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High discontinuation rate of azathioprine in autoimmune hepatitis, independent of time of treatment initiation

  • Simon Pape*
  • , Tom J. G. Gevers
  • , Jan Maarten Vrolijk
  • , Bart van Hoek
  • , Gerd Bouma
  • , Carin M. J. van Nieuwkerk
  • , Richard Taubert
  • , Elmar Jaeckel
  • , Michael P. Manns
  • , Maria Papp
  • , Nora Sipeki
  • , Felix Stickel
  • , Cumali Efe
  • , Ersan Ozaslan
  • , Tugrul Purnak
  • , Frederik Nevens
  • , Dominik J. N. Kessener
  • , Alisan Kahraman
  • , Heiner Wedemeyer
  • , Johannes Hartl
  • Christoph Schramm, Ansgar W. Lohse, Michael A. Heneghan, Joost P. H. Drenth
*Corresponding author for this work
  • Radboud University Medical Center
  • European Reference Network on Hepatological Diseases (ERN RARE-LIVER)
  • Rijnstate Hospital
  • Leiden University Medical Center
  • Amsterdam UMC - Vrije Universiteit Amsterdam
  • Hannover Medical School
  • University of Debrecen
  • University Hospital Zürich
  • Harran University
  • Hacettepe University
  • KU Leuven
  • University of Duisburg-Essen
  • University of Hamburg
  • King's College Hospital, London
  • Radboud University Nijmegen
  • European Reference Network RARE-LIVER
  • Leiden University
  • University of Zurich
  • Ankara Numune Education and Research Hospital
  • King's College Hospital NHS Foundation Trust

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Background: Guidelines regarding treatment for autoimmune hepatitis (AIH) favour two strategies for azathioprine (AZA) introduction: concurrent with steroids at induction or delayed by 2-4 weeks. The safety and efficacy of both strategies have been unexplored. Methods: We established a cohort of 900 AIH patients from 12 centres in 7 European countries. There were 631 patients who used AZA as part of the therapeutic regimen. We distinguished two groups: patients with early AZA (<2 weeks) or delayed AZA initiation (≥2 weeks). Primary outcome was discontinuation of AZA in the first year of treatment. Cox regression and propensity score matching was performed to determine difference in outcomes between groups. Results: Patients with early AZA initiation had significantly lower transaminases and bilirubin at baseline. Discontinuation rates of AZA did not differ between early and delayed starters (16.6% vs 14.2%), which did not reach statistical significance (hazard ratio 0.97, 95% confidence interval 0.61-1.55, P =.90). Stratification according to baseline disease activity or propensity score matching did not alter the results. Main reason for AZA discontinuation was intolerance to treatment (14.0% vs 13.2%, P =.78) with nausea and vomiting as main side effects. AIH remission rates were comparable among groups. Conclusion: The discontinuation rate of AZA in AIH treatment is ~15% in the first year of treatment. Early or delayed AZA initiation does not differ in remission and discontinuation rates in AIH induction therapy. Our data suggest that either strategy may be used as part of AIH treatment.
Original languageEnglish
Pages (from-to)2164-2171
Number of pages8
JournalLiver international
Volume40
Issue number9
DOIs
Publication statusPublished - 1 Sept 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • autoimmune hepatitis
  • azathioprine
  • cohort study
  • immunosupression

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