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Association Between T2-related Comorbidities and Effectiveness of Biologics in Severe Asthma.
Wechsler, Michael E; Scelo, Ghislaine; Larenas-Linnemann, Désirée E S; Torres-Duque, Carlos A; Maspero, Jorge; Tran, Trung N; Murray, Ruth B; Martin, Neil; Menzies-Gow, Andrew N; Hew, Mark; Peters, Matthew J; Gibson, Peter G; Christoff, George C; Popov, Todor A; Côté, Andréanne; Bergeron, Celine; Dorscheid, Delbert; FitzGerald, J Mark; Chapman, Kenneth R; Boulet, Louis Philippe; Bhutani, Mohit; Sadatsafavi, Mohsen; Jiménez-Maldonado, Libardo; Duran-Silva, Mauricio; Rodriguez, Bellanid; Celis-Preciado, Carlos Andres; Cano-Rosales, Diana Jimena; Solarte, Ivan; Fernandez-Sanchez, Maria Jose; Parada-Tovar, Patricia; von Bülow, Anna; Bjerrum, Anne Sofie; Ulrik, Charlotte S; Assing, Karin Dahl; Rasmussen, Linda Makowska; Hansen, Susanne; Altraja, Alan; Bourdin, Arnaud; Taille, Camille; Charriot, Jeremy; Roche, Nicolas; Papaioannou, Andriana I; Kostikas, Konstantinos; Papadopoulos, Nikolaos G; Salvi, Sundeep; Long, Deirdre; Mitchell, Patrick D; Costello, Richard; Sirena, Concetta; Cardini, Cristina.
Afiliación
  • Wechsler ME; Cohen Family Asthma Institute and Department of Medicine.
  • Scelo G; Observational and Pragmatic Research Institute, Singapore.
  • Larenas-Linnemann DES; Optimum Patient Care Global, Cambridge, United Kingdom.
  • Torres-Duque CA; Centro de Excelencia en Asma y Alergia, Hospital Médica Sur, Ciudad de México, Mexico.
  • Maspero J; CINEUMO/Centro Internacional de Investigación en Neumología, Respiratory Research Center, Fundación Neumológica Colombiana, Bogotá, Colombia.
  • Tran TN; Universidad de La Sabana, Chia, Colombia.
  • Murray RB; Clinical Research for Allergy and Respiratory Medicine, CIDEA Foundation, Buenos Aires, Argentina.
  • Martin N; BioPharmaceuticals Medical, AstraZeneca, Gaithersburg, Maryland.
  • Menzies-Gow AN; Optimum Patient Care Global, Cambridge, United Kingdom.
  • Hew M; BioPharmaceuticals Medical, AstraZeneca, Gaithersburg, Maryland.
  • Peters MJ; University of Leicester, Leicester, United Kingdom.
  • Gibson PG; AstraZeneca, Cambridge, United Kingdom.
  • Christoff GC; Royal Brompton & Harefield Hospitals, London, United Kingdom.
  • Popov TA; Allergy, Asthma & Clinical Immunology Service, Alfred Health, Melbourne, Victoria, Australia.
  • Côté A; Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
  • Bergeron C; Department of Thoracic Medicine, Concord Hospital, Sydney, New South Wales, Australia.
  • Dorscheid D; Australian Severe Asthma Network, Priority Research Centre for Healthy Lungs, University of Newcastle, Newcastle, New South Wales, Australia.
  • FitzGerald JM; Hunter Medical Research Institute, Department of Respiratory and Sleep Medicine, John Hunter Hospital, New Lambton Heights, New South Wales, Australia.
  • Chapman KR; Medical University, Sofia, Bulgaria.
  • Boulet LP; University Hospital Sv. Ivan Rilski, Sofia, Bulgaria.
  • Bhutani M; Department of Medicine, Laval University, Quebec City, Quebec, Canada.
  • Sadatsafavi M; Vancouver General Hospital and University of British Columbia, Vancouver, British Columbia, Canada.
  • Jiménez-Maldonado L; Center for Heart Lung Innovation.
  • Duran-Silva M; Department of Medicine, and.
  • Rodriguez B; University of Toronto, Toronto, Ontario, Canada.
  • Celis-Preciado CA; Québec Heart and Lung Institute, Université Laval, Quebec City, Quebec, Canada.
  • Cano-Rosales DJ; Division of Pulmonary Medicine, Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.
  • Solarte I; Respiratory Evaluation Sciences Program, Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
  • Fernandez-Sanchez MJ; Fundación Neumológica Colombiana, Atención integral y rehabilitación en asma or Comprehensive Care and Rehabilitation in Asthma (ASMAIRE) Programa, Bogotá, Colombia.
  • Parada-Tovar P; Fundación Neumológica Colombiana, Atención integral y rehabilitación en asma or Comprehensive Care and Rehabilitation in Asthma (ASMAIRE) Programa, Bogotá, Colombia.
  • von Bülow A; Instituto Neumológico del Oriente, Bucaramanga, Colombia.
  • Bjerrum AS; Pulmonary Unit, San Ignacio University Hospital, Bogota, Colombia.
  • Ulrik CS; Faculty of Medicine, Pontificia University Javeriana, Bogota, Colombia.
  • Assing KD; Instituto Neumológico del Oriente, Bucaramanga, Colombia.
  • Rasmussen LM; Pulmonary Unit, San Ignacio University Hospital, Bogota, Colombia.
  • Hansen S; Faculty of Medicine, Pontificia University Javeriana, Bogota, Colombia.
  • Altraja A; Pulmonary Unit, San Ignacio University Hospital, Bogota, Colombia.
  • Bourdin A; Faculty of Medicine, Pontificia University Javeriana, Bogota, Colombia.
  • Taille C; CINEUMO/Centro Internacional de Investigación en Neumología, Respiratory Research Center, Fundación Neumológica Colombiana, Bogotá, Colombia.
  • Charriot J; Respiratory Research Unit, Department of Respiratory Medicine and Infectious Diseases, Bispebjerg Hospital, Copenhagen, Denmark.
  • Roche N; Department of Respiratory Medicine and Allergy, Aarhus University Hospital, Aarhus City, Denmark.
  • Papaioannou AI; Department of Respiratory Medicine, Copenhagen University, Hvidovre Hospital, Hvidovre, Denmark.
  • Kostikas K; Department of Respiratory Medicine, Aalborg University Hospital, Aalborg, Denmark.
  • Papadopoulos NG; Allergy Clinic, Copenhagen University Hospital-Gentofte, Hellerup, Denmark.
  • Salvi S; Respiratory Research Unit, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Long D; Center for Clinical Research and Prevention, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark.
  • Mitchell PD; Department of Pulmonology, University of Tartu and Lung Clinic, Tartu University Hospital, Tartu, Estonia.
  • Costello R; PhyMedExp, Université de Montpellier, Centre National de Recherche Scientifique, Institut National de la Santé et de la Recherche Médicale, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
  • Sirena C; Department of Respiratory Diseases, Bichat Hospital, Public Assistance-Hospitals of Paris North, Paris City University, Paris, France.
  • Cardini C; PhyMedExp, Université de Montpellier, Centre National de Recherche Scientifique, Institut National de la Santé et de la Recherche Médicale, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
Am J Respir Crit Care Med ; 209(3): 262-272, 2024 Feb 01.
Article en En | MEDLINE | ID: mdl-38016003
ABSTRACT
Rationale Previous studies investigating the impact of comorbidities on the effectiveness of biologic agents have been relatively small and of short duration and have not compared classes of biologic agents.

