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Biomarker Predictors of Clinical Efficacy of the Anti-IgE Biologic, Omalizumab, in Severe Asthma in Adults: Results of the SoMOSA Study.
Djukanovic, Ratko; Brinkman, Paul; Kolmert, Johan; Gomez, Cristina; Schofield, James; Brandsma, Joost; Shapanis, Andy; Skipp, Paul J S; Postle, Anthony; Wheelock, Craig; Dahlén, Sven-Erik; Sterk, Peter J; Brown, Thomas; Jackson, David J; Mansur, Adel; Pavord, Ian; Patel, Mitesh; Brightling, Christopher; Siddiqui, Salman; Bradding, Peter; Sabroe, Ian; Saralaya, Dinesh; Chishimba, Livingstone; Porter, Joanna; Robinson, Douglas; Fowler, Stephen J; Howarth, Peter H; Little, Louisa; Oliver, Thomas; Hill, Kayleigh; Stanton, Louise; Allen, Alexander; Ellis, Deborah; Griffiths, Gareth; Harrison, Tim; Akenroye, Ayobami; Lasky-Su, Jessica; Heaney, Liam; Chaudhuri, Rekha; Kurukulaaratchy, Ramesh.
Afiliação
  • Djukanovic R; Southampton University, Clinical and Experimental Sciences and Southampton NIHR Respiratory Biomedical Research Unit, Southampton, United Kingdom of Great Britain and Northern Ireland; R.Djukanovic@soton.ac.uk.
  • Brinkman P; Amsterdam UMC - Locatie AMC, 26066, Pulmonary Medicine, Amsterdam, North Holland, Netherlands.
  • Kolmert J; Karolinska Institutet, Institute of Environmental Medicine, Stockholm, Sweden.
  • Gomez C; Karolinska Institutet Institute of Environmental Medicine, 193414, Stockholm, Sweden.
  • Schofield J; Centre for Allergy Research, Karolinska Institutet, Stockholm, Sweden.
  • Brandsma J; University of Southampton Centre for Biological Sciences, 98463, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Shapanis A; University of Southampton Faculty of Medicine, NIHR Southampton Biomedical Research Centre, CES, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Skipp PJS; Southampton University, Biological Sciences, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Postle A; University of Southampton Centre for Biological Sciences, 98463, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Wheelock C; University of Southampton, Clinical & Experimental Sciences, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Dahlén SE; Karolinska Institutet, 27106, Medical Biochemistry and Biophysics, Stockholm, Stockholm County, Sweden.
  • Sterk PJ; Karolinska Intitutet, Centre for Allergy Research, Stockholm, Sweden.
  • Brown T; University of Amsterdam, Academic Medical Center, Pulmonology, F5-259, Amsterdam, Netherlands.
  • Jackson DJ; Portsmouth Hospitals NHS Trust, Respiratory Medicine, Portsmouth, Hampshire, United Kingdom of Great Britain and Northern Ireland.
  • Mansur A; Guy's and St. Thomas' Hospitals, Guy's Severe Asthma Centre, London, United Kingdom of Great Britain and Northern Ireland.
  • Pavord I; Birmingham Heartlands Hospital, Respiratory Medicine, Birmingham, West Midlands, United Kingdom of Great Britain and Northern Ireland.
  • Patel M; Oxford University, Nuffield department of Medicine, Respiratory Medicine, Oxford, Oxfordshire, United Kingdom of Great Britain and Northern Ireland.
  • Brightling C; University Hospitals Plymouth NHS Trust, 6634, Respiratory Medicine and R&D, Plymouth, United Kingdom of Great Britain and Northern Ireland.
  • Siddiqui S; University of Leicester, Department of Infection, Immunity and Inflammation, Leicester, United Kingdom of Great Britain and Northern Ireland.
  • Bradding P; Imperial College London, 4615, National Heart and Lung Institute, London, United Kingdom of Great Britain and Northern Ireland.
  • Sabroe I; Leicester Institute for Lung Health, Department of Infection, Immunity and Inflammation, Leicester, United Kingdom of Great Britain and Northern Ireland.
  • Saralaya D; University of Sheffield, Division of Genomic Medicine, Sheffield, United Kingdom of Great Britain and Northern Ireland.
  • Chishimba L; Bradford Teaching Hospitals NHS Foundation Trust, 1906, Bradford, United Kingdom of Great Britain and Northern Ireland.
  • Porter J; Liverpool School of Tropical Medicine, 9655, Clinical Sciences, Liverpool, United Kingdom of Great Britain and Northern Ireland.
  • Robinson D; University College London, Centre for Inflammation and Tissue Repair, London, United Kingdom of Great Britain and Northern Ireland.
  • Fowler SJ; University College London, 4919, UCL Respiratory and NIHR University College London Hospitals Biomedical Research Centre, London, United Kingdom of Great Britain and Northern Ireland.
  • Howarth PH; University of Manchester, Respiratory Research Group, Manchester, United Kingdom of Great Britain and Northern Ireland.
  • Little L; University of Southampton, 7423, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Oliver T; Southampton University Hospitals NHS Trust, 7425, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Hill K; University of Southampton Faculty of Medicine, 12211, Southampton Clinical Trials Unit, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Stanton L; University of Southampton Faculty of Medicine, 12211, Southampton Clinical trials Unit, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Allen A; University of Southampton Faculty of Medicine, 12211, Southampton Clinical Trials Unit, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Ellis D; University of Southampton Faculty of Medicine, 12211, Southampton Clinical Trials Unit, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Griffiths G; University of Southampton Faculty of Medicine, 12211, Southampton Clinical Trials Unit, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Harrison T; University of Southampton Faculty of Medicine, 12211, Southampton Clinical Trials Unit, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Akenroye A; University of Nottingham, 6123, Division of Respiratory Medicine and Respiratory Research Unit, Nottingham, United Kingdom of Great Britain and Northern Ireland.
  • Lasky-Su J; Brigham and Women's Hospital, 1861, Medicine (Allergy & Clinical Immunology), Boston, Massachusetts, United States.
  • Heaney L; Brigham and Women's Hospital, Boston, Massachusetts, United States.
  • Chaudhuri R; Belfast City Hospital, Regional Respiratory Centre, Belfast, United Kingdom of Great Britain and Northern Ireland.
  • Kurukulaaratchy R; Gartnavel General Hospital, 59731, Glasgow, United Kingdom of Great Britain and Northern Ireland.
Article em En | MEDLINE | ID: mdl-38635834
ABSTRACT

