TY - JOUR
T1 - Patterns of Medication Use in Systemic Lupus Erythematosus
T2 - A Multicenter Cohort Study
AU - Kandane-Rathnayake, Rangi
AU - Louthrenoo, Worawit
AU - Luo, Shue Fen
AU - Wu, Yeong Jian J.
AU - Chen, Yi Hsing
AU - Golder, Vera
AU - Lateef, Aisha
AU - Cho, Jiacai
AU - Navarra, Sandra V.
AU - Zamora, Leonid
AU - Hamijoyo, Laniyati
AU - Sockalingam, Sargunan
AU - An, Yuan
AU - Li, Zhanguo
AU - Montes, Ricardo
AU - Oon, Shereen
AU - Katsumata, Yasuhiro
AU - Harigai, Masayoshi
AU - Hao, Yanjie
AU - Zhang, Zhuoli
AU - Chan, Madelynn
AU - Kikuchi, Jun
AU - Takeuchi, Tsutomu
AU - Goldblatt, Fiona
AU - O'Neill, Sean
AU - Bae, Sang Cheol
AU - Lau, Chak S.
AU - Hoi, Alberta
AU - Karyekar, Chetan S.
AU - Nikpour, Mandana
AU - Morand, Eric F.
AU - for the Asia Pacific Lupus Collaboration
N1 - Funding Information:
Supported by Janssen Research and Development. The Asia‐Pacific Lupus Collaboration received unrestricted project grants from AstraZeneca, Bristol Myers Squibb, Merck Serono, GlaxoSmithKline, Eli Lilly and Company, and UCB in support of data collection contributing to this work.
Publisher Copyright:
© 2021 American College of Rheumatology.
PY - 2022/12
Y1 - 2022/12
N2 - Objective: Evidence for the utility of medications in settings lacking randomized trial data can come from studies of treatment persistence. The present study was undertaken to examine patterns of medication use in systemic lupus erythematosus (SLE) using data from a large multicenter longitudinal cohort. Methods: Prospectively collected data from the Asia Pacific Lupus Collaboration cohort including disease activity (SLE Disease Activity Index 2000 [SLEDAI-2K]) and medication details, captured at every visit from 2013–2018, were used. Medications were categorized as glucocorticoids (GCs), antimalarials (AM), and immunosuppressants (IS). Cox regression analyses were performed to determine the time-to-discontinuation of medications, stratified by SLE disease activity. Results: Data from 19,804 visits of 2,860 patients were analyzed. Eight medication categories were observed: no treatment; GC, AM, or IS only; GC plus AM; GC plus IS; AM plus IS; and GC plus AM plus IS (triple therapy). Triple therapy was the most frequent pattern (31.4% of visits); single agents were used in 21% of visits, and biologics in only 3%. Time-to-discontinuation analysis indicated that medication persistence varied widely, with the highest treatment persistence for AM and lowest for IS. Patients with a time-adjusted mean SLEDAI-2K score of ≥10 had lower discontinuation of GCs and higher discontinuation of IS. Conclusion: Most patients received combination treatment. GC persistence was high, while IS persistence was low. Patients with high disease activity received more medication combinations but had reduced IS persistence, consistent with limited utility. These data confirm unmet need for improved SLE treatments.
AB - Objective: Evidence for the utility of medications in settings lacking randomized trial data can come from studies of treatment persistence. The present study was undertaken to examine patterns of medication use in systemic lupus erythematosus (SLE) using data from a large multicenter longitudinal cohort. Methods: Prospectively collected data from the Asia Pacific Lupus Collaboration cohort including disease activity (SLE Disease Activity Index 2000 [SLEDAI-2K]) and medication details, captured at every visit from 2013–2018, were used. Medications were categorized as glucocorticoids (GCs), antimalarials (AM), and immunosuppressants (IS). Cox regression analyses were performed to determine the time-to-discontinuation of medications, stratified by SLE disease activity. Results: Data from 19,804 visits of 2,860 patients were analyzed. Eight medication categories were observed: no treatment; GC, AM, or IS only; GC plus AM; GC plus IS; AM plus IS; and GC plus AM plus IS (triple therapy). Triple therapy was the most frequent pattern (31.4% of visits); single agents were used in 21% of visits, and biologics in only 3%. Time-to-discontinuation analysis indicated that medication persistence varied widely, with the highest treatment persistence for AM and lowest for IS. Patients with a time-adjusted mean SLEDAI-2K score of ≥10 had lower discontinuation of GCs and higher discontinuation of IS. Conclusion: Most patients received combination treatment. GC persistence was high, while IS persistence was low. Patients with high disease activity received more medication combinations but had reduced IS persistence, consistent with limited utility. These data confirm unmet need for improved SLE treatments.
UR - http://www.scopus.com/inward/record.url?scp=85136528229&partnerID=8YFLogxK
U2 - 10.1002/acr.24740
DO - 10.1002/acr.24740
M3 - Article
C2 - 34197023
AN - SCOPUS:85136528229
SN - 2151-464X
VL - 74
SP - 2033
EP - 2041
JO - Arthritis Care & Research
JF - Arthritis Care & Research
IS - 12
ER -