TY - JOUR
T1 - Association of Modified Systemic Lupus Erythematosus Responder Index Attainment With Long-Term Clinical Outcomes
T2 - A Five-Year Prospective Study
AU - Connelly, Kathryn
AU - Kandane-Rathnayake, Rangi
AU - Hoi, Alberta
AU - Louthrenoo, Worawit
AU - Hamijoyo, Laniyati
AU - Luo, Shue Fen
AU - Wu, Yeong Jian Jan
AU - Cho, Jiacai
AU - Lateef, Aisha
AU - Lau, C. S.
AU - Chen, Yi Hsing
AU - Navarra, Sandra
AU - Zamora, Leonid
AU - Li, Zhanguo
AU - An, Yuan
AU - Sockalingam, Sargunan
AU - Hao, Yanjie
AU - Zhang, Zhuoli
AU - Chan, Madelynn
AU - Katsumata, Yasuhiro
AU - Harigai, Masayoshi
AU - Oon, Shereen
AU - Bae, Sang Cheol
AU - O'Neill, Sean
AU - Gibson, Kathryn A.
AU - Basnayake, B. M.D.B.
AU - Kikuchi, Jun
AU - Takeuchi, Tsutomu
AU - Ng, Kristine Pek Ling
AU - Tugnet, Nicola
AU - Kumar, Sunil
AU - Goldblatt, Fiona
AU - Law, Annie
AU - Tee, Michael
AU - Tee, Cherica
AU - Tanaka, Yoshiya
AU - Ohkubo, Naoaki
AU - Tan, Jin Yu
AU - Karyekar, Chetan S.
AU - Nikpour, Mandana
AU - Golder, Vera
AU - Morand, Eric F.
N1 - Publisher Copyright:
© 2022 The Authors. Arthritis & Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology.
PY - 2023/3
Y1 - 2023/3
N2 - Objective: In trials of systemic lupus erythematosus (SLE), the SLE Responder Index (SRI) is the most commonly used primary efficacy end point but has limited validation against long-term outcomes. We aimed to investigate associations of attainment of a modified version of the SRI (mSRI) with key clinical outcomes in SLE patients with up to 5 years of follow-up. Methods: We used data from a large multicenter, longitudinal SLE cohort in which patients received standard of care. The first visit with active disease (defined as SLE Disease Activity Index 2000 [SLEDAI-2K] score ≥6) was designated as baseline, and mSRI attainment (defined as a reduction in SLEDAI-2K ≥4 points with no worsening in physician global assessment ≥0.3 points) was determined at annual intervals from baseline up to 5 years. Associations between mSRI attainment and outcomes including disease activity, glucocorticoid dose, flare, damage accrual, Lupus Low Disease Activity State (LLDAS), and remission were studied. Results: We included 2,060 patients, with a median baseline SLEDAI-2K score of 8. An mSRI response was attained by 56% of patients at 1 year, with similar responder rates seen at subsequent annual time points. Compared to nonresponders, mSRI responders had significantly lower disease activity and prednisolone dose and higher proportions of LLDAS and remission attainment at each year, and less damage accrual at years 2 and 3. Furthermore, mSRI responder status at 1 year predicted clinical benefit at subsequent years across most outcomes, including damage accrual (odds ratio [OR] range 0.58–0.69, P < 0.05 for damage accrual ORs at all time points). Conclusion: In SLE patients with active disease receiving standard of care, mSRI attainment predicts favorable outcomes over long-term follow-up, supporting the clinical meaningfulness of SRI attainment as an SLE trial end point.
AB - Objective: In trials of systemic lupus erythematosus (SLE), the SLE Responder Index (SRI) is the most commonly used primary efficacy end point but has limited validation against long-term outcomes. We aimed to investigate associations of attainment of a modified version of the SRI (mSRI) with key clinical outcomes in SLE patients with up to 5 years of follow-up. Methods: We used data from a large multicenter, longitudinal SLE cohort in which patients received standard of care. The first visit with active disease (defined as SLE Disease Activity Index 2000 [SLEDAI-2K] score ≥6) was designated as baseline, and mSRI attainment (defined as a reduction in SLEDAI-2K ≥4 points with no worsening in physician global assessment ≥0.3 points) was determined at annual intervals from baseline up to 5 years. Associations between mSRI attainment and outcomes including disease activity, glucocorticoid dose, flare, damage accrual, Lupus Low Disease Activity State (LLDAS), and remission were studied. Results: We included 2,060 patients, with a median baseline SLEDAI-2K score of 8. An mSRI response was attained by 56% of patients at 1 year, with similar responder rates seen at subsequent annual time points. Compared to nonresponders, mSRI responders had significantly lower disease activity and prednisolone dose and higher proportions of LLDAS and remission attainment at each year, and less damage accrual at years 2 and 3. Furthermore, mSRI responder status at 1 year predicted clinical benefit at subsequent years across most outcomes, including damage accrual (odds ratio [OR] range 0.58–0.69, P < 0.05 for damage accrual ORs at all time points). Conclusion: In SLE patients with active disease receiving standard of care, mSRI attainment predicts favorable outcomes over long-term follow-up, supporting the clinical meaningfulness of SRI attainment as an SLE trial end point.
UR - http://www.scopus.com/inward/record.url?scp=85142475376&partnerID=8YFLogxK
U2 - 10.1002/art.42350
DO - 10.1002/art.42350
M3 - Article
C2 - 36122172
AN - SCOPUS:85142475376
SN - 2326-5191
VL - 75
SP - 401
EP - 410
JO - Arthritis & Rheumatology
JF - Arthritis & Rheumatology
IS - 3
ER -