Drug maintenance of a second tumor necrosis factor alpha inhibitor in spondyloarthritis patients: A real-life multicenter study.

Joint Bone Spine

Rheumatology Unit, Orleans hospital, 14, avenue de l'hôpital, CS86709, 45067 Orleans cedex, France; I3MTO Laboratory EA 4708, University Orleans, 45067 Orleans, France. Electronic address:

Published: November 2019

AI Article Synopsis

  • The study examined the survival rates of a second TNF inhibitor (TNFi) in patients with spondyloarthritis (SpA), noting that many patients stop their first TNFi within two years, but there are no clear guidelines for choosing a second one.
  • 244 SpA patients were followed over several years, revealing that the average duration for the first TNFi was significantly longer than for the second (21.7 months vs. 15.4 months), and switching between different types of TNFi did not impact drug survival.
  • Factors linked to better retention of the second TNFi included being male and being diagnosed with SpA at an age younger than 41, with age remaining a significant factor

Article Abstract

Objectives: Five TNF inhibitor (TNFi) agents are marketed for spondyloarthritis (SpA): 1 soluble receptor (SR) and 4 monoclonal antibodies (mAbs). From 15% to 30% of patients stop the first TNFi in the first 2 years, but we lack recommendations on the choice of the second TNFi. The aim here was to assess drug survival of a second TNFi in SpA and its determinants.

Methods: This was a multicenter observational study of SpA patients who started a first TNFi in 2013 and 2014 and were followed to 2018. For the first and second TNFi, we retrospectively collected data on initiation and discontinuation dates, type of TNFi, and reasons for withdrawal. Kaplan-Meier plots and log-rank tests were used to compare drug survival. Factors associated with drug survival of the second TNFi were analyzed by univariate Cox regression analyses.

Results: We included 244 patients. During a follow-up of 7,838 patient-months, 101 (41%) received 1 TNFi, and 143 (59%) switched to a second TNFi. Mean drug intake duration was significantly greater with the first than second TNFi: 21.7 (SD 19.6) and 15.4 (SD 13.6) months (P<0.001). When switching to another mAb or from an SR to an mAb (or the reverse), mean drug survival did not differ: 14.4 (SD 12.7) and 16 (SD 14.1) months (P=0.35). Factors associated with retaining the second TNFi were male sex (P=0.054) and age<41 years at SpA diagnosis (P=0.022). On multivariable analysis, only age<41 years at diagnosis remained independently associated with maintenance of the second TNFi.

Conclusion: In SpA patients, drug survival is significantly longer with the first than second TNFi. Male sex and age<41 years at diagnosis were associated with retaining the second TNFi.

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http://dx.doi.org/10.1016/j.jbspin.2019.07.003DOI Listing

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