Lupus & antiphospholipid syndrome

Anifrolumab in systemic lupus erythematosus: real-world experience from a single academic tertiary care centre

Clin Exp RheumatolPublished Prospective observational cohort study

Authors' conclusion

In our real-world experience, anifrolumab achieved sustained remission after just 3 months of treatment and a significant reduction in disease activity in most patients.

Study context

Population
Systemic lupus erythematosus (SLE) patients starting anifrolumab per current guidelines (EULAR 2024), German academic tertiary care centre
Participants
26 patients
Exposure
Anifrolumab treatment: baseline vs follow-up
  • Anifrolumabn = 26
Outcome
Disease activity (SLEDAI-2K), baseline vs 3 months, mean ± SD
Follow-up
3 months
Methodological detailssingle-centre, real-world
  • Single-centre
  • Real-world

Main finding

As reported in the abstract

Baseline

6.0

SD 3.9

3 months

2.8

SD 2.6

P ≤ 0.001

Observational data: associations, not effects.

Further findings

Mucocutaneous manifestations, fatigue, arthritis/arthralgia

Mucocutaneous manifestations responded quickly; significant improvements in fatigue and arthritis/arthralgia

Response by prior therapies or disease duration

Favourable response also in patients with previous therapies or long disease duration

GC dose

Reduction in GC dose

Safety

Safety and tolerability

Overall, safe and well tolerated

Original publication

Anifrolumab in systemic lupus erythematosus: real-world experience from a single academic tertiary care centre. Clin Exp Rheumatol. Published 15 March 2025. doi:10.55563/clinexprheumatol/728zl6

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