4.4 Article

IL-23/Th17 targeted therapies in SAPHO syndrome. A case series

Journal

JOINT BONE SPINE
Volume 84, Issue 6, Pages 733-735

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.jbspin.2017.05.016

Keywords

SAPHO syndrome; IL-23; IL-17; Treatment; Ustekinumab; Secukinumab

Categories

Funding

  1. AbbVie
  2. BMS
  3. MSD
  4. Pfizer
  5. Roche Chugai
  6. Amgen
  7. Nordic Pharma
  8. UCB
  9. SOBI
  10. Sanofi Aventis
  11. Novartis
  12. Janssen
  13. Celgene
  14. Hospira
  15. Sandoz
  16. Lilly
  17. Roche
  18. Eli Lilly
  19. Medac

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SAPHO syndrome is a rare entity with skin and rheumatologic inflammatory presentation. The treatment is not standardized, and in case of inadequate response to anti-inflammatory drugs, the use of anti-TNF or anti-IL-1 biologic treatments has been reported. The IL-23/Th1 7 axis may be involved in SAPHO syndrome. We report the results of six courses of IL-23 and IL-17 targeted therapies (3 ustekinumab and 3 secukinumab) in patients with SAPHO syndrome unresponsive to previous treatments (csDMARDs and bDMARDs). With a mean treatment duration of 5.5 months, improvement of skin symptoms was noticed in three cases, one improvement with secukinumab and two remissions (one with secukinumab, one with ustekinumab). Regarding the rheumatic symptoms, no major improvement was obvious under any of the six treatment courses. No particular safety concerns were reported, except cases of paradoxical psoriasis flare in one under ustekinumab and the other case under secukinumab. (C) 2017 Societe francaise de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.

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