TY - JOUR
T1 - 2025 American College of Rheumatology (ACR) Guideline for the Treatment of Systemic Lupus Erythematosus
AU - Sammaritano, Lisa R.
AU - Askanase, Anca
AU - Bermas, Bonnie L.
AU - Dall'Era, Maria
AU - Duarte-García, Alí
AU - Hiraki, Linda T.
AU - Son, Mary Beth F.
AU - Werth, Victoria P.
AU - Aranow, Cynthia
AU - Barnado, April
AU - Broder, Anna
AU - Brunner, Hermine I.
AU - Chong, Benjamin F.
AU - Chowdhary, Vaidehi R.
AU - Hersh, Aimee O.
AU - Izmirly, Peter M.
AU - Jules, Marimee
AU - Kalunian, Kenneth
AU - Kamen, Diane
AU - Rubinstein, Tamar B.
AU - Smith, Benjamin J.
AU - Smith, Natalie M.
AU - Thomas, Asha
AU - Timlin, Homa
AU - Wallace, Daniel J.
AU - Azzam, Muayad
AU - Bartels, Christie M.
AU - Cunha, Joanne S.
AU - DeQuattro, Kimberly
AU - Fava, Andrea
AU - Figueroa-Parra, Gabriel
AU - Garg, Shivani
AU - Gomes, Lais Lopes Almeida
AU - Cuéllar-Gutiérrez, Maria C.
AU - Iyer, Priyanka
AU - Johannemann, Andrew S.
AU - Jorge, April
AU - Kasturi, Shanthini
AU - Kawtharany, Hassan
AU - Khawandi, Jana
AU - Legge, Alexandra
AU - Liang, Kimberly P.
AU - Lockwood, Megan M.
AU - Sanchez-Rodriguez, Alain
AU - Turgunbaev, Marat
AU - Williams, Jessica N.
AU - Turner, Amy S.
AU - Mustafa, Reem A.
N1 - Publisher Copyright:
© 2025 American College of Rheumatology.
PY - 2025
Y1 - 2025
N2 - Objective: To provide evidence-based and expert guidance for the treatment and management of non-renal systemic lupus erythematosus (SLE); treatment and management of lupus nephritis are addressed in a separate guideline. Methods: Clinical questions for treatment and management of SLE were developed in the PICO format (population, intervention, comparator, and outcome). Systematic literature reviews were developed for each PICO question, and the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) methodology was used to assess evidence quality and formulate recommendations. The Voting Panel achieved a consensus of ≥70% agreement on the direction (for or against) and strength (strong or conditional) of each recommendation. Results: We present recommendations and ungraded, consensus-based good practice statements for the treatment and management of SLE that are applicable to pediatric and adult patients. Recommendations emphasize uniform treatment with hydroxychloroquine, limiting duration of glucocorticoid use, and early introduction of conventional and/or biologic immunosuppressive therapies to achieve and maintain control of SLE inflammation (remission or a low level of disease activity), reduce SLE-related morbidity and mortality, and minimize medication-related toxicities. Conclusion: This guideline presents direction regarding treatment and management of SLE and provides a foundation for well-informed, shared clinician–patient decision-making. These recommendations should not be used to limit or deny access to therapies, as treatment decisions may vary due to the unique clinical situation and personal preferences of each person with SLE.
AB - Objective: To provide evidence-based and expert guidance for the treatment and management of non-renal systemic lupus erythematosus (SLE); treatment and management of lupus nephritis are addressed in a separate guideline. Methods: Clinical questions for treatment and management of SLE were developed in the PICO format (population, intervention, comparator, and outcome). Systematic literature reviews were developed for each PICO question, and the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) methodology was used to assess evidence quality and formulate recommendations. The Voting Panel achieved a consensus of ≥70% agreement on the direction (for or against) and strength (strong or conditional) of each recommendation. Results: We present recommendations and ungraded, consensus-based good practice statements for the treatment and management of SLE that are applicable to pediatric and adult patients. Recommendations emphasize uniform treatment with hydroxychloroquine, limiting duration of glucocorticoid use, and early introduction of conventional and/or biologic immunosuppressive therapies to achieve and maintain control of SLE inflammation (remission or a low level of disease activity), reduce SLE-related morbidity and mortality, and minimize medication-related toxicities. Conclusion: This guideline presents direction regarding treatment and management of SLE and provides a foundation for well-informed, shared clinician–patient decision-making. These recommendations should not be used to limit or deny access to therapies, as treatment decisions may vary due to the unique clinical situation and personal preferences of each person with SLE.
UR - https://www.scopus.com/pages/publications/105021025888
U2 - 10.1002/art.43452
DO - 10.1002/art.43452
M3 - Article
C2 - 41187097
AN - SCOPUS:105021025888
SN - 2326-5191
JO - Arthritis and Rheumatology
JF - Arthritis and Rheumatology
ER -