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Comparison of disease activity between tacrolimus and mycophenolate mofetil in lupus nephritis: a randomized controlled trial

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dc.contributor.author Kamanamool N.
dc.contributor.author Ingsathit A.
dc.contributor.author Rattanasiri S.
dc.contributor.author Ngamjanyaporn P.
dc.contributor.author Kasitanont N.
dc.contributor.author Chawanasuntorapoj R.
dc.contributor.author Pichaiwong W.
dc.contributor.author Anutrakulchai S.
dc.contributor.author Sangthawan P.
dc.contributor.author Ophascharoensuk V.
dc.contributor.author Avihingsanon Y.
dc.contributor.author Sumethkul V.
dc.date.accessioned 2021-04-05T03:25:26Z
dc.date.available 2021-04-05T03:25:26Z
dc.date.issued 2018
dc.identifier.issn 9612033
dc.identifier.other 2-s2.0-85044406119
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/13654
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044406119&doi=10.1177%2f0961203317739131&partnerID=40&md5=f59b4a94a60bf5ac82e7b58c94ff0c22
dc.description.abstract We conducted a prospective multicenter, opened-label, parallel, randomized, controlled trial to compare tacrolimus (TAC) and mycophenolate mofetil (MMF) for induction and maintenance therapy in lupus nephritis (LN). Adult patients with biopsy-proven LN International Society of Nephrology/Renal Pathology Society classes III–V and active nephritis were to receive prednisolone (0.7–1.0 mg/kg/day for four weeks of run-in period and tapered) and randomly assigned to receive TAC (0.1 mg/kg/day) or MMF (1.5–2 g/day) as induction therapy for six months. All patients who had remission received azathioprine (AZA) 1–2 mg/kg/day as standard treatment in the maintenance phase. The primary outcome was Systemic Lupus Erythematosus Disease Activity Index-2000 (SLEDAI-2K) at six and 12 months, and the secondary outcomes included renal SLEDAI, non-renal SLEDAI, modified SLEDAI-2K, immunity SLEDAI, and disease activity remission. Eighty-four patients were randomized. One patient who was randomized to the TAC group withdrew from the study immediately after randomization. Therefore, 42 patients received MMF and 41 patients received TAC. Disease activity remission rate and time to disease activity remission were similar in both groups. Twelve patients (28.57%) in the MMF group and 10 patients (24.39%) in the TAC group achieved disease activity remission. For disease activity scores, both regimens significantly improved SLEDAI-2K during induction and maintenance therapy. Overall, SLEDAI-2K score in the MMF group decreased more compared with the TAC group. In the MMF group, mean SLEDAI-2K decreased from 11.6 ± 4.8 to 6.3 ± 3.9 after induction therapy and to 5.4 ± 4.4 after maintenance therapy. In the TAC group, mean SLEDAI-2K decreased from 9.0 ± 3.7 to 6.3 ± 5.1 after induction therapy and to 7.1 ± 5.4 after maintenance therapy. Renal SLEDAI and modified SLEDAI-2K showed a similar pattern with SLEDAI-2K. In non-renal SLEDAI and immunity SLEDAI, both regimens also resulted in decreased disease activity scores during the first two months. After that the scores were slightly increased. In the MMF group, the scores were still lower than baseline but in the TAC group were not. In conclusion, disease activity remission rate was similar in the MMF and TAC groups. For disease activity score as measured by SLEDAI-2K, TAC was comparable with MMF during induction but MMF was more effective on disease activity of active LN classes III and IV at 12 months, especially in the renal system. © 2017, © The Author(s) 2017.
dc.subject antinuclear antibody
dc.subject azathioprine
dc.subject creatinine
dc.subject double stranded DNA antibody
dc.subject mycophenolate mofetil
dc.subject prednisolone
dc.subject prednisone
dc.subject tacrolimus
dc.subject immunosuppressive agent
dc.subject mycophenolic acid
dc.subject tacrolimus
dc.subject adult
dc.subject Article
dc.subject clinical outcome
dc.subject controlled study
dc.subject creatinine blood level
dc.subject disease activity
dc.subject disease activity score
dc.subject disease severity
dc.subject drug blood level
dc.subject drug dose reduction
dc.subject female
dc.subject hematuria
dc.subject histopathology
dc.subject human
dc.subject human tissue
dc.subject large intestine perforation
dc.subject lupus erythematosus nephritis
dc.subject maintenance therapy
dc.subject major clinical study
dc.subject male
dc.subject multicenter study
dc.subject nocardiosis
dc.subject open study
dc.subject plasmablastic lymphoma
dc.subject Pneumocystis pneumonia
dc.subject priority journal
dc.subject prospective study
dc.subject proteinuria
dc.subject randomized controlled trial
dc.subject remission
dc.subject septic shock
dc.subject SLEDAI
dc.subject treatment outcome
dc.subject biopsy
dc.subject clinical trial
dc.subject comparative study
dc.subject immunology
dc.subject Kaplan Meier method
dc.subject lupus erythematosus nephritis
dc.subject middle aged
dc.subject severity of illness index
dc.subject Thailand
dc.subject time factor
dc.subject young adult
dc.subject Adult
dc.subject Biopsy
dc.subject Female
dc.subject Humans
dc.subject Immunosuppressive Agents
dc.subject Kaplan-Meier Estimate
dc.subject Lupus Nephritis
dc.subject Male
dc.subject Middle Aged
dc.subject Mycophenolic Acid
dc.subject Prospective Studies
dc.subject Remission Induction
dc.subject Severity of Illness Index
dc.subject Tacrolimus
dc.subject Thailand
dc.subject Time Factors
dc.subject Treatment Outcome
dc.subject Young Adult
dc.title Comparison of disease activity between tacrolimus and mycophenolate mofetil in lupus nephritis: a randomized controlled trial
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Lupus. Vol 27, No.4 (2018), p.647-656
dc.identifier.doi 10.1177/0961203317739131


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