Autoinflammatory & rare systemic diseases

Tocilizumab discontinuation after remission achievement in patients with adult-onset Still’s disease

Rheumatology (Oxford)Published Retrospective cohort study

Authors' conclusion

The recurrence rate after tocilizumab discontinuation was 50% in 1 year. Patients who remained in remission with a longer interval of tocilizumab administration and lower prednisolone dose were likely to succeed in the withdrawal of tocilizumab.

Study context

Population
Consecutive patients with adult-onset Still's disease (AOSD) (Yamaguchi's criteria), April 2012 to July 2022, treated with IV tocilizumab12 discontinued in remission
Participants
48 patients
Exposure
Non-recurrence vs recurrence after tocilizumab discontinuation in remission
  • Recurrencen = 6
  • Non-recurrencen = 6reference
Outcome
Recurrence after tocilizumab discontinuation during remission
Follow-up
1 year
Methodological detailsconsecutive patients
  • Consecutive patients

Main finding

As reported in the abstract

Recurrence after tocilizumab discontinuation

Recurrence within 1 year, at a mean of 5.5 months

6

50.0%

Remained in remission

6

50.0%

Observational data: associations, not effects.

Further findings

Interval of tocilizumab administration at discontinuation · tended to be shorter in recurrence

P = 0.08

Disease activity at tocilizumab discontinuation · no difference
systemic feature score, P = 0.24
Disease activity at tocilizumab discontinuation · no difference
ferritin, P = 0.46
Duration of tocilizumab use · not different
P = 0.32
Recurrence by prednisolone dose <7 mg/day at last tocilizumab treatment · Prednisolone <7 mg/day vs Prednisolone ≥7 mg/day · fewer recurrences with <7 mg/day
P = 0.001

Remission after 6 months of tocilizumab

Achieved remission
38 (79.2%)

Tocilizumab resumption after recurrence

Resumed in half of the patients, resulting in successful disease control

Original publication

Tocilizumab discontinuation after remission achievement in patients with adult-onset Still’s disease. Rheumatology (Oxford). Published 20 March 2024. doi:10.1093/rheumatology/keae179

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