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Title: | Comparison of disease activity between tacrolimus and mycophenolate mofetil in lupus nephritis: a randomized controlled trial |
Authors: | Kamanamool N. Ingsathit A. Rattanasiri S. Ngamjanyaporn P. Kasitanont N. Chawanasuntorapoj R. Pichaiwong W. Anutrakulchai S. Sangthawan P. Ophascharoensuk V. Avihingsanon Y. Sumethkul V. |
Keywords: | antinuclear antibody azathioprine creatinine double stranded DNA antibody mycophenolate mofetil prednisolone prednisone tacrolimus immunosuppressive agent mycophenolic acid tacrolimus adult Article clinical outcome controlled study creatinine blood level disease activity disease activity score disease severity drug blood level drug dose reduction female hematuria histopathology human human tissue large intestine perforation lupus erythematosus nephritis maintenance therapy major clinical study male multicenter study nocardiosis open study plasmablastic lymphoma Pneumocystis pneumonia priority journal prospective study proteinuria randomized controlled trial remission septic shock SLEDAI treatment outcome biopsy clinical trial comparative study immunology Kaplan Meier method lupus erythematosus nephritis middle aged severity of illness index Thailand time factor young adult Adult Biopsy Female Humans Immunosuppressive Agents Kaplan-Meier Estimate Lupus Nephritis Male Middle Aged Mycophenolic Acid Prospective Studies Remission Induction Severity of Illness Index Tacrolimus Thailand Time Factors Treatment Outcome Young Adult |
Issue Date: | 2018 |
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. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/13654 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044406119&doi=10.1177%2f0961203317739131&partnerID=40&md5=f59b4a94a60bf5ac82e7b58c94ff0c22 |
ISSN: | 9612033 |
Appears in Collections: | Scopus 1983-2021 |
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