allergy Diary have enabled us for the first time to see how patients really treat their AR in real life and to recognize how this vastly differs from the RCT environment. The Allergy Diary data showed that In real-life patients (1) are poorly compliant with their AR treatment; (2) rapidly switch from one AR treatment to another if the desired response is not achieved; (3) often use multiple AR therapies; (4) fail to achieve sustained AR control on an intranasal corticosteroid (INS) monotherapy or anti-histamine + INS therapy; (5) achieve good control on more effective therapies, like MP-AzeFlu (Dymista^®, Mylan Inc, USA); but (5) often switch back to less effective therapies when AR is well-controlled. Figure 1 shows Allergy Diary data from one typical AR user,inputted between Aug and Dec 2015. As can be seen, treatment is neither consistent nor consecutive. This user started with a multiple treatment regimen (INS + anti-histamine), switching to MP-AzeFlu (or MP-AzeFlu + anti-histmanine) to achieve MACVIA-ARIA defined disease control (i.e. VAS score < 5/10 cm). AR control was lost upon swiching to INS monotherapy, and regained once again on MP-AzeFlu (Fig. 1).

Better AR control may be achieved by listening to patients, taking account of how they actually manage their AR and providing what they want. Based on the evidence presented here, patients want an AR therapy, which provides complete and long-lasting symptom relief (i.e. no breakthrouh symptoms) and which has a rapid onset of action.

MP-AzeFlu, is a relatively new addition to the AR treatment armamentarium, comprising intranasal azelastine (AZE) and FP in a novel formulation delivered in a single device [44]. Its onset of action has recently been investigated in an allergen exposure chamber and compared with an AR treatment regimen frequently used by AR patients in real life (i.e. anti-histamine + INS), in a single-centre, double-blind, double-dummy 3-period cross-over RCT [45]. AR symptoms were induced in asymptomatic patients (n = 82) in response to ragweed pollen challenge in the Ontario environmental exposure chamber. Patients then received a single dose of MP-AzeFlu (137/50 μg, 1 spray/nostril); intranasal FP (50 μg, 1 spray/nostril) plus oral loratadine (LOR; 10 mg) or placebo, and were monitored for 4 h. Symptoms were assessed at 5, 10, 15, 30, 60, 90, 120, 150, 180, 210 and 240 min after dosing. The primary outcome was onset of action measured by total nasal symptom score (TNSS). The TNSS comprises individual scores for nasal congestion, itching, rhinorrhoea and sneezing, with each of these scored from 0 (none) to 3 (severe), giving a maximum score of 12. Clinical relevance was assessed both from the individual and population perspective, using Kaplan–meier curves for time to response and minimally important clinical difference (MICD), respectively. A clinically relevant response was defined as at least 50% change from baseline in TNSS. MICD for TNSS was calculated using a sample size adjusted pooled estimate of baseline standard deviations. A difference of 0.47 points was defined as a small effect and 1.17 points defined as a medium effect [45].

As can be seen from Fig. 2, the onset of action for MP-AzeFlu was 5 min compared to 150 min for FP + oral LOR, a difference of almost 2.5 h [45]. MP-AzeFlu also provided significantly (p = 0.005) greater nasal symptom relief than FP + LOR, which did not differ from placebo during the 4 h study period (p = 0.182). Furthermore, MP-AzeFlu achieved the 1.17 medium MICD in rTNSS at 15 min, compared to both placebo and to FP + LOR. By contrast, patients treated with FP + LOR experienced this difference vs placebo at 210 min, more than 3 h later. When assessing clinical relevance in terms of 50% reduction from baseline in TNSS, 71.3% of patients treated with MP-AzeFlu achieved this clinically relevant response, and did so significantly faster than those treated with FP + LOR (p < 0.001) or placebo (p = 0.002), approximately 2.5 h faster [45]. MP-AzeFlu’s rapid onset of action and rapid clinically relevant effect should improve AR control, with this profile fitting well with prn use of AR medications and rapid treatment switching observed in real life.

