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