# Effectiveness and Safety of Dupilumab in Patients with Chronic Rhinosinusitis with Nasal Polyps and Associated T2 Comorbidities: One-Year Real Life Round

**Authors:** Eustachio Nettis, Rossella Casella, Elisabetta Di Leo, Ippolita Zaza, Fabio Lodi Rizzini, Alessandro Vrenna, Luisa Brussino, Irene Ridolfi, Laura Bonzano, Lia Ginaldi, Ernesto Aitella, Vincenzo Patella, Roberta Zunno, Massimo Triggiani, Isabella Carrieri, Nicola Antonio Adolfo Quaranta, Lucia Iannuzzi, Francesca Serena Romano, Erminia Ridolo, Alessandro Barone, Angela Maria D’Uggento, Valentina D’Aiuto, Aikaterini Detoraki

PMC · DOI: 10.3390/jcm15041373 · Journal of Clinical Medicine · 2026-02-10

## TL;DR

This study shows that dupilumab is effective and safe for treating chronic rhinosinusitis with nasal polyps and related type 2 immune conditions over one year.

## Contribution

The study provides real-world evidence of dupilumab's long-term effectiveness and safety in patients with CRSwNP and T2 comorbidities.

## Key findings

- Dupilumab significantly improved symptoms across multiple type 2 inflammatory conditions.
- No new safety concerns were observed during the 52-week treatment period.
- Patients showed sustained clinical improvements in nasal, respiratory, and skin-related outcomes.

## Abstract

Background/Objectives: Chronic rhinosinusitis with nasal polyps (CRSwNP) represents a common and debilitating inflammatory disorder primarily driven by type 2 immune mechanisms. Its frequent overlap with asthma, allergic rhinoconjunctivitis and atopic dermatitis highlights the need for therapeutic strategies able to address multimorbidity within the same pathogenic spectrum. The development of monoclonal antibodies targeting signaling pathways provides an effective and well-tolerated option that addresses common comorbidities. Targeting the IL-4 receptor alpha subunit, dupilumab is a completely human IgG4 monoclonal antibody that reduces type 2 inflammation in many organ systems by blocking IL-4 and IL-13 signaling. This study aimed to assess the long-term effectiveness and safety of dupilumab in a real-world cohort of patients with severe CRSwNP, stratified according to the presence of common type 2 comorbidities, over a 52-week treatment period. Methods: We conducted a prospective, multicenter, observational study across ten Italian secondary care centers for Allergy and Clinical Immunology and Otolaryngology. All participating centers were affiliated with the Italian Society of Allergy, Asthma and Clinical Immunology (SIAAIC). Enrolled adult subjects with severe CRSwNP received dupilumab treatment in the context of standard care for 52 weeks. Several efficacy parameters were used. Results: A significant improvement was detected for all the applied efficacy parameters, i.e., 22-item Sinonasal Outcome Test (SNOT-22) and bilateral endoscopic nasal polyp (NPS) scores for CRSwNP, Rhinitis Control Scoring System (RCSS) and Rhinoconjunctivitis Quality of Life Questionnaire (RQLQ) scores for allergic perennial rhinitis, Forced Expiratory Volume in the first second (FEV1) and Asthma Quality of Life Questionnaire (AQLQ) scores for asthma, Eczema Area and Severity Index (EASI), Atopic Dermatitis Control Toll (ADCT) and Dermatology Life Quality Index (DLQI) scores for AD. Dupilumab was well-tolerated, with no new safety signals. Conclusions: This multicenter real-world study demonstrates that dupilumab provides sustained, clinically meaningful, and safe benefits for patients with severe CRSwNP and coexisting type 2 comorbidities, supporting its role as an integrated therapeutic option in precision management of type 2 inflammatory diseases.

## Linked entities

- **Proteins:** IL4 (interleukin 4), IL13 (interleukin 13)
- **Diseases:** asthma (MONDO:0004979), atopic dermatitis (MONDO:0004980)

## Full-text entities

- **Genes:** IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, IL4R (interleukin 4 receptor) [NCBI Gene 3566] {aka CD124, IL-4RA, IL4RA}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}
- **Diseases:** type 2 inflammatory diseases (MESH:C563310), injury to (MESH:D014947), disease (MESH:D004194), inflammatory (MESH:D007249), atopic (MESH:C566404), sleep disturbance (MESH:D012893), Eczema (MESH:D004485), skin disease (MESH:D012871), conjunctivitis (MESH:D003231), AD (MESH:D000544), congestion (MESH:D002311), Nasal congestion (MESH:D009668), allergic rhinitis (MESH:D065631), Rhinoconjunctivitis (OMIM:613207), sinonasal disease (MESH:C535701), Dermatology (MESH:D000168), Asthma (MESH:D001249), Loss of smell (MESH:D000086582), eosinophilia (MESH:D004802), food allergy (MESH:D005512), Rhinitis (MESH:D012220), anterior/posterior rhinorrhea (MESH:D020759), polyp (MESH:D011127), Urticaria (MESH:D014581), PAR (MESH:D012221), type 2 diseases (MESH:C536595), Chronic rhinosinusitis with nasal polyposis (MESH:D000092562), AD (MESH:D003876), smell impairment (MESH:D000857), pruritus (MESH:D011537), CRSwNP (MESH:D009298)
- **Chemicals:** INS (-), Dupilumab (MESH:C582203)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12941292/full.md

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Source: https://tomesphere.com/paper/PMC12941292