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Dupilumab Extended Interval Dosing in Chronic Rhinosinusitis With Nasal Polyps: A Systematic Review and Meta-analysis
Abdulsalam Alqutub1, Amr I Herzallah2, Sulafa Alqutub3
1Department of Otorhinolaryngology-Head and Neck Surgery, Makkah Health Cluster, Makkah, Saudi Arabia.
Summary
Extending dupilumab dosing to every four weeks (Q4W) maintains disease control in chronic rhinosinusitis with nasal polyps (CRSwNP). This dosing interval is effective after standard treatment, with potential for longer intervals in some patients.
Area of Science:
- Immunology
- Otolaryngology
- Pharmacology
Background:
- Chronic rhinosinusitis with nasal polyps (CRSwNP) is an inflammatory upper airway disease.
- Dupilumab, an interleukin-4 receptor alpha antagonist, is effective for CRSwNP.
- Optimizing dupilumab dosing intervals may improve patient management and reduce treatment burden.
Purpose of the Study:
- To assess if extending dupilumab dosing intervals beyond every two weeks (Q2W) maintains disease control in CRSwNP patients.
- To evaluate the impact of extended dupilumab dosing on clinical, radiologic, and biomarker outcomes.
- To explore the feasibility of further dose spacing (e.g., Q6W-Q12W) in select CRSwNP individuals.
Main Methods:
- Systematic literature search of PubMed, Scopus, Cochrane Library, and Web of Science up to September 2025.
- Inclusion of studies where adults with CRSwNP switched from dupilumab 300 mg Q2W to extended intervals (≥Q4W).
- Random-effects meta-analyses synthesized sinonasal, radiologic, and biomarker outcomes; risk of bias assessed using RoB2 and NIH tools.
Main Results:
- Nineteen studies involving 1075 patients were analyzed; nine contributed to quantitative synthesis.
- Extended Q4W dupilumab dosing maintained disease control with non-significant changes in SNOT-22, nasal congestion, olfaction, polyp score, and Lund-Mackay scores.
- A significant decrease in eosinophils was observed (-0.13 × 10⁹/L; P = .047); subgroup analyses showed no significant difference in clinical outcomes between 6- and 12-month induction periods.
Conclusions:
- Extending dupilumab dosing to Q4W is effective in maintaining clinical stability for CRSwNP patients after 6-12 months of standard therapy.
- Further extension to Q6W-Q12W may be feasible in specific patient populations.
- Controlled trials are needed to establish optimal tapering strategies and identify predictors for successful dose spacing.