Abstract: TH-OR068
Treatment Patterns, Response, and Relapse in Minimal Change Disease: A US Registry Study
Session Information
- Glomerular Diseases: Epidemiology and Real-World Outcomes
October 22, 2026 | Location: Room 501, Convention Center
Abstract Time: 05:10 PM - 05:20 PM
Category: Glomerular Diseases
- 1402 Glomerular Diseases: Clinical, Outcomes, and Therapeutics
Authors
- Lewing, Benjamin, Otsuka Pharmaceutical Development and Commercialization Inc, Princeton, New Jersey, United States
- Khan, Anam M., RTI Health Solutions, Durham, North Carolina, United States
- Helmuth, Margaret, University of Michigan, Ann Arbor, Michigan, United States
- Layton, J. Bradley, RTI Health Solutions, Durham, North Carolina, United States
- Dellepiane, Sergio, Otsuka Pharmaceutical Development and Commercialization Inc, Princeton, New Jersey, United States
- Demas, Caroline, University of Michigan, Ann Arbor, Michigan, United States
- Gidey, Saba, Otsuka Pharmaceutical Development and Commercialization Inc, Princeton, New Jersey, United States
- Mariani, Laura H., University of Michigan, Ann Arbor, Michigan, United States
Background
Minimal change disease (MCD) is a histologic lesion associated with immune-mediated nephrotic syndrome (NS), characterized by frequent relapse. This study describes demographics, clinical characteristics, treatment patterns, and outcomes among participants with MCD.
Methods
Participants aged ≥18 years from the United States with a biopsy showing evidence of MCD were identified in the CureGN Glomerular Disease Registry (2014-2024). The biopsy date was the index date. Participants with evidence of NS before biopsy were included; those with long-term corticosteroid use at the time of biopsy were excluded so that initial treatment response could be observed. Follow-up began the day after biopsy and ended at registry disenrollment, end of available data, or death. Among participants who initiated corticosteroids within 1 year of biopsy and had recorded urine protein-to-creatinine ratio (UPCR) measurements at baseline and ≥1 follow-up measurement within 8 months of initiation, treatment response was classified as complete response (CR; UPCR <0.3 g/g), partial response (PR; UPCR 0.3–3.5 g/g and <50% of baseline), or none. Responders (CR/PR) were followed to evaluate relapse using subsequent UPCR measurements. Times to response and relapse were summarized descriptively.
Results
A total of 77 eligible participants with MCD were identified. At biopsy, median age was 45.0 years, 66% were female, and median (interquartile range [IQR]) estimated glomerular filtration rate was 81.8 (65.7-105.7) mL/min/1.73m2. Fifty-two participants initiated corticosteroids within 1 year of biopsy (mean time to initiation, 28 days [standard deviation, 60]); within 12 months of corticosteroid initiation, 56% of participants had added another immunosuppressant. Among corticosteroid initiators, 35 individuals had available UPCR data for response assessment; 88.6% responded (CR, 71.4%; PR, 17.1%), with median (IQR) time to response of 53 days (28-135). Among responders, 43% relapsed within 1 year and 63% within 2 years; median (IQR) time to relapse was 166 days (40-441).
Conclusion
Most participants with MCD initiated corticosteroids soon after biopsy and had high response rates; however, relapse was common and many received additional immunosuppression. Findings highlight the challenges of identifying effective therapy for patients with MCD and emphasize the need for therapies that induce durable remission and reduce relapse.
Funding
- Commercial Support – Otsuka Pharmaceutical Development and Commercialization, Inc.