BACKGROUND:

The anti-IgE monoclonal, omalizumab, is widely used for severe asthma. This study aimed to identify biomarkers that predict clinical improvement during one year of omalizumab treatment.

METHODS:

1-year, open-label, Study of Mechanisms of action of Omalizumab in Severe Asthma (SoMOSA) involving 216 severe (GINA step 4/5) uncontrolled atopic asthmatics (≥2 severe exacerbations in previous year) on high-dose inhaled corticosteroids, long-acting ß-agonists, ± mOCS. It had two phases 0-16 weeks, to assess early clinical improvement by Global Evaluation of Therapeutic Effectiveness (GETE), and 16-52 weeks, to assess late responses by ≥50% reduction in exacerbations or dose of maintenance oral corticosteroids (mOCS). All participants provided samples (exhaled breath, blood, sputum, urine) before and after 16 weeks of omalizumab treatment.

RESULTS:

191 patients completed phase 1; 63% had early improvement. Of 173 who completed phase 2, 69% had reduced exacerbations by ≥50%, while 57% (37/65) on mOCS reduced their dose by ≥50%. The primary outcome 2, 3-dinor-11-ß-PGF2α, GETE and standard clinical biomarkers (blood and sputum eosinophils, exhaled nitric oxide, serum IgE) did not predict either clinical response. Five breathomics (GC-MS) and 5 plasma lipid biomarkers strongly predicted the ≥50% reduction in exacerbations (receiver operating characteristic area under the curve (AUC) 0.780 and 0.922, respectively) and early responses (AUC0.835 and 0.949, respectively). In independent cohorts, the GC-MS biomarkers differentiated between severe and mild asthma. Conclusions This is the first discovery of omics biomarkers that predict improvement to a biologic for asthma. Their prospective validation and development for clinical use is justified. This article is open access and distributed under the terms of the Creative Commons Attribution 4.0 International License (https//creativecommons.org/licenses/by/4.0/).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Respir Crit Care Med Assunto da revista: TERAPIA INTENSIVA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Respir Crit Care Med Assunto da revista: TERAPIA INTENSIVA Ano de publicação: 2024 Tipo de documento: Article
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