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Heterogeneity in the use of biologics for severe asthma in Europe: a SHARP ERS study

Heterogeneity in the use of biologics for severe asthma in Europe: a SHARP ERS study
Heterogeneity in the use of biologics for severe asthma in Europe: a SHARP ERS study

Introduction: treatment with biologics for severe asthma is informed by international and national guidelines and defined by national regulating bodies, but how these drugs are used in real-life is unknown.

Materials and methods: the European Respiratory Society (ERS) SHARP Clinical Research Collaboration conducted a three-step survey collecting information on asthma biologics use in Europe. Five geographically distant countries defined the survey questions, focusing on seven end-points: biologics availability and financial issues, prescription and administration modalities, inclusion criteria, continuation criteria, switching biologics, combining biologics and evaluation of corticosteroid toxicity. The survey was then sent to SHARP National Leads of 28 European countries. Finally, selected questions were submitted to a broad group of 263 asthma experts identified by national societies.

Results: availability of biologics varied between countries, with 17 out of 28 countries having all five existing biologics. Authorised prescribers (pulmonologists and other specialists) also differed. In-hospital administration was the preferred deliverance modality. While exacerbation rate was used as an inclusion criterion in all countries, forced expiratory volume in 1 s was used in 46%. Blood eosinophils were an inclusion criterion in all countries for interleukin-5 (IL-5)-targeted and IL-4/IL-13-targeted biologics, with varying thresholds. There were no formally established criteria for continuing biologics. Reduction in exacerbations represented the most important benchmark, followed by improvement in asthma control and quality of life. Only 73% (191 out of 263) of surveyed clinicians assessed their patients for corticosteroid-induced toxicity.

Conclusion: our study reveals important heterogeneity in the use of asthma biologics across Europe. To what extent this impacts on clinical outcomes relevant to patients and healthcare services needs further investigation.

2312-0541
Frix, Anne-Noelle
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Heaney, Liam G.
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Dahlén, Barbro
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Mihaltan, Florin
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Sergejeva, Svetlana
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Popović-Grle, Sanja
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Lehtimäki, Lauri
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Bourdin, Arnaud
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Korn, Stephanie
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Zervas, Eleftherios
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Csoma, Zsuzsanna
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Lúðvíksdóttir, Dora
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Butler, Marcus
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Canonica, Giorgio Walter
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Grisle, Ineta
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Bieksiene, Kristina
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Chaves Loureiro, Claudia
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Nenasheva, Natalia M
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Gemicioglu, Bilun
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Bossios, Apostolos
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Porsbjerg, Celeste M
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Bel, Elisabeth H.
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Djukanovic, Ratko
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Louis, Renaud
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Frix, Anne-Noelle
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Heaney, Liam G.
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Dahlén, Barbro
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Mihaltan, Florin
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Sergejeva, Svetlana
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Sedlak, Vratislav
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Korn, Stephanie
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Bossios, Apostolos
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Porsbjerg, Celeste M
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Bel, Elisabeth H.
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Djukanovic, Ratko
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Louis, Renaud
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Frix, Anne-Noelle, Heaney, Liam G., Dahlén, Barbro, Mihaltan, Florin, Sergejeva, Svetlana, Popović-Grle, Sanja, Sedlak, Vratislav, Lehtimäki, Lauri, Bourdin, Arnaud, Korn, Stephanie, Zervas, Eleftherios, Csoma, Zsuzsanna, Lúðvíksdóttir, Dora, Butler, Marcus, Canonica, Giorgio Walter, Grisle, Ineta, Bieksiene, Kristina, Ten Brinke, Anneke, Kuna, Piotr, Chaves Loureiro, Claudia, Nenasheva, Natalia M, Lazic, Zorica, Škrgat, Sabina, Ramos-Barbon, David, Leuppi, Joerg, Gemicioglu, Bilun, Bossios, Apostolos, Porsbjerg, Celeste M, Bel, Elisabeth H., Djukanovic, Ratko and Louis, Renaud (2022) Heterogeneity in the use of biologics for severe asthma in Europe: a SHARP ERS study. ERJ Open Research, 8 (4), [00273-2022]. (doi:10.1183/23120541.00273-2022).

