Real-life impact of immunologic tests to predict relapse after treatment cessation in patients with bullous pemphigoid: A French multicenter retrospective study

J Am Acad Dermatol. 2022 Jun;86(6):1293-1300. doi: 10.1016/j.jaad.2022.01.016. Epub 2022 Jan 26.

Abstract

Background: A high level of anti-BP180 antibodies on enzyme-linked immunosorbent assay and a persistent positive direct immunofluorescence at the end of treatment (immunologic tests, [ITs]) are predictors of relapse after treatment cessation (TC) in patients with bullous pemphigoid.

Objective: To evaluate the real-life impact of the immunologic-based decision of TC on the 3- and 6-month relapse rates after TC in bullous pemphigoid.

Methods: Retrospective multicentric study included patients followed almost 6 months after TC. Patients were classified according to whether the TC decision was in accordance with the results of ITs performed during the 3 months before TC, despite the results of ITs or without ITs performed.

Results: We included 238 patients. Three months after TC, 36 patients showed relapse: 14 of 95 patients with TC in accordance with IT results (14.7%); 5 of 21 with TC despite ITs (23.8%); and 17 of 122 with TC without ITs (13.9%; P = .5). Six months after TC, the relapse rate was 18.9%, 28.6%, and 18.9% (P = .56), respectively, in the 3 groups.

Limitations: The retrospective design and the limited follow up.

Conclusion: In real-life practice, in bullous pemphigoid, the 3- and 6-month relapse rates were not significantly reduced with TC decision based on results of ITs as compared with a classic clinical-based decision.

Keywords: DIF; ELISA; anti-BP180; bullous pemphigoid; relapse; treatment cessation.

Publication types

  • Multicenter Study

MeSH terms

  • Autoantibodies
  • Autoantigens
  • Enzyme-Linked Immunosorbent Assay / methods
  • Humans
  • Immunologic Tests
  • Non-Fibrillar Collagens
  • Pemphigoid, Bullous* / drug therapy
  • Recurrence
  • Retrospective Studies
  • Withholding Treatment

Substances

  • Autoantibodies
  • Autoantigens
  • Non-Fibrillar Collagens