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Incidence and risk factors for adalimumab and infliximab anti-drug antibodies in rheumatoid arthritis: A European retrospective multicohort analysis.
Quistrebert, Jocelyn; Hässler, Signe; Bachelet, Delphine; Mbogning, Cyprien; Musters, Anne; Tak, Paul Peter; Wijbrandts, Carla Ann; Herenius, Marieke; Bergstra, Sytske Anne; Akdemir, Gülsah; Johannesson, Martina; Combe, Bernard; Fautrel, Bruno; Chollet-Martin, Sylvie; Gleizes, Aude; Donnellan, Naoimh; Deisenhammer, Florian; Davidson, Julie; Hincelin-Mery, Agnès; Dönnes, Pierre; Fogdell-Hahn, Anna; De Vries, Niek; Huizinga, Tom; Abugessaisa, Imad; Saevarsdottir, Saedis; Hacein-Bey-Abina, Salima; Pallardy, Marc; Broët, Philippe; Mariette, Xavier.
Afiliação
  • Quistrebert J; CESP, INSERM UMR 1018, Faculty of Medicine, Paris-Sud University, Paris-Saclay University, UVSQ, Villejuif, France.
  • Hässler S; CESP, INSERM UMR 1018, Faculty of Medicine, Paris-Sud University, Paris-Saclay University, UVSQ, Villejuif, France.
  • Bachelet D; CESP, INSERM UMR 1018, Faculty of Medicine, Paris-Sud University, Paris-Saclay University, UVSQ, Villejuif, France.
  • Mbogning C; CESP, INSERM UMR 1018, Faculty of Medicine, Paris-Sud University, Paris-Saclay University, UVSQ, Villejuif, France.
  • Musters A; Amsterdam Rheumatology and Immunology Center, Academic Medical Center of the University of Amsterdam, Amsterdam, the Netherlands.
  • Tak PP; Amsterdam Rheumatology and Immunology Center, Academic Medical Center of the University of Amsterdam, Amsterdam, the Netherlands; GlaxoSmithKline, Stevenage, UK; University of Cambridge, Cambridge, UK; Ghent University, Ghent, Belgium.
  • Wijbrandts CA; Amsterdam Rheumatology and Immunology Center, Academic Medical Center of the University of Amsterdam, Amsterdam, the Netherlands; Medical Center Slotervaart, Amsterdam, the Netherlands.
  • Herenius M; Amsterdam Rheumatology and Immunology Center, Academic Medical Center of the University of Amsterdam, Amsterdam, the Netherlands.
  • Bergstra SA; Department of Rheumatology, Leiden University Medical Center, Leiden, the Netherlands.
  • Akdemir G; Department of Rheumatology, Leiden University Medical Center, Leiden, the Netherlands.
  • Johannesson M; Rheumatology Unit, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Combe B; Department of Rheumatology, Lapeyronie Hospital, Montpellier University, Montpellier, France.
  • Fautrel B; Department of Rheumatology, AP-HP, Pitié Salpétrière Hospital, Paris, France; UPMC, GRC 08, Pierre Louis Institute of Epidemiology and Public Health, Paris, France.
  • Chollet-Martin S; INSERM UMR 996, Faculty of Pharmacy, Paris-Sud University, Paris-Saclay University, Châtenay-Malabry, France.
  • Gleizes A; INSERM UMR 996, Faculty of Pharmacy, Paris-Sud University, Paris-Saclay University, Châtenay-Malabry, France; Clinical Immunology Laboratory, AP-HP, Paris-Sud University Hospitals, Le Kremlin Bicêtre Hospital, Le Kremlin Bicêtre, France.
  • Donnellan N; IPSEN, Slough, Berkshire, UK.
  • Deisenhammer F; Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.
  • Davidson J; GlaxoSmithKline, Uxbridge, Middlesex, UK.
  • Hincelin-Mery A; Sanofi, Chilly-Mazarin, France.
  • Dönnes P; SciCross AB, Skövde, Sweden.
  • Fogdell-Hahn A; Department of Clinical Neuroscience, Clinical Neuroimmunology, Karolinska Institutet, Stockholm, Sweden.
  • De Vries N; Amsterdam Rheumatology and Immunology Center, Academic Medical Center of the University of Amsterdam, Amsterdam, the Netherlands.
  • Huizinga T; Department of Rheumatology, Leiden University Medical Center, Leiden, the Netherlands.
  • Abugessaisa I; Unit of Computational Medicine, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
  • Saevarsdottir S; Rheumatology Unit, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Hacein-Bey-Abina S; Clinical Immunology Laboratory, AP-HP, Paris-Sud University Hospitals, Le Kremlin Bicêtre Hospital, Le Kremlin Bicêtre, France; UTCBS, CNRS UMR 8258, INSERM U1022, Faculty of Pharmacy, Paris-Descartes-Sorbonne-Cité University, Paris, France.
  • Pallardy M; INSERM UMR 996, Faculty of Pharmacy, Paris-Sud University, Paris-Saclay University, Châtenay-Malabry, France.
  • Broët P; CESP, INSERM UMR 1018, Faculty of Medicine, Paris-Sud University, Paris-Saclay University, UVSQ, Villejuif, France; AP-HP, Paris-Sud University Hospitals, Paul Brousse Hospital, Villejuif, France; CHU Sainte Justine, Quebec, Canada.
  • Mariette X; INSERM U1184, Center for Immunology of Viral Infections and Autoimmune Diseases, Paris-Sud University, Paris-Saclay University, Le Kremlin-Bicêtre, France; Department of Rheumatology, AP-HP, Paris-Sud University Hospitals, Le Kremlin Bicêtre Hospital, Le Kremlin-Bicêtre, France. Electronic address:
Semin Arthritis Rheum ; 48(6): 967-975, 2019 06.
Article em En | MEDLINE | ID: mdl-30420245
ABSTRACT

