[Discontinuation or tapering strategies of biologics in rheumatoid arthritis in remission]

Rev Med Interne. 2017 Apr;38(4):256-263. doi: 10.1016/j.revmed.2016.12.014. Epub 2017 Feb 1.
[Article in French]

Abstract

The arrival of new drugs and new therapeutic strategies allowed to reach sustained remission in an increasing number of patients with rheumatoid arthritis. The study of biologic disease-modifying anti-rheumatic drugs (bDMARDs) adaptation strategies is a need to optimize the benefit/risk balance and cost/effectiveness ratio of these molecules. Current recommendations such as EULAR 2016 propose tapering bDMARDs, especially when combined with a csDMARD, when the patient is in remission after stopping persistent glucocorticoids. The analysis of literature comprising 22 studies shows that a bDMARD adaptation is possible in established rheumatoid arthritis when clinico-biological and ultrasound remission is maintained over six months. Priority should be given to a progressive tapering strategy doses controlled by disease activity while maintaining "tight control" to identify and effectively treat a relapse, a retreatment being usually favorable.

Keywords: Dose reduction; Décroissance du traitement; Espacement; Polyarthrite rhumatoïde; Remission; Rheumatoid arthritis; Réduction de dose; Rémission; Spacing; Treatment tapering.

Publication types

  • Review

MeSH terms

  • Antirheumatic Agents / administration & dosage*
  • Arthritis, Rheumatoid / drug therapy*
  • Biological Factors / administration & dosage
  • Biological Products / administration & dosage*
  • Dose-Response Relationship, Drug
  • Humans
  • Practice Patterns, Physicians'
  • Recurrence
  • Remission Induction
  • Withholding Treatment* / standards

Substances

  • Antirheumatic Agents
  • Biological Factors
  • Biological Products