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Abstract Number: 2697

A Prospective Randomized Controlled 96-week Study to Evaluate the Efficacy and Safety of Tacrolimus and Glucocorticoid as Continuous Induction-Maintenance Treatment for Class III/IV±V Lupus Nephritis

Sandra Navarra1, Desmond Yat-Hin Yap2, Zhaohui Ni3, Yingyos Avihingsanon4, Soo Kun Lim5, Na Jiang3, Wei Chen6, Chao Li7, Helen Zhi8, Chenzhu Zhang9, Catherine Chan2, Susan Yung2, Tsutomu Takeuchi10 and Tak Mao Daniel Chan2, 1University of Santo Tomas, Manila, Philippines, 2Department of Medicine, The University of Hong Kong, Hong Kong SAR, Hong Kong, 3Renji Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, China (People's Republic), 4King Chulalongkorn Memorial Hospital, Chulalongkorn University, Bangkok, Thailand, 5Department of Medicine, University Malaya Medical Centre, Kuala Lumpur, Malaysia, 6Department of Nephrology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China (People's Republic), 7Department of Nephrology, Peking Union Medical College Hospital, Beijing, China (People's Republic), 8School of Public Health, The University of Hong Kong, Hong Kong SAR, Hong Kong, 9Department of Medicine, University of Hong Kong-Shenzhen Hospital, Shenzhen, China (People's Republic), 10Saitama Medical University and Keio University, Tokyo, Japan

Meeting: ACR Convergence 2025

Keywords: clinical trial, Lupus nephritis

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Session Information

Date: Wednesday, October 29, 2025

Title: Abstracts: Systemic Lupus Erythematosus – Treatment II (2693–2698)

Session Type: Abstract Session

Session Time: 12:30PM-12:45PM

Background/Purpose: Tacrolimus (TAC) and glucocorticoid as continuous induction-maintenance therapy for lupus nephritis (LN) has never been investigated. We conducted a prospective randomized open-label multicenter study to evaluate its efficacy and safety against standard-of-care mycophenolate mofetil (MMF) and glucocorticoid dual immunosuppression in Asian patients with active severe LN.

Methods: Patients with biopsy-proven Class III/IV±V LN were randomized to receive pulse methylprednisolone (500mg/500mg/150mg) for 3 days followed by oral prednisolone (0.7 mg/kg/day, then taper) in combination with either TAC (initial dose 2 mg bid; target trough level 6-8 ng/mL) or MMF (1 g bid), then followed for 96 weeks. Primary endpoint was sustained renal response (SRR) [defined as proteinuria reduced by >50% compared with baseline and 24-hr urine protein < 1 g and serum creatinine not higher than 15% above baseline and no disease flare or rescue therapies] at Week 96. Key secondary endpoints included rates of complete renal response (CR), adverse events, and time-to-renal related adverse events/death.

Results: A total of 130 patients were randomized (65 in each group). TAC and MMF treatment groups showed similar rates of SRR (58.5% vs. 69.2%, OR 0.62; 95% CI 0.29-1.29; p=0.2) and CR (55.4% vs. 63.1%, OR 0.72; p=0.36) at Week 96. SRR rates for TAC and MMF groups were 53.8% vs 52.3% at Week 24, and 63.1% vs. 66.2% at Week 48 respectively (Figure 1). Time-to-renal related adverse events/death were similar in both groups (HR 0.70; 95% CI 0.37-1.35; p=0.29). Overall adverse event rates were 69.2% and 70.8% in TAC and MMF groups respectively (p=1.00), while serious adverse events were more frequent in the MMF group (12.3% vs. 30.8%, p=0.02). Acute kidney injury (16.9% vs. 3.1%) and tremor (16.9% vs. 0%) were more frequent in TAC-treated patients, while leucopoenia (1.5% vs. 12.3%) was more frequent in the MMF group. Three patients in the MMF group died.

Conclusion: Immunosuppressive regimen with TAC combined with glucocorticoid showed comparable efficacy as MMF with glucocorticoid, as continuous induction-maintenance treatment for active LN over 96 weeks, with similar overall adverse event rate but different safety profile between the two treatments.

Supporting image 1Figure 1. Sustained renal response (SRR) rate in patients with active lupus nephritis treated with tacrolimus (TAC) or mycophenolate mofetil (MMF) in combination with glucocorticoid.


Disclosures: S. Navarra: Astellas, 2, 6, AstraZeneca, 2, 6, Aurinia, 2, 6, Biogen, 2, 12, Independent Data Monitoring Committee, Viatris (Idorsia), 2, 6; D. Yap: None; Z. Ni: None; Y. Avihingsanon: Astellas, 6, Novartis, 5; S. Lim: None; N. Jiang: None; W. Chen: None; C. Li: None; H. Zhi: None; C. Zhang: None; C. Chan: None; S. Yung: None; T. Takeuchi: AbbVie, 2, 6, Astellas Pharma, 6, AstraZeneca, 6, Chugai Pharmaceutical, 6, Eisai, 6, Eli Lilly, 2, 6, Gilead Sciences, 2, 6, Janssen, 6, Mitsubishi Tanabe Pharma, 2, 6, Pfizer, 6, Taisho Pharmaceutical, 2, 6; T. Chan: Astellas Pharm Inc, 5, GlaxoSmithKlein(GSK), 2, Novartis, 2.

To cite this abstract in AMA style:

Navarra S, Yap D, Ni Z, Avihingsanon Y, Lim S, Jiang N, Chen W, Li C, Zhi H, Zhang C, Chan C, Yung S, Takeuchi T, Chan T. A Prospective Randomized Controlled 96-week Study to Evaluate the Efficacy and Safety of Tacrolimus and Glucocorticoid as Continuous Induction-Maintenance Treatment for Class III/IV±V Lupus Nephritis [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/a-prospective-randomized-controlled-96-week-study-to-evaluate-the-efficacy-and-safety-of-tacrolimus-and-glucocorticoid-as-continuous-induction-maintenance-treatment-for-class-iii-iv%c2%b1v-lupus-nephr/. Accessed .
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