FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2965352997> ?p ?o ?g. }

• W2965352997 endingPage "677" @default.
• W2965352997 startingPage "675" @default.
• W2965352997 abstract "To the Editor, Histamine and cysteinyl leukotrienes (CysLTs) are potent inflammatory mediators involved in both seasonal allergic rhinoconjunctivitis (SARC) and asthma.1, 2 A combination therapy against both these agents may provide additive benefit, as demonstrated both in vitro 3 and in vivo.4-6 We compared the efficacy and safety of concomitant therapy with bilastine, a second-generation H1 anti-histamine7 and montelukast vs each agent alone in patient with SARC and asthma. We hypothesized that bilastine plus montelukast is superior to bilastine monotherapy in reducing SARC symptoms after 4 weeks and in improving asthma quality of life over a longer time period. Adult patients with SARC and mild-to-moderate asthma partially controlled8 by beclomethasone dipropionate or equivalent ≤500 μg/d (alone or in combination with long-term β2-adrenergic bronchodilators) were enrolled. Patients had a postbronchodilator FEV1 > 70% of the predicted, a skin prick test positive to at least one seasonal allergen tested at enrolment or previously reported, and a nasal/ocular Total Symptom Score (TSS) ≥3.9 Exclusion criteria are reported in the online supplementary. The study (EUDRA-CT number:2015-004806-40) was conducted in 50 centres across 6 European countries during the relevant regional pollen season for grasses, trees and weeds, with a double-blind, double-dummy, randomized, active-controlled and parallel-group design (Figure 1). It consisted in a 1-week screening period followed by 12 weeks of treatment. During the study, patients quantified SARC symptoms by TSS, Daytime Nasal Symptom Score (DNSS) and Daytime non-Nasal Symptom Score (DNNS); use of rescue medications and occurrence of adverse events were noted. During screening, patients’ medical history, vital signs, spirometry results and asthma quality of life questionnaire (AQLQ) scores were obtained. AQLQ was re-assessed after 4 and 12 weeks of treatment; ECG variables, blood and urine samples were re-obtained at the end of treatments for safety purposes. Enrolled patients were randomly treated once daily with bilastine 20 mg plus montelukast 10 mg, or bilastine 20 mg plus placebo or montelukast 10 mg plus placebo (Figure 1). Naphazoline nasal spray eye drops and salbutamol inhaler were rescue medications for SARC and acute asthma symptoms. Patients’ compliance with treatments was calculated. The primary endpoint was changes in baseline TSS values following 4 weeks of treatment.10 Secondary endpoints were changes in baseline TSS values obtained after 1, 2 and 3 weeks of treatment; changes in baseline DNSS and DNNSS values obtained after 1, 2, 3 and 4 weeks of treatments; changes in baseline AQLQ score obtained after 4 and 12 weeks of treatment. Analyses were performed on the intention-to-treat (ITT) population, ie randomized patients who had received at least one treatment tablet, had a baseline assessment and at least one assessment of primary efficacy variable after the baseline visit. A sensitivity analysis was also performed on the per-protocol (PP) population, ie patients in the ITT population having completed the study without any major protocol violation. The effect of each treatment on primary and secondary endpoints, as well as on use of rescue medications for SARC and asthma was compared by analysis of covariance. A P value <.05 was considered as significant. Additional details on the methods are in the online supplementary. From April to October 2016, we enrolled 454 patients, 419 of whom (299 females, mean age 35.2 ± 0.2) were randomized to treatment (ITT population). Of these 419 patients, 387 completed the study without protocol violations (PP population, Figure S1). Reasons of patients exclusion are reported in the Figure S1 (data supplement). Most patients had polisensitization to pollens of grasses, trees and weeds. At inclusion, patients’ demographics, FEV1, TSS, AQLQ, DNSS and DNNSS were similar in each treatment arm (Table S1). All treatments significantly (P < .001) reduced baseline TSS values over 4 weeks (Figure 2). Overall, the mean ± SD TSS reduction was −3.2 ± 3.7, with no significant differences among treatments. Mean TSS value observed 1 and 2 weeks after bilastine was significantly (P < .05) lower than after montelukast. (Figure 2). Mean TSS values decreased similarly with all treatments after 3 weeks (Figure 2). However, bilastine reduced baseline TSS more than montelukast after 1 and 2 weeks of treatment (P always <.05). Similar findings were observed for DNSS and DNNSS (data not shown). Mean AQLQ increased similarly with all treatments after 4 and 12 weeks. The use of rescue medications for SARC and/or asthma did not differ among treatments, as was patients’ compliance with treatments (98.3% overall). Drug-related incidence of adverse events was similar among the treatment groups (4.3% overall). No clinically significant changes in any laboratory tests, ECGs or vital signs were noted. We compared for the first time the efficacy and safety of concomitant administration of bilastine with montelukast vs respective monotherapies in a large population of patients with SARC and asthma. Contrary to our original hypothesis, concomitant administration of bilastine with montelukast was effective as either agent alone in the treatment of SARC symptoms. The reason(s) for not showing any additive effects of bilastine plus montelukast compared with each agent alone could be likely related to the overall mild intensity of SARC symptoms at baseline that might have reduced the room for improvement thus limiting the probability to detect differences between treatments. The absolute extent of the effect of treatments on symptoms or on the use of rescue medications is impossible to gauge as a placebo arm was not included. Noteworthy, the improvement in TSS values observed in our study is similar to that obtained after 2 weeks of placebo treatment by Bachert et al.9 Although the underlying cause is unclear, the large placebo effect observed by Bachert et al9 is not uncommon as observed in other studies with SARC patients.11 Bilastine alone improved SARC symptoms more than montelukast in the first 2 weeks of treatment. This finding is consisted with a more rapid effect of bilastine than montelukast, which may be of relevance for patients who need intermittent treatment to alleviate SARC symptoms. The absolute extent of the effect of these treatments on symptomatology or the use of rescue medication when treating SARC and concomitant asthma are impossible to gauge from this study because a group of patients treated entirely with placebo was not included. Moreover, since changes in lung function were not monitored, it is difficult to gauge how far this improvement reflected possible effects of study treatments on bronchoconstriction and/or lower airways inflammation or how far they reflected a true placebo effect. Previous reports suggest that an improvement in SARC can also improve asthma control.12 Thus, due to its beneficial effects on SARC symptoms, our results suggest that bilastine, when added to inhaled corticosteroids alone or in combination with long-term β2-adrenergic bronchodilators, could improve disease control in mild-to-moderate asthma patients. In conclusion, treatment with bilastine plus montelukast over 4 weeks does not consistently produce further improvements in SARC symptoms and AQLQ beyond those provided by either agent alone. Thus, there is no benefit of using bilastine plus montelukast to provide relief of SARC symptoms in partially controlled, mild-to-moderate asthma patients. We thank Prof. Chris Corrigan for his helpful advice. The SKY study was sponsored by Menarini International Operations Luxemburg SA (MIOL). Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
• W2965352997 created "2019-08-13" @default.
