Abstract: SA-PO0839
Long-Term Outcomes Following Combination Therapy of Rituximab, Low-Dosage Cyclophosphamide, and Prednisone for Membranous Nephropathy
Session Information
- Glomerular Management: Real-World Lessons and Emerging Therapies
November 08, 2025 | Location: Exhibit Hall, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Glomerular Diseases
- 1402 Glomerular Diseases: Clinical, Outcomes, and Therapeutics
Authors
- Aaron, Sydney, Massachusetts General Hospital, Boston, Massachusetts, United States
- Seethapathy, Harish Shanthanu, Massachusetts General Hospital, Boston, Massachusetts, United States
- Jeyabalan, Anushya, Massachusetts General Hospital, Boston, Massachusetts, United States
- Al Jurdi, Ayman, Massachusetts General Hospital, Boston, Massachusetts, United States
- Sauvage, Gabriel, Massachusetts General Hospital, Boston, Massachusetts, United States
- Chung, James L., Massachusetts General Hospital, Boston, Massachusetts, United States
- Zonozi, Reza, Nephrology Associates of Northern Virginia, Fairfax, Virginia, United States
- Laliberte, Karen A., Massachusetts General Hospital, Boston, Massachusetts, United States
- Niles, John, Massachusetts General Hospital, Boston, Massachusetts, United States
- Efe, Orhan, Massachusetts General Hospital, Boston, Massachusetts, United States
Group or Team Name
- Vasculitis and Glomerulonephritis Center.
Background
Relapse remains a significant challenge in primary membranous nephropathy (MN). Combination of rituximab (RTX), low-dose oral cyclophosphamide (CYC), and prednisone has demonstrated promising efficacy, but longer-term outcomes and relapse risk need further investigation.
Methods
This is a single-center retrospective study of patients with MN who completed combination therapy with RTX x 2 years, low-dose CYC x 8 weeks, and short prednisone taper x 4 months at the Vasculitis and Glomerulonephritis Center at Mass General Hospital. Patients with >1 year follow-up after completing RTX were included. Primary outcome was relapse after complete or partial remission, defined as achieving UPCR <0.3 g/g with stable eGFR or UPCR <3.0 g/g with a ≥50% fall from baseline, respectively.
Results
66 patients were included. Patient characteristics are in Table 1. 32% (21/66) of patients had relapsing disease before combination therapy. 100% of patients achieved at least partial remission after combination therapy. During a median 4.3 (IQR 3.2-6.9) years of follow-up from last RTX, 18% (12/66) had a relapse. 92% (11/12) were anti-PLA2R positive. By Kaplan-Meier analysis, risk of relapse since final RTX was 3% at 2 years, 11% at 4 years, and 24% at 5 years (Fig.1). At relapse, median peak proteinuria was 3.7 (2.3-5.2) g/g. Following relapse, all 12 patients were retreated with RTX at median 5 infusions, including 5 who also received CYC and prednisone. All relapse patients achieved partial or complete remission. Of the 12 patients who relapsed, 33% (n=4) had at least 1 more subsequent relapse during B-cell repopulation, 1 of whom received combination therapy after prior relapse.
Conclusion
Risk of relapse is reduced by combination therapy for MN. Retreatment with RTX mono- or combination therapies is effective for relapsing disease.