Severe Pediatric Asthma Therapy: Mepolizumab
There is a growing need for advanced treatment in children with persistent and severe asthma symptoms. As a matter of fact, between 2 and 5% of asthmatic children experience repeated hospitalizations and poor quality of life despite optimized treatment with inhaled glucocorticoid plus a second contr...
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Published in: | Frontiers in pediatrics Vol. 10; p. 920066 |
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Abstract | There is a growing need for advanced treatment in children with persistent and severe asthma symptoms. As a matter of fact, between 2 and 5% of asthmatic children experience repeated hospitalizations and poor quality of life despite optimized treatment with inhaled glucocorticoid plus a second controller. In this scenario, mepolizumab, a humanized monoclonal antibody, has proven to be effective in controlling eosinophil proliferation by targeting interleukin-5 (IL-5), a key mediator of eosinophil activation pathways. Mepolizumab is approved since 2015 for adults at a monthly dose of 100 mg subcutaneously and it has been approved for patients ≥ 6 years of age in 2019. Especially in children aged 6 to 11 years, mepolizumab showed a greater bioavailability, with comparable pharmacodynamics parameters as in the adult population. The recommended dose of 40 mg every 4 weeks for children aged 6 through 11 years, and 100 mg for patients ≥ 12 years provides appropriate concentration and proved similar therapeutic effects as in the adult study group. A marked reduction in eosinophil counts clinically reflects a significant improvement in asthma control as demonstrated by validated questionnaires, reduction of exacerbation rates, and the number of hospitalizations. Finally, mepolizumab provides a safety and tolerability profile similar to that observed in adults with adverse events mostly of mild or moderate severity. The most common adverse events were headache and injection-site reaction. In conclusion, mepolizumab can be considered a safe and targeted step-up therapy for severe asthma with an eosinophilic phenotype in children and adolescents. |
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AbstractList | There is a growing need for advanced treatment in children with persistent and severe asthma symptoms. As a matter of fact, between 2 and 5% of asthmatic children experience repeated hospitalizations and poor quality of life despite optimized treatment with inhaled glucocorticoid plus a second controller. In this scenario, mepolizumab, a humanized monoclonal antibody, has proven to be effective in controlling eosinophil proliferation by targeting interleukin-5 (IL-5), a key mediator of eosinophil activation pathways. Mepolizumab is approved since 2015 for adults at a monthly dose of 100 mg subcutaneously and it has been approved for patients ≥ 6 years of age in 2019. Especially in children aged 6 to 11 years, mepolizumab showed a greater bioavailability, with comparable pharmacodynamics parameters as in the adult population. The recommended dose of 40 mg every 4 weeks for children aged 6 through 11 years, and 100 mg for patients ≥ 12 years provides appropriate concentration and proved similar therapeutic effects as in the adult study group. A marked reduction in eosinophil counts clinically reflects a significant improvement in asthma control as demonstrated by validated questionnaires, reduction of exacerbation rates, and the number of hospitalizations. Finally, mepolizumab provides a safety and tolerability profile similar to that observed in adults with adverse events mostly of mild or moderate severity. The most common adverse events were headache and injection-site reaction. In conclusion, mepolizumab can be considered a safe and targeted step-up therapy for severe asthma with an eosinophilic phenotype in children and adolescents. |
Author | Porcaro, Federica Peri, Francesca Cutrera, Renato Florio, Olivia Onofri, Alessandro Ullmann, Nicola Profeti, Elisa |
AuthorAffiliation | 3 Respiratory Medicine Unit, University “Magna Graecia” of Catanzaro , Catanzaro , Italy 1 Pediatric Pulmonology & Respiratory Intermediate Care Unit, Sleep, and Long Term Ventilation Unit, Academic Department of Pediatrics (DPUO), Bambino Gesù Children's Hospital, IRCCS , Rome , Italy 2 Department of Medicine, Surgery, and Health Sciences, University of Trieste , Trieste , Italy |
AuthorAffiliation_xml | – name: 3 Respiratory Medicine Unit, University “Magna Graecia” of Catanzaro , Catanzaro , Italy – name: 2 Department of Medicine, Surgery, and Health Sciences, University of Trieste , Trieste , Italy – name: 1 Pediatric Pulmonology & Respiratory Intermediate Care Unit, Sleep, and Long Term Ventilation Unit, Academic Department of Pediatrics (DPUO), Bambino Gesù Children's Hospital, IRCCS , Rome , Italy |
Author_xml | – sequence: 1 givenname: Nicola surname: Ullmann fullname: Ullmann, Nicola – sequence: 2 givenname: Francesca surname: Peri fullname: Peri, Francesca – sequence: 3 givenname: Olivia surname: Florio fullname: Florio, Olivia – sequence: 4 givenname: Federica surname: Porcaro fullname: Porcaro, Federica – sequence: 5 givenname: Elisa surname: Profeti fullname: Profeti, Elisa – sequence: 6 givenname: Alessandro surname: Onofri fullname: Onofri, Alessandro – sequence: 7 givenname: Renato surname: Cutrera fullname: Cutrera, Renato |
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Copyright | Copyright © 2022 Ullmann, Peri, Florio, Porcaro, Profeti, Onofri and Cutrera. 2022 Ullmann, Peri, Florio, Porcaro, Profeti, Onofri and Cutrera |
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Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 This article was submitted to Pediatric Pulmonology, a section of the journal Frontiers in Pediatrics Edited by: Mario Barreto, Sapienza University of Rome, Italy Reviewed by: Garry M. Walsh, University of Aberdeen, United Kingdom; Kestutis Malakauskas, Lithuanian University of Health Sciences, Lithuania; Zorica Momcilo Zivkovic, University Hospital Center Dr Dragiša Mišović, Serbia |
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StartPage | 920066 |
SubjectTerms | adolescents asthma biologics children mepolizumab Pediatrics treatment |
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Title | Severe Pediatric Asthma Therapy: Mepolizumab |
URI | https://search.proquest.com/docview/2691459317 https://pubmed.ncbi.nlm.nih.gov/PMC9283570 https://doaj.org/article/e609d734d9c049749723603e0d9da31d |
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