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Real-World Effectiveness of Benralizumab in Severe Eosinophilic Asthma.
Kavanagh, Joanne E; Hearn, Andrew P; Dhariwal, Jaideep; d'Ancona, Gráinne; Douiri, Abdel; Roxas, Cris; Fernandes, Mariana; Green, Linda; Thomson, Louise; Nanzer, Alexandra M; Kent, Brian D; Jackson, David J.
Afiliación
  • Kavanagh JE; Guy's Severe Asthma Centre, Guy's and St Thomas' Hospitals, London, England; Asthma UK Centre, King's College London, London, England.
  • Hearn AP; Guy's Severe Asthma Centre, Guy's and St Thomas' Hospitals, London, England; Asthma UK Centre, King's College London, London, England.
  • Dhariwal J; Guy's Severe Asthma Centre, Guy's and St Thomas' Hospitals, London, England.
  • d'Ancona G; Guy's Severe Asthma Centre, Guy's and St Thomas' Hospitals, London, England.
  • Douiri A; Department of Medical Statistics, King's College London, London, England.
  • Roxas C; Guy's Severe Asthma Centre, Guy's and St Thomas' Hospitals, London, England.
  • Fernandes M; Guy's Severe Asthma Centre, Guy's and St Thomas' Hospitals, London, England.
  • Green L; Guy's Severe Asthma Centre, Guy's and St Thomas' Hospitals, London, England.
  • Thomson L; Guy's Severe Asthma Centre, Guy's and St Thomas' Hospitals, London, England.
  • Nanzer AM; Guy's Severe Asthma Centre, Guy's and St Thomas' Hospitals, London, England.
  • Kent BD; Department of Respiratory Medicine, St. James' Hospital, Dublin, Ireland; School of Medicine, Trinity College, Dublin, Ireland.
  • Jackson DJ; Guy's Severe Asthma Centre, Guy's and St Thomas' Hospitals, London, England; Asthma UK Centre, King's College London, London, England. Electronic address: David.jackson@gstt.nhs.uk.
Chest ; 159(2): 496-506, 2021 02.
Article en En | MEDLINE | ID: mdl-32882249
ABSTRACT

BACKGROUND:

Benralizumab is an IL5-receptor monoclonal antibody licensed for the treatment of severe eosinophilic asthma (SEA). It has demonstrated efficacy in clinical trials in reducing asthma exacerbation rates and maintenance oral corticosteroids (mOCSs). RESEARCH QUESTION What is the real-world effectiveness of benralizumab and what baseline characteristics are associated with response to therapy? STUDY DESIGN AND

METHODS:

We assessed outcomes in all SEA patients who began benralizumab treatment at our specialist center. At each dosing visit, exacerbation history, mOCS dose, spirometry, and Asthma Control Questionnaire (ACQ6) and Mini-Asthma Quality of Life Questionnaire (mAQLQ) scores were recorded. Response to treatment was defined as a reduction of ≥ 50% in annualized exacerbation rate (AER) or in mOCS dose after 48 weeks of treatment. Super response was defined as zero exacerbations and no mOCSs for asthma.

RESULTS:

One hundred thirty patients were included in the analysis. At 48 weeks, a 72.8% reduction in AER was noted, from 4.92 ± 3.35 per year in the year preceding biologic treatment to 1.34 ± 1.71 per year (P < .001), including 57 patients (43.8%) who were exacerbation-free with benralizumab. In those receiving mOCSs (n = 74 [56.9%]), the median daily prednisolone dose fell from 10 mg (interquartile range, 5-20 mg) to 0 mg (interquartile range, 0-5 mg; P < .001), and 38 of 74 patients (51.4%) were able to discontinue mOCS therapy. Clinically and statistically significant improvements were found in ACQ6 scores, mAQLQ scores, and FEV1. Overall, 51 patients (39%) met the super responder definition and 112 patients (86%) met the responder definition. The optimal regression model of super responders vs other responders included baseline characteristics associated with a strongly eosinophilic phenotype and less severe disease. Eighteen patients (13.8%) were nonresponders to benralizumab. Evidence of chronic airway infection was observed in 6 of 18 patients, and an increase in the blood eosinophil count consistent with the development of anti-drug antibodies was observed in 5 of 18 patients.

INTERPRETATION:

In a large real-world SEA cohort, benralizumab led to significant improvements in all clinical outcome measures. A lack of response was seen in a minority of patients and should be a focus for future investigation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Eosinofilia Pulmonar / Asma / Antiasmáticos / Anticuerpos Monoclonales Humanizados Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Límite: Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Chest Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Eosinofilia Pulmonar / Asma / Antiasmáticos / Anticuerpos Monoclonales Humanizados Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Límite: Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Chest Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido