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The impact of blood eosinophil count and FeNO on benralizumab effectiveness in clinical practice: An ORBE II subanalysis

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dc.contributor.author García-Moguel, Ismael
dc.contributor.author Martínez-Mesa, Álvaro
dc.contributor.author Andújar-Espinosa, Rubén
dc.contributor.author Díaz-Campos, Rocío
dc.contributor.author Velasco-Garrido, José-Luis
dc.contributor.author Sánchez-Trincado, José-Luis
dc.contributor.author Luzon, Elisa
dc.contributor.author Nuevo, Javier
dc.contributor.author Alconada, Carlos
dc.contributor.author Gutiérrez, Miguel-Ángel
dc.contributor.author Niza, Gabriel
dc.contributor.author Padilla-Galo, Alicia
dc.date.accessioned 2026-03-10T11:49:43Z
dc.date.available 2026-03-10T11:49:43Z
dc.date.issued 2025-02
dc.identifier.citation García-Moguel I, Martínez-Mesa Á, Andújar-Espinosa R, Díaz-Campos R, Velasco-Garrido JL, Sanchez-Trincado JL, et al. The impact of blood eosinophil count and FeNO on benralizumab effectiveness in clinical practice: An ORBE II subanalysis. Respiratory Medicine. febrero de 2025;237:107940. doi:10.1016/j.rmed.2025.107940
dc.identifier.issn 0954-6111
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/25249
dc.description.abstract BACKGROUND: The ORBE II study showed the real-world effectiveness of benralizumab in severe eosinophilic asthma (SEA). This subgroup analysis aimed to characterize patients and outcomes based on baseline blood eosinophil count (BEC) and/or fractional exhaled nitric oxide (FeNO) levels. METHODS: In this analysis of the ORBE II retrospective study, SEA patients receiving benralizumab were categorized into subgroups based on individual or combined BEC/FeNO levels, according to the following thresholds: high BEC (hiBEC): ?300 cells/?L; low BEC (loBEC): <300 cells/?L; high FeNO (hiFeNO): ?50 ppb; low FeNO (loFeNO): <50 ppb. Baseline and up to 1 year of follow-up data are described. RESULTS: Most patients with available data were classified as hiBEC (72.6 %) and 38.3 % as hiFeNO. The distribution according to combined baseline BEC and FeNO levels revealed a heterogeneous patient population. Although common SEA features were shared among subgroups, some distinct characteristics were observed, including elevated allergic asthma prevalence in hiBEC/loFeNO patients, high obesity prevalence and fewer non-smokers in loBEC/loFeNO patients, remarkable severe exacerbation rates in loBEC/hiFeNO patients [5.5 SD (6.0)], and more severe symptoms in the hiBEC/loBEC subgroup. All subgroups showed benefits following benralizumab treatment, with super-responder rates ranging from 68.2 % to 83.3 % and clinical remission rates reaching 70.0 %. Particularly good responses were noted in hiBEC/hiFeNO patients. CONCLUSIONS: This study shows the variability of T2 biomarkers in ORBE II SEA patients, emphasizing the prevalence of high BEC values. While benralizumab benefits were important regardless of BEC, high BEC predicted good outcomes and FeNO had less influence on treatment effectiveness.
dc.language.iso eng
dc.publisher W B SAUNDERS CO LTD
dc.rights Atribución/Reconocimiento 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by/4.0/deed.es
dc.subject.mesh Humans
dc.subject.mesh Eosinophils
dc.subject.mesh Male
dc.subject.mesh Female
dc.subject.mesh Asthma/drug therapy/blood
dc.subject.mesh Antibodies, Monoclonal, Humanized/therapeutic use
dc.subject.mesh Retrospective Studies
dc.subject.mesh Middle Aged
dc.subject.mesh Adult
dc.subject.mesh Anti-Asthmatic Agents/therapeutic use
dc.subject.mesh Leukocyte Count
dc.subject.mesh Treatment Outcome
dc.subject.mesh Nitric Oxide/analysis/metabolism
dc.subject.mesh Fractional Exhaled Nitric Oxide Testing/methods
dc.subject.mesh Aged
dc.title The impact of blood eosinophil count and FeNO on benralizumab effectiveness in clinical practice: An ORBE II subanalysis
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 39814271
dc.relation.publisherversion https://linkinghub.elsevier.com/retrieve/pii/S0954611125000022
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1016/j.rmed.2025.107940
dc.journal.title Respiratory Medicine
dc.identifier.essn 1532-3064


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