Abstract
Purpose of Review
We aimed to reach an Italian multidisciplinary consensus on some crucial aspects of treatment decision making in CRSwNP, following 2 years of clinical experience in order to support specialists in the management of CRSwNP in clinical practice. We addressed issues relating to therapeutic decision-making and shared criteria for the treatment choice, as well as appropriate timing and criteria for evaluating treatment response, and highlighted the need for repeated multidisciplinary assessments.
Recent Findings
A national survey has been conducted recently to understand how rhinology practice has changed in Italy with the advent of biologics and how this affects patients with uncontrolled, severe CRSwNP. Despite the many published consensus documents, practical recommendations, and protocols on the use of biologics in CRSwNP, heterogenous behaviors in practice are still observed mainly conditioned by the novelty of the topic.
Summary
The consensus procedure followed a modified Delphi approach. The scientific board included 18 otorhinolaryngologists and 8 allergists, who selected the 4 main topics to be addressed and developed overall 20 statements. Consensus on these statements was sought by a larger group of 48 additional experts, through two rounds of voting, the first web-based, the second in presence with discussion and possible refinement of the statements. The statements reaching an average score ≥ 7 at the second voting round were approved. Five statements were proposed for each of the following topics: baseline evaluation of patients eligible for biologic therapy; choice between different therapeutic options; assessment of the response to biologic treatment; multidisciplinary management. At the first voting round, 19 out of the 20 statements reached a mean score ≥ 7. Following the discussion and a few consequent amendments, at the second round of voting all the 20 statements were approved.
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Data Availability
No datasets were generated or analysed during the current study.
Change history
20 April 2024
The original version of this paper was updated to correct the family name of Matteo Alicandri Ciufelli.
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Acknowledgements
We would like to thank Renata Perego, MD, an independent medical writer, for her help in drafting the manuscript. We extend our sincere gratitude to all participants who contributed to the Delphi process. Their valuable insights and thoughtful responses have been instrumental in shaping our understanding and decision-making. For that reasons we thank Francesca Anastasi; Roberta Anzivino; Gabriele Arra; Giovanni Bastanza; Elisabetta Bison; Andrea Ciofalo; Maria Angiola Crivellaro; Giuseppe D’agostino; Giulia Dane’; Leandro Maria Dauria; Alessio De Massimi; Albarosa De Pascale; Carla De Vita; Valeria Dell’era; Giovanni Delu; Francesca Di Lallo; Gianluca Fadda; Francesco Fiorino; Cosimo Galletti; Giorgio Oliviero Gallone; Maria Stella Garritani; Angela Gasparini; Alessia Giorli; Luca Guastini; Antonella Loperfido; Lucia Lora; Simonetta Masieri; Claudio Montuori; Patrick Pinter; Davide Paolo Porru; Alessandro Pusateri; Martina Ragusa; Cecilia Rosso; Paolo Russo; Tommaso Saccardo; Giampiero Salonna; Daria Salsi; Mariella Scarano; Federico Sireci; Fabio Sovardi; Paolo Antiuco Uras.
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EDC: conceptualization, writing original draft, resources, methodology, editing, supervision, statements discussion and validation. CP, EC, MC, VS methodology, critical revision, statements discussion and validation. LC, EN, MG, GO, MG, CC, EH, FP, EP, MT, SG, ILM, ST, DM, CC, AM, AV, GB, MAC, PFM, statements discussion and validation, critical revision. GS supervision, statements discussion and validation, critical revision, final approval & editing. All authors have read and agreed to the published final version of the manuscript.
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EDC has received fees for consultation, speaker activity, and advisory boards from Sanofi, Regeneron, GlaxoSmithKline (GSK), Novartis and AstraZeneca. GO has received fees for consultation, speaker activity, and served on advisory boards for Sanofi, GSK, and Novartis. CP has received fees for consultation, speaker activity, advisory boards from Sanofi, Regeneron, GSK, Novartis, Chiesi, Firma. EC has received lecture fees from and participated in experts’ board meetings of GSK, Novartis, Sanofi, NOOS, and AstraZeneca. MC has received speaker and consultancy fees from Astra Zeneca, GSK, and Sanofi. CC has received lecture fees and participated in experts’ board meetings of GSK, Novartis, and Sanofi. G Senna has received speaker fees from Sanofi, AstraZeneca, and GSK. ST fees for lectures and advisory boards for GSK and SANOFI. VS has received lecture fees and participated in experts’ board meetings of GSK, Novartis, Sanofi, and AstraZeneca. MG has received lecture fees and participated in experts’ board meetings of GSK and Sanofi. MT has received consulting fees from Sanofi, GSK, and Novartis. FP has received consulting fees from Sanofi, Novartis, Chiesi, Menarini, Firma, and Deca. FRC has received lecture fees and participated in experts board meetings of GSK, Novartis, and Sanofi. ILM has received lecture fees and participated in experts’ board meetings of Sanofi. The other authors declare no conflict of interest. LC has received fees for consultation, speaker activity, and advisory boards from Sanofi, GlaxoSmithKline (GSK), Novartis, Menarini, Thermofisher, ALK and AstraZeneca. EN has received speaker and consultancy fees from Abbvie, Leo-Pharma, Novartis, Astra Zeneca, GSK, and Sanofi. MAC has received fees for consultation, speaker activity, advisory boards from Sanofi. GB has received lecture fees and participated in experts’ board meetings of Sanofi, GSK, Novartis, Abiogen, Aurora Biopharma. CC has received fees for consultation, speaker activity, and advisory boards from Sanofi, GlaxoSmithKline (GSK), menarini, Chiesi and AstraZeneca. MG has received advisory board fees or speaker fees from GlaxoSmithKline, Novartis, Sanofi-Genzyme, Valeas, DMG Italia, FIRMA, Aurora Biofarma, and Fenix Pharma. EH has received speaker activity and advisory board participation fees from Novartis, GlaxoSmithKline, Sanofi, Regeneron, AstraZeneca, Stallergenes-Greer, Circassia, and Nestlè Purina. AM has received speaker’s fees from Amicus Therapeutics, AstraZeneca, GSK, Novartis, Sanofi and Takeda and honoraria for attending advisory board meetings with, AstraZeneca, GSK, Novartis, Sanofi and Chiesi. AV has received speaker’s fees from AstraZeneca, GSK, Novartis, Sanofi and Chiesi and honoraria for attending advisory board meetings with, AstraZeneca, GSK, Novartis, Sanofi. PFM has received lecture fees and participated in experts board meetings of GSK and Sanofi. EP, SG, DM, has none conflict of interest. GS has received speaker fee and research grant by AstraZeneca, GSK, Novartis, Sanofi.
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De Corso, E., Pipolo, C., Caminati, M. et al. Multidisciplinary Decision-Making—ITAlian Consensus After Two Years of Real Practice on the Management of Severe Uncontrolled CRSwNP by Biologics (ITACA Study). Curr Allergy Asthma Rep 24, 143–154 (2024). https://doi.org/10.1007/s11882-024-01135-z
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DOI: https://doi.org/10.1007/s11882-024-01135-z