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Benralizumab in severe eosinophilic asthma: A real-world, single-center, observational study from Mexico
Miguel Reyes, José Luis; López Estrada, Erika del Carmen; Arroyo Rojas, Monserrat; Salas Hernández, Jorge; Castañeda Valdivia, Mauricio; Escobar Preciado, Monserrat; Cano Salas, Maria del Carmen.
Afiliación
  • Miguel Reyes, José Luis; National Institute of Respiratory Diseases Ismael Cosio Villegas. Mexico City. Mexico
  • López Estrada, Erika del Carmen; National Institute of Respiratory Diseases Ismael Cosio Villegas. Mexico City. Mexico
  • Arroyo Rojas, Monserrat; National Institute of Respiratory Diseases Ismael Cosio Villegas. Mexico City. Mexico
  • Salas Hernández, Jorge; National Institute of Respiratory Diseases Ismael Cosio Villegas. Mexico City. Mexico
  • Castañeda Valdivia, Mauricio; National Institute of Respiratory Diseases Ismael Cosio Villegas. Mexico City. Mexico
  • Escobar Preciado, Monserrat; National Institute of Respiratory Diseases Ismael Cosio Villegas. Mexico City. Mexico
  • Cano Salas, Maria del Carmen; National Institute of Respiratory Diseases Ismael Cosio Villegas. Mexico City. Mexico
Allergol. immunopatol ; 51(6): 8 -15, 2023. tab, graf
Article en En | IBECS | ID: ibc-227303
Biblioteca responsable: ES1.1
Ubicación: ES15.1 - BNCS
ABSTRACT

Introduction:

Urbanization has increased the prevalence of asthma in lower- and middle-income countries. Severe eosinophilic asthma (SEA), a subtype of asthma, can be refractory to standard therapy. Biologics such as benralizumab target interleukin-5 and have demonstrated effectiveness in managing SEA. There exists no real-world evidence on the effectiveness of benralizumab in Mexico. Therefore, this study presents data on the role of benralizumab in managing SEA in Mexican patients.

Objective:

The effectiveness of benralizumab on the quality of life (QoL), asthma control, lung function, symptoms of asthma, and benralizumab’s safety profile were assessed.

Methods:

The study sample comprised 10 patients with SEA treated with a subcutaneous (SC) administration of benralizumab 30 mg once in 4 weeks for the first three doses followed by a dose every 8 weeks for 2 years. Laboratory tests, resting spirometry, and skin prick tests were conducted. Levels of fractional exhaled nitric oxide (FeNO) were evaluated, when possible, with the intent to phenotype asthma, as T2 high or non-T2, before starting benralizumab therapy. The Asthma Quality of Life Questionnaire (AQLQ), Asthma Control Questionnaire (ACQ), and Asthma Control Test (ACT) were administered to evaluate the effectiveness of benralizumab on asthma control and QoL.

Results:

All patients showed significant symptom control, QoL, and lung function over 2 years. Mild adverse effects, such as headache and arthralgia, were observed.

Conclusion:

Benralizumab appears to be a promising agent in controlling SEA. This study has focused on measuring tangible outcomes, such as a reduction in symptoms, a reduction in exacerbation, and an improvement in QoL. Thus, benralizumab may constitute an important addition to the arsenal of medications against SEA (AU)
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Texto completo: 1 Banco de datos: IBECS Asunto principal: Asma / Antiasmáticos / Anticuerpos Monoclonales Humanizados Límite: Adult / Female / Humans / Male País/Región como asunto: Mexico Idioma: En Revista: Allergol. immunopatol Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: IBECS Asunto principal: Asma / Antiasmáticos / Anticuerpos Monoclonales Humanizados Límite: Adult / Female / Humans / Male País/Región como asunto: Mexico Idioma: En Revista: Allergol. immunopatol Año: 2023 Tipo del documento: Article