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Rituximab Shows Long-Term Remission in Pediatric Steroid-Dependent Nephrotic Syndrome

Rituximab Shows Long-Term Remission in Pediatric Steroid-Dependent Nephrotic Syndrome
Photo by Ayanda Kunene / Unsplash
Key Takeaway
Consider rituximab as a potential option for reducing relapses in pediatric steroid-dependent nephrotic syndrome, but evidence is limited by retrospective design.

This retrospective cohort study evaluated long-term outcomes of rituximab in 42 pediatric patients with steroid-dependent or frequently relapsing nephrotic syndrome due to minimal change disease (MCD) or focal segmental glomerulosclerosis (FSGS). Patients received a median of 4 rituximab infusions (IQR 3-5) and were followed for up to 6 years.

All 42 patients (100%) achieved clinical remission, and 38 (90.5%) attained complete remission. Within the first year after the first rituximab dose, relapse rates decreased to 35.7%, and the median number of relapses dropped from 2 to 0. No significant difference in relapse rates was observed between patients receiving 3-4 doses versus 1-2 doses.

At 96 months, relapse-free survival was 33.3% (2/6) in the FSGS group and 41.7% (15/36) in the MCD group, though the p-value was not reported, making comparisons uncertain. Safety data were not reported.

Key limitations include the retrospective design, small sample size, single-center setting, and unbalanced group sizes (MCD vs. FSGS). Due to the observational nature, causality cannot be established, and findings should be interpreted with caution. The study suggests rituximab may be effective in reducing relapses in this population, but higher-quality evidence is needed.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
BackgroundRituximab has been shown efficacy in reducing relapses among patients with steroid-dependent or frequently relapsing nephrotic syndrome (SDNS/FRNS), primarily due to minimal change disease (MCD) or focal segmental glomerulosclerosis (FSGS). However, whether its efficacy differs between these two histological subtypes remains unclear.MethodsA retrospective cohort study included 42 pediatric SDNS/FRNS patients with biopsy-proven MCD or FSGS. Clinical outcomes, including remission rates and relapse frequency were assessed.ResultsThe median age at diagnosis of the 42 patients was 5.1 years (IQR: 2.9–7.4), and 28 (67%) patients were male during the 6-year follow-up. Each patient received a median of 4 (IQR: 3–5) infusions. All patients achieved clinical remission, with 90.5% attaining complete remission. Relapse times decreased to 35.7% within 1 year after the first rituximab treatment, from a median of 2 relapses to 0. No significant difference in relapse rates was observed between patients receiving 3–4 doses versus 1–2 doses during the initial course. Histologically, 36 patients (85.7%) had MCD and 6 (14.3%) had FSGS. In the FSGS group, the 96-month relapse-free survival was higher compared to MCD controls (2/6 [33.3%] vs. 15/36 [41.7%]; p
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