Objectives:

To determine the association between type 2-related comorbidities and biologic agent effectiveness in adults with severe asthma (SA).

Methods:

This cohort study used International Severe Asthma Registry data from 21 countries (2017-2022) to quantify changes in four outcomes before and after biologic therapy-annual asthma exacerbation rate, FEV1% predicted, asthma control, and long-term oral corticosteroid daily dose-in patients with or without allergic rhinitis, chronic rhinosinusitis (CRS) with or without nasal polyps (NPs), NPs, or eczema/atopic dermatitis. Measurements and Main

Results:

Of 1,765 patients, 1,257, 421, and 87 initiated anti-IL-5/5 receptor, anti-IgE, and anti-IL-4/13 therapies, respectively. In general, pre- versus post-biologic therapy improvements were noted in all four asthma outcomes assessed, irrespective of comorbidity status. However, patients with comorbid CRS with or without NPs experienced 23% fewer exacerbations per year (95% CI, 10-35%; P < 0.001) and had 59% higher odds of better post-biologic therapy asthma control (95% CI, 26-102%; P < 0.001) than those without CRS with or without NPs. Similar estimates were noted for those with comorbid NPs 22% fewer exacerbations and 56% higher odds of better post-biologic therapy control. Patients with SA and CRS with or without NPs had an additional FEV1% predicted improvement of 3.2% (95% CI, 1.0-5.3; P = 0.004), a trend that was also noted in those with comorbid NPs. The presence of allergic rhinitis or atopic dermatitis was not associated with post-biologic therapy effect for any outcome assessed.

Conclusions:

These findings highlight the importance of systematic comorbidity evaluation. The presence of CRS with or without NPs or NPs alone may be considered a predictor of the effectiveness of biologic agents in patients with SA.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Asma / Sinusitis / Productos Biológicos / Rinitis / Pólipos Nasales / Rinitis Alérgica Límite: Adult / Humans Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Asma / Sinusitis / Productos Biológicos / Rinitis / Pólipos Nasales / Rinitis Alérgica Límite: Adult / Humans Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2024 Tipo del documento: Article