ArticleKidney international reports2025
Efficacy of Rituximab as Adjunctive Therapy to Immunosuppressive Agents in Adult Primary Focal Segmental Glomerulosclerosis.
Article in Kidney international reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Is There a Role for Rituximab in FSGS Therapy in Adults?Kidney international reports · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
17 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Primary focal segmental glomerulosclerosis (FSGS) is a rare, likely immune-related disease. Rituximab (RTX) may help manage it, but existing adult data are limited and mainly based on case reports or case series. We aimed to evaluate RTX treatment outcomes in a large, multicenter adult cohort. Methods: This was a retrospective study of 160 patients with primary FSGS treated with RTX as adjunctive therapy to standard immunosuppressive agents between March 2015 and June 2023, that evaluated treatment responses at 3, 6, and 12 months, followed by an extended 24-month follow-up to assess long-term outcomes. Treatment outcomes included complete response (CR), partial response (PR), or no response. Treatment-related adverse effects and relapse-free survival (RFS) were evaluated at each visit. Patients undergoing RTX retreatment and those monitored for an extended 24-month period were analyzed independently. Results: Response rates at 3, 6, and 12 months were 57%, 71%, and 74%, respectively. Twelve-month RTX response was positively associated with lower baseline 24-hour proteinuria (odds ratio [OR] = 0.49, Conclusion: RTX shows promise in treating primary FSGS, particularly in steroid-dependent patients, those with less severe nephrotic syndrome, and previous responders. RTX offers durable responses for most patients, but long-term management remains challenging in those who relapse and need retreatment.
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