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Review
. 2025 May 9;18(5):101058.
doi: 10.1016/j.waojou.2025.101058. eCollection 2025 May.

ARIA-Italy multidisciplinary consensus on nasal polyposis and biological treatments: Update 2025

Collaborators, Affiliations
Review

ARIA-Italy multidisciplinary consensus on nasal polyposis and biological treatments: Update 2025

Carlo Lombardi et al. World Allergy Organ J. .

Abstract

In recent years, it was recognized that type-2 inflammation connects nasal polyposis and severe asthma (SA) in addition to other type-2 diseases. Thus, some biological drugs developed for SA appeared to exert a favourable effect also in nasal polyposis. So far, there are several trials supporting this concept; therefore, some monoclonal antibodies already used for SA were assessed also in chronic rhinosinusistis with nasal polyposis (CRSwNP), with promising results. Since different specialists are involved in the management of nasal polyposis (eg, pulmonologists, ENT specialists, allergists, immunologists, pediatricians), it was felt that an updated educational and informative document was needed to better identify the indications of biological therapies in nasal polyposis. We collected the main Italian scientific societies, and prepared (under the umbrella of Allergic Rhinitis and its Impact on Asthma, ARIA) a document endorsed by all societies, to provide a provisional statement for the future use of monoclonal antibodies (MAbs) as a medical treatment for polyposis, possibly associated with SA. The above mentioned document was the first endorsed document on this aspect, and the additional evidence required an update. The current pathogenic knowledge and the experimental evidence are herein reviewed, and some suggestions for a correct prescription and follow-up are provided.

Keywords: ARIA (allergic rhinitis and its impact on asthma); Biological agents; Chronic rhinosinusitis with nasal polyposis; Monoclonal antibodies; Personalized medicine; Severe asthma.

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Conflict of interest statement

The authors report no competing interests.

Figures

Fig. 1
Fig. 1
“CRSwNP pathogenetic mechanisms” from Shah SA et al.
Fig. 2
Fig. 2
“Actual proposals for prescription (A) and discontinuation (B) of biologicals in CRSwNP” from Fokkens WJ et al.
Fig. 2
Fig. 2
“Actual proposals for prescription (A) and discontinuation (B) of biologicals in CRSwNP” from Fokkens WJ et al.
Fig. 3
Fig. 3
“POLINA Consensus criteria for the use of biologics (A) (Legenda: VAS: visual analog scale; SNOT-22: Sino-Nasal Outcome Test-22; HPF: high-power field; N-ERD: NSAID-exacerbated anti-inflammatory drugs. (a) VAS >7 cm and/or SNOT-22 > 50; (b) Opening of affected paranasal sinuses >6 months; (c) Short courses from 5 days at a dose of 0.5–1 mg/kg/d) and for the evaluation of biological treatment at 6 and 12 months (B) (Legenda: (a) See POLINA control criteria; (b) Endoscopic sinus surgery with opening of affected paranasal sinuses; (c) Oral corticosteroids for 5 days at a dose of 0.5–1 mg/kg/d)”. from Alobid I et al.

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