• W2965352997 creator A5014039023 @default.
• W2965352997 creator A5045112331 @default.
• W2965352997 creator A5065764475 @default.
• W2965352997 creator A5082606231 @default.
• W2965352997 date "2019-10-24" @default.
• W2965352997 modified "2023-10-14" @default.
• W2965352997 title "Concomitant bilastine and montelukast as additive therapy for seasonal allergic rhinoconjunctivits and mild‐to‐moderate asthma. The SKY study" @default.
• W2965352997 cites W1973319846 @default.
• W2965352997 cites W1995104897 @default.
• W2965352997 cites W2019443108 @default.
• W2965352997 cites W2032148343 @default.
• W2965352997 cites W2076928017 @default.
• W2965352997 cites W2104985484 @default.
• W2965352997 cites W2121872020 @default.
• W2965352997 cites W2150536351 @default.
• W2965352997 cites W2160918196 @default.
• W2965352997 cites W2167950725 @default.
• W2965352997 doi "https://doi.org/10.1111/all.14007" @default.
• W2965352997 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7078869" @default.
• W2965352997 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31376160" @default.
• W2965352997 hasPublicationYear "2019" @default.
• W2965352997 type Work @default.
• W2965352997 sameAs 2965352997 @default.
• W2965352997 citedByCount "9" @default.
• W2965352997 countsByYear W29653529972020 @default.
• W2965352997 countsByYear W29653529972021 @default.
• W2965352997 countsByYear W29653529972022 @default.
• W2965352997 countsByYear W29653529972023 @default.
• W2965352997 crossrefType "journal-article" @default.
• W2965352997 hasAuthorship W2965352997A5014039023 @default.
• W2965352997 hasAuthorship W2965352997A5045112331 @default.
• W2965352997 hasAuthorship W2965352997A5065764475 @default.
• W2965352997 hasAuthorship W2965352997A5082606231 @default.
• W2965352997 hasBestOaLocation W29653529971 @default.
• W2965352997 hasConcept C126322002 @default.
• W2965352997 hasConcept C203014093 @default.
• W2965352997 hasConcept C207480886 @default.
• W2965352997 hasConcept C2776042228 @default.
• W2965352997 hasConcept C2776322731 @default.
• W2965352997 hasConcept C2779384505 @default.
• W2965352997 hasConcept C71924100 @default.
• W2965352997 hasConceptScore W2965352997C126322002 @default.
• W2965352997 hasConceptScore W2965352997C203014093 @default.
• W2965352997 hasConceptScore W2965352997C207480886 @default.
• W2965352997 hasConceptScore W2965352997C2776042228 @default.
• W2965352997 hasConceptScore W2965352997C2776322731 @default.
• W2965352997 hasConceptScore W2965352997C2779384505 @default.
• W2965352997 hasConceptScore W2965352997C71924100 @default.
• W2965352997 hasIssue "3" @default.
• W2965352997 hasLocation W29653529971 @default.
• W2965352997 hasLocation W29653529972 @default.
• W2965352997 hasLocation W29653529973 @default.
• W2965352997 hasOpenAccess W2965352997 @default.
• W2965352997 hasPrimaryLocation W29653529971 @default.
• W2965352997 hasRelatedWork W1982337671 @default.
• W2965352997 hasRelatedWork W2043240135 @default.
• W2965352997 hasRelatedWork W2106653639 @default.
• W2965352997 hasRelatedWork W2126856804 @default.
• W2965352997 hasRelatedWork W2155991787 @default.
• W2965352997 hasRelatedWork W2553378367 @default.
• W2965352997 hasRelatedWork W2619141725 @default.
• W2965352997 hasRelatedWork W2894848803 @default.
• W2965352997 hasRelatedWork W4221070417 @default.
• W2965352997 hasRelatedWork W4322724676 @default.
• W2965352997 hasVolume "75" @default.
• W2965352997 isParatext "false" @default.
• W2965352997 isRetracted "false" @default.
• W2965352997 magId "2965352997" @default.
• W2965352997 workType "article" @default.