# Rituximab Treatment in Lupus Nephritis Resistant to Conventional Therapy: A Single-Centre Experience

**Authors:** Esra F. Senturk, Hande Ogun, Ibrahim Durucan, Berna Yurttas, Serdal Ugurlu

PMC · DOI: 10.31138/mjr.250124.rtl · Mediterranean Journal of Rheumatology · 2025-01-23

## TL;DR

This study shows that Rituximab can effectively reduce kidney inflammation and steroid use in lupus patients who don't respond to standard treatments.

## Contribution

The study provides new evidence on the long-term efficacy and safety of Rituximab in treatment-resistant lupus nephritis.

## Key findings

- Rituximab significantly reduced proteinuria from 3050mg/day to 747mg/day.
- SLEDAI-2K scores decreased significantly from 16.3 to 7.2.
- Steroid doses were reduced from 24.13mg/day to 7.5mg/day.

## Abstract

Treatment-resistant lupus nephritis (LN) is a challenging condition, often causing significant morbidity. While midterm outcomes of anti-CD20 therapies are well-studied, their long-term effects remain unclear.

To assess Rituximab’s long-term efficacy and safety in patients with refractory LN.

The study, conducted retrospectively at a single centre between 2010–2022, included lupus nephritis patients who met the American College of Rheumatology’s criteria for SLE. We evaluated 24-hour proteinuria, creatinine clearance, serum creatinine, and SLEDAI-2K, before and after rituximab treatment. The primary endpoints as a response to treatment were defined as the attainment of a prednisolone dose of 5mg and 24-hour proteinuria of 500mg. Additionally, we investigated any adverse effects of Rituximab.

Patients (34 females, 13 males; mean age 42.3 years; mean disease duration 10.4 years) received a median 3 of rituximab courses. Before treatment, median amount of proteinuria was 3050mg/day. Following the final course of rituximab, the median amount of proteinuria significantly decreased to 747mg/day (p<0.001). SLEDAI-2K score also reduced significantly, from 16.3±6.2 to 7.2±4.8 (p<0.001). The mean steroid dose in the final rituximab course was 7.5±5.8 mg/day (p<0.001), compared to the initial dose of 24.13±18.47mg/day. At primary endpoint, 53.1% of patients achieved a prednisolone dose of 5mg, 36.1% had a 24-hour proteinuria level of 500mg, and 25.5% met both criteria.

Rituximab significantly improved disease activity in lupus nephritis patients, reducing proteinuria, SLEDAI-2K scores, and allowing for steroid dose reduction. Given its efficacy and safety, rituximab may be a promising option for patients resistant to conventional therapy.

## Linked entities

- **Chemicals:** prednisolone (PubChem CID 5755)
- **Diseases:** lupus nephritis (MONDO:0005556)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}
- **Diseases:** proteinuria (MESH:D011507), LN (MESH:D008181), SLE (MESH:D008180)
- **Chemicals:** Rituximab (MESH:D000069283), creatinine (MESH:D003404), steroid (MESH:D013256), prednisolone (MESH:D011239)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12312482/full.md

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Source: https://tomesphere.com/paper/PMC12312482