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Cited 8 time in webofscience Cited 9 time in scopus
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Efficacy and safety of mycophenolate mofetil and tacrolimus combination therapy in patients with lupus nephritis: a nationwide multicentre study

Authors
Park, D-JKang, J-HLee, K-EBae, S-CChung, W-TChoe, J-YJung, S-YKim, Y-SLee, H-SLee, J.Lee, Y-APark, S-HPark, Y-JSuh, C-HYoo, D-HLee, S-S
Issue Date
Jan-2019
Publisher
CLINICAL & EXPER RHEUMATOLOGY
Keywords
combination therapy; complete remission; lupus nephritis; mycophenolate mofetil; tacrolimus
Citation
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, v.37, no.1, pp.89 - 96
Indexed
SCIE
SCOPUS
Journal Title
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
Volume
37
Number
1
Start Page
89
End Page
96
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/15162
ISSN
0392-856X
Abstract
Objective Recent studies have shown that a combination treatment of mycophenolate mofetil (MMF) and tacrolimus (TAC) may be an option for lupus nephritis (LN) patients that do not adequately respond to initial treatment. We evaluated the efficacy and safety of the combination treatment of MMF and TAC in LN patients with suboptimal response to prior MMF or TAC treatments. Methods In this multicentre study, we retrospectively enrolled 62 patients with class III, IV, or V LN who inadequately responded to MMF or TAC treatment. Those patients were then treated with a combination of MMF and TAC for 6 months. The primary outcome was complete remission (CR) at 6 months, and secondary outcomes included overall response and adverse events. Results After 6 months of treatment with the drug combination, CR was achieved in 14 of 62 patients (22.6%), and 35 (56.5%) patients responded. A significant reduction in proteinuria and lupus disease activity score was observable after 3 months. After 1 year, the CR rate increased to.36.4% (20 of 55 patients), and the overall response rate (n=38, 69.1%) also increased from 6 months. Twenty-one patients reported 29 adverse events, including severe infection requiring hospitalisation (n=3, 10.3%), infection not requiring hospitalisation (n=2, 6.9% ), and herpes zoster (n=4, 13.8%). Conclusion Our findings suggest that a combined MMF and TAC treatment, with a favourable adverse-event profile, may be a beneficial option for LN patients with inadequate response to either MMF or TAC treatments.
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