TY - JOUR
T1 - Attitudes and Practices Regarding Dosing Interval Extension of Biologics in Severe Asthma
T2 - A Nationwide Survey and Real-World Data From the Dutch RAPSODI Registry
AU - Marijnissen, Camiel J.M.
AU - Sont, Jacob K.
AU - Meulmeester, Fleur L.
AU - Wouters, Michel W.J.M.
AU - Braunstahl, Gert Jan
AU - Aldenkamp, Arnoud F.
AU - Hashimoto, Simone
AU - Kroes, Johannes A.
AU - van den Akker-van Marle, M. Elske
AU - Steyerberg, Ewout W.
AU - van Bodegom-Vos, Leti
AU - van Bezouw, Maarten J.
AU - Hilvering, Bart
AU - Weersink, Els J.M.
AU - van der Sar-van der Brugge, Simone
AU - Fieten, Karin B.
AU - Beukert, Annelies
AU - Retera, Jeroen M.A.M.
AU - Oud, Karen T.M.
AU - van der Meer, Renske
AU - Patberg, Kornelis W.
AU - Macken, Thomas
AU - de Visser, Veerle L.
AU - Conemans, Lennart H.
AU - van Velzen, Edwin
AU - van Veen, Ilonka H.
AU - van Huisstede, Astrid
AU - Romme, Elisabeth A.P.M.
AU - Amelink, Marijke
AU - van Ruitenbeek, Charlotte A.
AU - ten Brinke, Anneke
AU - Kappen, Jasper H.
N1 - Funding Information:
Conflicts of interest: J. K. Sont has received nonrestricted research grants from AstraZeneca , RAPSODI Foundation, and ZonMW. G.-J. Braunstahl has received grant/research support for consultations and/or speaking at conferences from Novartis , Sanofi , GlaxoSmithKline (GSK), AstraZeneca, ALK , Teva , and Chiesi. J. A. Kroes reports a grant from AstraZeneca, unrelated to this work. B. Hilvering received consultation fees from GSK, AstraZeneca, and Sanofi. A. Beukert received hospitality compensation from GSK and Sanofi. L. H. Conemans has received grant/research support for consultations and/or speaking at conferences from GSK, AstraZeneca, and Sanofi. E. A. P. M. Romme received a consultation fee from AstraZeneca for serving on an advisory board on cardiopulmonary risk in COPD. A. t. Brinke has received nonrestricted research grants from AstraZeneca, TEVA, RAPSODI Foundation, and ZonMW. J. H. Kappen has received grants or research support for consultations and/or speaking at conferences from ALK, Chiesi, GSK, Novartis, ASIT, AstraZeneca, Sanofi, Boehringer, Teva, Viatris, and Stallergen. The rest of the authors declare that they have no relevant conflicts of interest.
Funding Information:
This work was supported by The Netherlands Organisation for Health Research and Development (Zorgonderzoek Nederland en Medische Wetenschappen; ZonMW).
Publisher Copyright:
© 2026 The Authors
PY - 2026/7
Y1 - 2026/7
N2 - Background: Biologics in severe asthma are an effective but costly treatment. A personalized dosing strategy could reduce treatment burden and improve cost-effectiveness. Objective: To explore physician attitudes and real-world practices regarding dosing interval extensions for biologics in severe asthma. Methods: We assessed attitudes to dosing interval extension among Dutch pulmonologists prescribing biologics through a 28-item nationwide e-survey and investigated clinical practices using data from the Dutch severe asthma registry RAPSODI (Dutch Registry of Adult Patients with Severe asthma for Optimal DIsease management). Results: Of 50 pulmonologists, 39 (78%) reported extending dosing intervals, primarily due to good clinical response (95%) and treatment costs (77%). Most required at least 1 year of stable asthma (82%), which respondents defined as 6-item Asthma Control Questionnaire score less than 1.5, stable lung function, absence of exacerbations, and no maintenance oral corticosteroids. Reported success rates exceeded 50% for 62% of respondents, with failures mainly due to exacerbations or worsening symptoms. Interval extension was more frequent among physicians treating more than 25 patients with severe asthma (P < .01). Major barriers included lack of evidence (63%) and experience (52%), yet 91% expressed a wish to extend intervals more often. In RAPSODI (n = 1603), 159 interval extensions were recorded in 138 patients across 14 hospitals. Median increase in interval relative to the standard interval was 50% (range, 12.5%-300%) with multiple sequential extensions in 14% of patients. In 2024, the annual incidence of extensions was 5.2%, and the prevalence was 11.4%. Conclusions: A vast majority of Dutch pulmonologists already apply dosing interval extension of biologics in severe asthma, however on a limited scale. Although the frequency is increasing, clinicians are reluctant to apply extension broadly due to limited experience and evidence, highlighting the need for evidence-based guidelines.
AB - Background: Biologics in severe asthma are an effective but costly treatment. A personalized dosing strategy could reduce treatment burden and improve cost-effectiveness. Objective: To explore physician attitudes and real-world practices regarding dosing interval extensions for biologics in severe asthma. Methods: We assessed attitudes to dosing interval extension among Dutch pulmonologists prescribing biologics through a 28-item nationwide e-survey and investigated clinical practices using data from the Dutch severe asthma registry RAPSODI (Dutch Registry of Adult Patients with Severe asthma for Optimal DIsease management). Results: Of 50 pulmonologists, 39 (78%) reported extending dosing intervals, primarily due to good clinical response (95%) and treatment costs (77%). Most required at least 1 year of stable asthma (82%), which respondents defined as 6-item Asthma Control Questionnaire score less than 1.5, stable lung function, absence of exacerbations, and no maintenance oral corticosteroids. Reported success rates exceeded 50% for 62% of respondents, with failures mainly due to exacerbations or worsening symptoms. Interval extension was more frequent among physicians treating more than 25 patients with severe asthma (P < .01). Major barriers included lack of evidence (63%) and experience (52%), yet 91% expressed a wish to extend intervals more often. In RAPSODI (n = 1603), 159 interval extensions were recorded in 138 patients across 14 hospitals. Median increase in interval relative to the standard interval was 50% (range, 12.5%-300%) with multiple sequential extensions in 14% of patients. In 2024, the annual incidence of extensions was 5.2%, and the prevalence was 11.4%. Conclusions: A vast majority of Dutch pulmonologists already apply dosing interval extension of biologics in severe asthma, however on a limited scale. Although the frequency is increasing, clinicians are reluctant to apply extension broadly due to limited experience and evidence, highlighting the need for evidence-based guidelines.
KW - Biologics
KW - Dosing interval extension
KW - Personalized dosing
KW - Real-world practice
KW - Severe asthma
U2 - 10.1016/j.jaip.2026.03.029
DO - 10.1016/j.jaip.2026.03.029
M3 - Article
SN - 2213-2198
VL - 14
SP - 1612-1619.e3
JO - Journal of Allergy and Clinical Immunology: In Practice
JF - Journal of Allergy and Clinical Immunology: In Practice
IS - 7
ER -