OBJECTIVES:

To evaluate the incidence of anti-drug antibody (ADA) occurrences and ADA-related risk factors under adalimumab and infliximab treatment in rheumatoid arthritis (RA) patients.

METHODS:

The study combined retrospective cohorts from the ABIRISK project totaling 366 RA patients treated with adalimumab (n = 240) or infliximab (n = 126), 92.4% of them anti-TNF naive (n = 328/355) and 96.6% of them co-treated with methotrexate (n = 341/353) with up to 18 months follow-up. ADA positivity was measured by enzyme-linked immunosorbent assay. The cumulative incidence of ADA was estimated, and potential bio-clinical factors were investigated using a Cox regression model on interval-censored data.

RESULTS:

ADAs were detected within 18 months in 19.2% (n = 46) of the adalimumab-treated patients and 29.4% (n = 37) of the infliximab-treated patients. The cumulative incidence of ADA increased over time. In the adalimumab and infliximab groups, respectively, the incidence was 15.4% (5.2-20.2) and 0% (0-5.9) at 3 months, 17.6% (11.4-26.4) and 0% (0-25.9) at 6 months, 17.7% (12.6-37.5) and 34.1% (11.4-46.3) at 12 months, 50.0% (25.9-87.5) and 37.5% (25.9-77.4) at 15 months and 50.0% (25.9-87.5) and 66.7% (37.7-100) at 18 months. Factors associated with a higher risk of ADA development were longer disease duration (1-3 vs. < 1 year; adalimumab HR 3.0, 95% CI 1.0-8.7; infliximab HR 2.7, 95% CI 1.1-6.8), moderate disease activity (DAS28 3.2-5.1 vs. < 3.2; adalimumab HR 6.6, 95% CI 1.3-33.7) and lifetime smoking (infliximab HR 2.7, 95% CI 1.2-6.3).

CONCLUSIONS:

The current study focusing on patients co-treated with methotrexate for more than 95% of them found a late occurrence of ADAs not previously observed, whereby the risk continued to increase over 18 months. Disease duration, DAS28 and lifetime smoking are clinical predictors of ADA development.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Antirreumáticos / Adalimumab / Infliximab / Anticorpos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Antirreumáticos / Adalimumab / Infliximab / Anticorpos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article