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EUFOREA consensus on biologics for CRSwNP with or without asthma
Wytske J Fokkens1,2, Valerie Lund3, Claus Bachert2,4,5
1Department of Otorhinolaryngology, Amsterdam University Medical Centres, Location AMC Amsterdam, Amsterdam, The Netherlands.
Novel biologic therapies targeting type 2 inflammation offer new hope for severe chronic rhinosinusitis with nasal polyps (CRSwNP) and asthma. Patient selection is key to effectively integrating these advanced treatments into care pathways.
Area of Science:
- Respiratory Medicine
- Immunology
- Pharmacology
Background:
- Chronic inflammatory respiratory diseases like asthma and chronic rhinosinusitis with nasal polyps (CRSwNP) often exhibit type 2 inflammation.
- Type 2 inflammation is prevalent in CRSwNP and asthma, affecting sinonasal mucosa and/or lungs.
- These conditions frequently coexist, suggesting systemic therapies could benefit both upper and lower airways.
Framework:
- Type 2-targeting biologics (e.g., anti-IgE, anti-IL4Rα, anti-IL5, anti-IL5Rα) are approved for specific asthma phenotypes.
- These biologics are anticipated for CRSwNP treatment, addressing unmet needs in severe disease.
- A multidisciplinary expert meeting convened to discuss the integration of biologics into CRSwNP care pathways, considering comorbid asthma.
Implementation:
- Biologics offer a new treatment modality for patients with severe, uncontrolled type 2 inflammatory respiratory diseases.
- Systemic biological therapy can potentially alleviate pathology in both the upper (sinonasal) and lower (lung) airways.
- The high cost and prevalence necessitate careful patient selection for optimal use of these novel therapies.
Implications:
- Strategic implementation of biologics requires defining patient phenotypes and endotypes for targeted therapy.
- Careful patient selection is paramount for maximizing therapeutic benefit and managing healthcare costs.
- Integrating biologics into care pathways can improve outcomes for patients with complex, comorbid respiratory conditions.
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