Abstract
Abstract
Introduction
Treat-to-target (T2T) strategies aim to facilitate tight disease control to improve outcomes. No previous studies evaluated prospectively the feasibility and impact of the T2T strategy in routine practice in childhood-onset SLE (cSLE).
Methods
Adolescents and young adults (AYA) with cSLE were recruited for T2T implementation from a large tertiary centre over a period of 6 months and followed up at least twice over a prospective period of 12 months.
Results
During Oct 2022–April 2023, 135/162 (83.3%) AYA with cSLE had disease scores evaluated at their routine appointment to enable inclusion in the study, and 122/135 (91.2%) had their disease assessed, and a suitable treatment target agreed and documented at each routine clinical appointment over the 12 months prospective follow-up. T2T strategy led to improved disease control at 12 months: more AYA with cSLE achieved clinical remission off steroids (4.1% vs. 10.7%, P = 0.048), or minimum childhood-lupus low disease activity (cLLDAS) (81.9% vs. 91.8%, P = 0.022). Achieving minimum cLLDAS for longer than 3 months was associated with reduced damage accrual (HR = 1.7; 95%CI = 1.1–2.5; P < 0.0001) at 12 months.
Conclusion
T2T strategy implementation was achievable and associated with improved cSLE control. Spending at least 3/12 months in cLLDAS led to less damage accumulation.
Key Points
• This is the first large prospective study in AYA with cSLE to evaluate the impact of active T2T implementation in routine practice.• T2T strategies were feasible to implement in 122/135 (91.2%) AYA with cSLE in routine practice.• The T2T approach was associated with improved disease control and decreased damage accrual at 12 months.
Funder
UCLH Biomedical Research Centre
Publisher
Springer Science and Business Media LLC
Reference31 articles.
1. Lisnevskaia L, Murphy G, Isenberg D (2014) Systemic lupus erythematosus. Lancet 384(9957):1878–1888
2. Massias JS, Smith EMD, Al-Abadi E, Armon K, Bailey K, Ciurtin C et al (2020) Clinical and laboratory characteristics in juvenile-onset systemic lupus erythematosus across age groups. Lupus 29(5):474–481
3. Ambrose N, Morgan TA, Galloway J, Ionnoau Y, Beresford MW, Isenberg DA, Group UJS (2016) Differences in disease phenotype and severity in SLE across age groups. Lupus. 25(14):1542–50
4. Lewis MJ, Jawad AS (2017) The effect of ethnicity and genetic ancestry on the epidemiology, clinical features and outcome of systemic lupus erythematosus. Rheumatology (Oxford). 56(suppl_1):i67–i77
5. Giani T, Smith EM, Al-Abadi E, Armon K, Bailey K, Ciurtin C et al (2021) Neuropsychiatric involvement in juvenile-onset systemic lupus erythematosus: data from the UK Juvenile-onset systemic lupus erythematosus cohort study. Lupus 30(12):1955–1965