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Current Goals of NSAID-ERD Management: Patient-Centered Approaches Involving NSAID Desensitization With and Without
Irina Bobolea1, Jan Hagemann2, Marek Sanak3
1Severe Asthma Unit, Allergy Department, Hospital Clinic Barcelona, FRCB-IDIBAPS, Barcelona, Catalonia, Spain; CIBER of Respiratory Diseases (CIBERES), Madrid, Spain.
Nonsteroidal anti-inflammatory drug-exacerbated respiratory disease (NSAID-ERD) management now includes biologics, offering an alternative to aspirin therapy after desensitization (ATAD). Biologics show promise, but ATAD remains relevant, especially considering NSAID tolerance restoration.
Area of Science:
- Immunology
- Respiratory Medicine
- Pharmacology
Background:
- Nonsteroidal anti-inflammatory drug-exacerbated respiratory disease (NSAID-ERD) traditionally managed with NSAID avoidance, medications, and surgery.
- Severe asthma and chronic rhinosinusitis with nasal polyps (CRSwNP) are often type 2, eosinophilic diseases.
- Biologics targeting type 2 inflammation offer new therapeutic avenues.
Purpose of the Study:
- To review the role of aspirin therapy after desensitization (ATAD) in NSAID-ERD.
- To compare biologic therapies with ATAD for NSAID-ERD.
- To discuss considerations for ATAD even with available type 2 biologics.
Main Methods:
- Review of existing literature on NSAID-ERD treatments.
- Analysis of clinical outcomes for biologics (e.g., dupilumab, omalizumab) in NSAID-ERD.
- Comparison of patient preferences for biologics versus ATAD.
Main Results:
- Biologics targeting IgE, IL-5, IL-4, and IL-13 are effective for severe asthma and CRSwNP in NSAID-ERD.
- Dupilumab shows greater efficacy in NSAID-ERD patients compared to aspirin-tolerant individuals.
- Omalizumab rapidly reduces inflammatory mediators and may restore aspirin tolerance in some patients.
Conclusions:
- Biologics represent a significant alternative to ATAD, often favored by patients.
- ATAD remains a consideration, particularly when complete NSAID tolerance restoration is a goal.
- Patient-centered care should guide treatment decisions, weighing biologic efficacy against ATAD benefits.
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