Record type: Article

Abstract

Introduction: treatment with biologics for severe asthma is informed by international and national guidelines and defined by national regulating bodies, but how these drugs are used in real-life is unknown.

Materials and methods: the European Respiratory Society (ERS) SHARP Clinical Research Collaboration conducted a three-step survey collecting information on asthma biologics use in Europe. Five geographically distant countries defined the survey questions, focusing on seven end-points: biologics availability and financial issues, prescription and administration modalities, inclusion criteria, continuation criteria, switching biologics, combining biologics and evaluation of corticosteroid toxicity. The survey was then sent to SHARP National Leads of 28 European countries. Finally, selected questions were submitted to a broad group of 263 asthma experts identified by national societies.

Results: availability of biologics varied between countries, with 17 out of 28 countries having all five existing biologics. Authorised prescribers (pulmonologists and other specialists) also differed. In-hospital administration was the preferred deliverance modality. While exacerbation rate was used as an inclusion criterion in all countries, forced expiratory volume in 1 s was used in 46%. Blood eosinophils were an inclusion criterion in all countries for interleukin-5 (IL-5)-targeted and IL-4/IL-13-targeted biologics, with varying thresholds. There were no formally established criteria for continuing biologics. Reduction in exacerbations represented the most important benchmark, followed by improvement in asthma control and quality of life. Only 73% (191 out of 263) of surveyed clinicians assessed their patients for corticosteroid-induced toxicity.

Conclusion: our study reveals important heterogeneity in the use of asthma biologics across Europe. To what extent this impacts on clinical outcomes relevant to patients and healthcare services needs further investigation.

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00273-2022.full - Version of Record
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More information

Accepted/In Press date: 8 August 2022
Published date: 24 October 2022
Additional Information: Funding Information: The SHARP National Leads survey revealed that corticosteroid-induced toxicity was assessed in 20 countries (mainly by clinical evaluation and cortisol blood levels). This was supported by data extracted from the Experts Broad Survey, which showed evaluation by 70% of experts. Cortisol blood level and clinical evaluation were also the most commonly used assessment modalities. Funding Information: Support statement: The SHARP CRC has been supported by financial and other contributions from the following consortium partners: European Respiratory Society, GlaxoSmithKline Research and Development Limited, Chiesi Farmaceutici SPA, Novartis Pharma AG, Sanofi-Genzyme Corporation, and Teva Branded Pharmaceutical Products R&D, Inc. Funding information for this article has been deposited with the Crossref Funder Registry. Publisher Copyright: © The authors 2022.

Identifiers

Local EPrints ID: 473343
URI: http://eprints.soton.ac.uk/id/eprint/473343
ISSN: 2312-0541
PURE UUID: 76787975-994a-4a7f-bf26-26f70cf820c9
ORCID for Ratko Djukanovic: ORCID iD orcid.org/0000-0001-6039-5612

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Date deposited: 16 Jan 2023 17:43
Last modified: 17 Mar 2024 02:34

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Contributors

Author: Anne-Noelle Frix
Author: Liam G. Heaney
Author: Barbro Dahlén
Author: Florin Mihaltan
Author: Svetlana Sergejeva
Author: Sanja Popović-Grle
Author: Vratislav Sedlak
Author: Lauri Lehtimäki
Author: Arnaud Bourdin
Author: Stephanie Korn
Author: Eleftherios Zervas
Author: Zsuzsanna Csoma
Author: Dora Lúðvíksdóttir
Author: Marcus Butler
Author: Giorgio Walter Canonica
Author: Ineta Grisle
Author: Kristina Bieksiene
Author: Anneke Ten Brinke
Author: Piotr Kuna
Author: Claudia Chaves Loureiro
Author: Natalia M Nenasheva
Author: Zorica Lazic
Author: Sabina Škrgat
Author: David Ramos-Barbon
Author: Joerg Leuppi
Author: Bilun Gemicioglu
Author: Apostolos Bossios
Author: Celeste M Porsbjerg
Author: Elisabeth H. Bel
Author: Renaud Louis

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