As many as 36.5% of patients currently on an AR treatment continue to experience poorly controlled AR (i.e. VAS score ≥ 5), with this number remaining essentially the same irrespective of the type of pharmacological treatment used, be it INS (38.5%), oral anti-histamine (34.9%) or multiple therapies (35.9%) [20]. This situation is familiar to HCPs, who consider that 58% of their AR patients have either uncontrolled or poorly controlled disease [39]. Lack of AR control is influenced by 4 factors, namely (1) diagnosis-related (e.g. incorrect diagnosis, presence of co-morbidity); (2) treatment-related (e.g. insufficient efficacy or lack of targeted symptom relief); (3) patient-related (e.g. poor adherence); and (iv) disease-related (e.g. treatment resistant phenotypes) [19]. Using an AR treatment with a rapid onset of action and rapid clinically relevant effect is one way to improve AR control, presumably by addressing patient-related factors; improving adherence to therapy, or perhaps being more forgiving of poor adherence. Another way to achieve better AR control is to address disease-related factors by targeting an alternative disease pathway. Nasal hyperreactivity (NHR) is an important clinical feature of AR, which is present in up to two-thirds of AR patients [46], and may be responsible for breakthrough symptoms frequently reported by AR patients and dissatisfaction with treatment. NHR is defined as an increased sensitivity of the nasal mucosa to environmental, non-specific stimuli (e.g. temperature/humidity changes, smoke, strong odours, exercise and emotional stress), leading to nasal symptoms [47, 48]. The effect of MP-AzeFlu on cold dry air (CDA)-induced-NHR was assessed in a 4-week double-blind, placebo-controlled trial in 28 AR patients with a house dust mite sensitivity [49].

Patients with moderate/severe persistent AR and NHR (i.e. reduced peak nasal inspiratory flow (PNIF) > 20% upon CDA provocation) were randomized 2:1 to receive either MP-AzeFlu (1 spray/nostril bd) or placebo. The effect of MP-AzeFlu on NHR was assessed by PNIF decrease in response to CDA, as well as on the severity of nasal symptoms, measured at baseline and after 7 and 28 days of treatment [49]. Nasal symptom severity was assessed in two ways, by total of 5 symptom scores (T5SS; comprising scores for congestion, nasal itching, rhinorrhoea, sneezing and ocular itching—max score = 15) and by VAS (0–10 cm). AR control was assessed using the AR control test. To investigate the mechanism(s) behind any observed reduction in NHR, the effect of MP-AzeFlu on substance P and β-hexosaminidase concentrations in human nasal secretions was assessed. MP-AzeFlu’s effect on mucosal barrier integrity, mast cell degranulation and airway inflammation in a mouse model of house dust mite-induced NHR, as well as its effect on murine sensory neurons from trigeminal ganglia was also investigated [49].

The results showed that MP-AzeFlu significantly (p < 0.0001) reduced NHR (Fig. 3a), with a correlating and significant reduction in nasal symptom severity observed (Fig. 3b, c) [49]. Nasal symptoms were reduced following 28 day’s treatment with MP-AzeFlu by approximately 80% when assessed by T5SS and by 90% when assessed by VAS. Patients treated with MP-AzeFlu for 28 days also experienced significantly (p = 0.035) better AR control compared to placebo. An investigation of the underlying pathophysiology of this NHR reduction revealed that MP-AzeFlu significantly reduced Substance P (p = 0.026) and β-hexosaminidase concentrations (p = 0.036) in nasal secretions, both at Day 7 and Day 28, which was not found in the placebo group [49]. In vitro, AZE + FP inhibited human mast cell degranulation (better than FP and to the same extent as AZE) and decreased murine epithelial permeability (better than AZE and to the same extent as FP). MP-AzeFlu also totally abrogated eosinophils (and neutrophils) in bronchoalveolar lavage fluid in the same murine model of HDM-induced allergic airway inflammation, compared to both AZE and FP, demonstrating a synergistic effect on airway inflammation [49]. Furthermore, only AZE + FP (and not AZE or FP alone) evoked a rapid intracellular Ca²⁺ increase, with repeated applications of AZE + FP resulting in desensitization of sensory neurons expressing the transient receptor potential (TRP) A1 and V1 channels [49]. Activation of these neuronal channels is responsible for the development of idiopathic rhinitis and non-allergic hyperreactivity [50, 51]. MP-AzeFlu’s specific targeting of NHR represents a novel pathway in the pathophysiology of AR, helping to explain the clinical superiority and over-additive effects of MP-AzeFlu seen in clinical practice [52, 53], and providing patients with the complete symptom relief and lack of breakthrough symptoms that they want.