Real-life evaluation of the effectiveness of biologics for chronic rhinosinusitis with nasal polyps in Europe: a Delphi study to define key variables for the INVENT registry

Background: Chronic rhinosinusitis with nasal polyps (CRSwNP) is a persistent inflammatory condition often associated with type 2 inflammation. While biologics are a promising treatment for patients with uncontrolled CRSwNP, real-world evidence is needed to optimize their use. The InternatioNal seVerE CRSwNP (INVENT) registry aims to consolidate data on biologic use in CRSwNP from local and national registries. This study describes the identification of mandatory and optional variables for inclusion in the INVENT registry using a modified Delphi process.

Methods: A narrative literature review was performed to identify variables reported in real-world studies of biologic treatment for CRSwNP. A modified Delphi study was conducted between December 2024 and March 2025 involving 23 experts from Europe and Australia. Experts rated the clinical relevance of candidate variables in two online survey rounds using 9-point Likert scales. A positive response was defined as =70% of respondents rating a variable 7-9 and =15% rating it 1-3. Final agreement on mandatory and optional variables was reached through panel discussion. A validation survey was then conducted across registry centers to assess the feasibility of collecting the selected variables.

Results: The Delphi process resulted in consensus on a core set of mandatory and optional variables across nine domains: demographics, medical history, previous and current biologic therapy, biomarkers, comorbidities, asthma, CRSwNP-specific outcomes, and follow-up variables. The validation survey confirmed that most mandatory variables were available or obtainable across participating centers, supporting the feasibility of data collection.

Conclusions: This international Delphi study identified a consensus-based set of clinically-relevant and feasible variables for inclusion in the INVENT registry. The selected variables reflect current best practices in the management of CRSwNP and will enable robust comparisons of biologic effectiveness in real-world settings. The INVENT registry is well-positioned to inform treatment decisions, optimize use of biologics, and support a personalized approach to CRSwNP care.

Contributors

Vibeke Backer, Eugenio De Corso, Geoffrey Mortuaire, Emmanuel Prokopakis, Anette Drøhse Kjeldsen, Philippe Gevaert, Adam M Chaker, Luisa Azevedo, Christian von Buchwald, Emilie Bequignon, Eliza Brozek-Madry, Jannis Constantinidis, Marjolein Cornet, Wytske J Fokkens, Peter G Gibson, Aleksander Grande Hansen, Joaquim Mullol, Sietze Reitsma, Sanna Toppila-Salmi, Michael B Soyka, Martin Wagenmann, Peter W Hellings

Publication

Journal: Frontiers in Allergy
Volume: 6
Issue:
Pages: -
Year: 2025
DOI: https://doi.org/10.3389/falgy.2025.1680703

Further Study Information

Current Stage: Completed
Date:
Funding source(s): The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by Sanofi and Regeneron.


Health Area

Disease Category: Ear, nose, & throat

Disease Name: Rhinosinusitis , Sinusitis (chronic rhinosinusitis)

Target Population

Age Range: 0 - 100

Sex: Either

Nature of Intervention: Biologic

Stakeholders Involved

- Clinical experts

Study Type

- COS for registry

Method(s)

- Consensus meeting
- Delphi process
- Survey
- Systematic review

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