Real-Life Performance of Mepolizumab in T2-High Severe Refractory Asthma with the Overlapping Eosinophilic-Allergic Phenotype.
Ruperto González-PérezPaloma Poza-GuedesElena Mederos-LuisInmaculada Sánchez-MachínPublished in: Biomedicines (2022)
Severe asthma (SA) is categorized into multiple overlapping phenotypes and clinical characteristics driven by complex mechanistic inflammatory pathways. Mepolizumab is a human monoclonal antibody effectively targeting interleukin-5 in severe eosinophilic asthma. However, the eligibility of biologics in coincident SA phenotypes is still unclear. We assessed the efficacy and safety of mepolizumab in real-life patients with the overlapping T2-high SA endotype. This was a phase IV, single-centre observational cohort study including patients with severe refractory T2-high asthma in treatment with mepolizumab. After 12 months of treatment with mepolizumab, significant improvements ( p < 0.0001) in asthma control and lung function were recorded. Rates of clinically significant annual asthma exacerbation were also decreased by 71.22% after 52-week therapy with mepolizumab ( p < 0.001) associated with a reduction in the mean daily dose of oral corticosteroids. Two patients (3.27%) had to discontinue mepolizumab due to musculoskeletal disorders with no severe safety issues reported. The use of mepolizumab as an add-on therapy in routine clinical practice was safely associated with significant clinical and functional in the overlapping eosinophilic-and-allergic SA phenotype. The current data should support clinical and therapeutic decision-making in this T2-high SA endotype.
Keyphrases
- lung function
- chronic obstructive pulmonary disease
- allergic rhinitis
- cystic fibrosis
- air pollution
- clinical practice
- monoclonal antibody
- early onset
- end stage renal disease
- physical activity
- drug induced
- intensive care unit
- prognostic factors
- deep learning
- big data
- combination therapy
- chronic rhinosinusitis
- atopic dermatitis
- induced pluripotent stem cells
- electronic health record
- patient reported
- cell therapy
- placebo controlled
- double blind