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Anti-IL-4R versus anti-IL-5/5R after anti-IL-5/5R failure in asthma: An emulated target trial.
Valery, Solène; Simon-Tillaux, Noémie; Devouassoux, Gilles; Bonniaud, Philippe; Beurnier, Antoine; Boudjemaa, Amel; Chenivesse, Cécile; Bourdin, Arnaud; Gauquelin, Lisa; Guillo, Sylvie; Taillé, Camille; Estellat, Candice.
Afiliação
  • Valery S; Service de Pneumologie et Centre de référence pour les maladies respiratoires rares, Hôpital Bichat, AP-HP Nord-Université Paris Cité, Paris, France; UMR 1152, Paris, France; CRISALIS F-CRIN Network, Toulouse, France; Sorbonne Université, INSERM, Institut Pierre Louis d'Épidémiologie et de Santé Pub
  • Simon-Tillaux N; Equipe 2-Oncostat U1018, Inserm, University Paris-Saclay, labeled Ligue Contre le Cancer, Department of Biostatistics and Epidemiology, Gustave Roussy, Villejuif, France.
  • Devouassoux G; CRISALIS F-CRIN Network, Toulouse, France; Service de Pneumologie, Hôpital de la Croix Rousse, Lyon, France.
  • Bonniaud P; CRISALIS F-CRIN Network, Toulouse, France; Service de Pneumologie et Soins Intensifs Respiratoire, Centre Hospitalier Universitaire de Bourgogne, Dijon, France; INSERM U1231, Equipe HSP-pathies, Faculty of Medicine and Pharmacy, University of Bourgogne-Franche Comté, Dijon, France.
  • Beurnier A; CRISALIS F-CRIN Network, Toulouse, France; Department of Respiratory and Intensive Care Medicine, AP-HP, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.
  • Boudjemaa A; Service de pneumologie, Centre Hospitalier intercommunal de Créteil, Créteil, France.
  • Chenivesse C; CRISALIS F-CRIN Network, Toulouse, France; Université de Lille, CNRS, Inserm, CHU Lille, Service de Pneumologie et Immuno-Allergologie, U1019 - UMR 9017- CIIL - Center for Infection and Immunity of Lille, Lille, France.
  • Bourdin A; CRISALIS F-CRIN Network, Toulouse, France; Department of Respiratory Diseases, University of Montpellier, Montpellier, France; PhyMedExp, University of Montpellier, CNRS, INSERM CHU Montpellier, Montpellier, France.
  • Gauquelin L; Sorbonne Université, INSERM, Institut Pierre Louis d'Épidémiologie et de Santé Publique, équipe PEPITES, AP-HP, Hôpital Pitié-Salpêtrière, Département de Santé Publique, Centre de Pharmacoépidémiologie (Cephepi), Paris, France.
  • Guillo S; Sorbonne Université, INSERM, Institut Pierre Louis d'Épidémiologie et de Santé Publique, équipe PEPITES, AP-HP, Hôpital Pitié-Salpêtrière, Département de Santé Publique, Centre de Pharmacoépidémiologie (Cephepi), Paris, France.
  • Taillé C; Service de Pneumologie et Centre de référence pour les maladies respiratoires rares, Hôpital Bichat, AP-HP Nord-Université Paris Cité, Paris, France; UMR 1152, Paris, France; CRISALIS F-CRIN Network, Toulouse, France.
  • Estellat C; Sorbonne Université, INSERM, Institut Pierre Louis d'Épidémiologie et de Santé Publique, équipe PEPITES, AP-HP, Hôpital Pitié-Salpêtrière, Département de Santé Publique, Centre de Pharmacoépidémiologie (Cephepi), Paris, France. Electronic address: candice.estellat@aphp.fr.
Article em En | MEDLINE | ID: mdl-38848878
ABSTRACT

BACKGROUND:

Switching biologics is now common practice in severe eosinophilic asthma. After insufficient response to anti-IL-5 or 5 receptor (anti-IL-5/5R), the optimal switch between an anti-IL-4R mAb (interclass) or another anti-IL-5/5R drug (intraclass) remains unknown.

OBJECTIVE:

We sought to compare the effectiveness of these 2 strategies in asthma control in patients with severe eosinophilic asthma and insufficient response to an anti-IL-5/5R mAb.

METHODS:

We emulated a target randomized trial using observational data from the Recherche sur les AsthMes SEvèreS (RAMSES) cohort. Eligible patients were switched to an anti-IL-4R mAb or another anti-IL-5/5R drug after insufficient response to an anti-IL-5/5R mAb. The primary outcome was the change in Asthma Control Test score at 6 months.

RESULTS:

Among the 2046 patients in the cohort, 151 were included in the study 103 switched to an anti-IL-4R mAb and 48 to another anti-IL-5/5R. At 6 months, the difference in Asthma Control Test score improvement was not statistically significant (mean difference groups, 0.82 [-0.47 to 2.10], P = .213). The interclass group exhibited greater cumulative reduction in oral corticosteroid dose (Pinter-intra, -1.05 g [-1.76 to -0.34], P = .041). The interclass group had a better effect, although not significantly, on reducing exacerbations (Δinter-intra, -0.37 [-0.77 to 0.02], P = .124) and increasing lung function (FEV1) (126.8 mL [-12.7 to 266.4], P = .124).

CONCLUSIONS:

After anti-IL-5/5R mAb insufficient response, switching to dupilumab demonstrated similar improvement in Asthma Control Test scores compared with intraclass switching. However, it appeared more effective in reducing oral corticosteroid use. Larger studies are warranted to confirm these results.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2024 Tipo de documento: Article