Spondyloarthritis & psoriatic arthritis

Retention rate and predictors of discontinuation for secukinumab treatment: real-life data in a cohort of patients with spondyloarthritis

Clin Exp RheumatolPublished Retrospective cohort study

Authors' conclusion

Secukinumab demonstrates sustained effectiveness in SpA patients, with a significant proportion maintaining therapy over time. Retention is influenced by BMI, prior treatments, and disease phenotype

Study context

Population
Patients with spondyloarthritis (SpA) treated with secukinumab at a referral centre64.6% female
Participants
178 patients
Outcome
Secukinumab drug retention rate (time-to-discontinuation) and baseline predictors of discontinuation
Follow-up
12 months and end of study
Methodological detailsobservational, single referral centre, Cox proportional hazards regression
  • Observational
  • Single referral centre
  • Cox proportional hazards regression

Main finding

As reported in the abstract

Drug retention rate
GroupValueOverall drug retention rate (DRR)Retention at 1 year
Secukinumab64%64%78%

Secukinumab

Value64%
Overall drug retention rate (DRR)64%
Retention at 1 year78%

Observational data: associations, not effects.

Further findings

Predictors of long-term discontinuation · end of study

HR (95% CI)P value
Higher BMI1.07 (1.02–1.12)P = 0.010
Previous treatments1.34 (1.03–1.73)P = 0.030

Predictors of 12-month discontinuation

HR (95% CI)P value
Peripheral phenotype4.28 (1.26–14.48)P = 0.019
Prior biologic/targeted synthetic therapies1.76 (1.24–2.51)P = 0.002
Axial involvementProtective0.37 (0.17–0.83)P = 0.016

Reasons for discontinuation

Secondary inefficacy
57.8%
Primary inefficacy
25%

Safety

Discontinuation due to adverse events (proportion of discontinuations)

Adverse events as discontinuation reason
17.2%
Infections the most common adverse event

Original publication

Retention rate and predictors of discontinuation for secukinumab treatment: real-life data in a cohort of patients with spondyloarthritis. Clin Exp Rheumatol. Published 14 November 2024. doi:10.55563/clinexprheumatol/cruuvo

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