Evolving Concepts in Treat-to-Target Strategies for Systemic Lupus Erythematosus Show others and affiliations
2024 (English) In: Mediterranean journal of rheumatology, E-ISSN 2529-198X, Vol. 35, no Suppl 2, p. 328-341Article, review/survey (Refereed) Published
Abstract [en]
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease that is characterised by a wide range of symptoms and a risk for irreversible organ damage, leading to increased morbidity and mortality. To improve long-term outcomes, innovative therapeutic goals have been explored, including attainment and maintenance of remission or low disease activity, with minimal use of glucocorticoids. Other goals encompass early diagnosis, potent yet less toxic therapies, appropriate glucocorticoid tapering, and better quality of life for the patients. Implementing a treat-to-target (T2T) approach involves treatment adjustments to achieve predefined objectives. Evidence from other chronic diseases, like hypertension and diabetes, supports the success of target-based approaches. In rheumatic diseases, the multitude of clinical features adds complexity to T2T strategies, but in rheumatoid arthritis, T2T has yielded improved outcomes. The application of T2T in SLE requires realistic therapeutic goals and practical tools for their measurement. International task forces have developed T2T recommendations for SLE, focusing on limiting disease activity, preventing organ damage, and minimising glucocorticoid use, while considering patients' quality of life. Advancements in defining clinically meaningful remission and low disease activity states, coupled with promising novel therapies, have spurred progress in the management of SLE.
Place, publisher, year, edition, pages Greek Rheumatology Society and Professional Association of Rheumatologists , 2024. Vol. 35, no Suppl 2, p. 328-341
Keywords [en]
Glucocorticoids, low disease activity, remission, systemic lupus erythematosus, treat-to-target
National Category
Clinical Medicine
Identifiers URN: urn:nbn:se:oru:diva-115691 DOI: 10.31138/mjr.290424.eci ISI: 001378265200002 PubMedID: 39193182 Scopus ID: 2-s2.0-85203048183 OAI: oai:DiVA.org:oru-115691 DiVA, id: diva2:1893573
Funder Swedish Rheumatism Association, R-969696; R-995557 Stiftelsen Konung Gustaf V:s 80-årsfond, FAI-2020-0741 Swedish Society of Medicine, SLS-974449 Nyckelfonden, OLL-974804 Region Stockholm, FoUI-955483 Karolinska Institute
Note IP has received grants from the Swedish Rheumatism Association (R-969696), King Gustaf V's 80-year Foundation (FAI-2020-0741), Swedish Society of Medicine (SLS-974449), Nyckelfonden (OLL-974804), Professor Nanna Svartz Foundation (2021-00436), Ulla and Roland Gustafsson Foundation (2021-26), Region Stockholm (FoUI-955483), and Karolinska Institutet. DN has received grants from Ulla o Roland Gustafssons Donationsfond (2024-49), Ulla och Gustaf af Ugglas stiftelse (2023-025029) and Reumatikerforbundet (2024 R-995557).
2024-08-292024-08-292025-02-18 Bibliographically approved