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RITUXIMAB IN REFRACTORY SLE: 10 YEARS AFTER

2025· article· en· W4410512949 on OpenAlexvenueno aff
Chrysanthi Staveri, Chrysa Lykoura, Constantinos Melissaropoulos, Stamatis‐Nick C. Liossis

Bibliographic record

VenueThe Journal of Rheumatology · 2025
Typearticle
Languageen
FieldMedicine
TopicSystemic Sclerosis and Related Diseases
Canadian institutionsnot available
Fundersnot available
KeywordsMedicineRituximabRefractory (planetary science)DermatologyInternal medicineLymphoma

Abstract

fetched live from OpenAlex

PV275 / #231 Poster Topic: AS24 - SLE-Treatment Background/Purpose The aim of this cross-sectional study of patients with refractory SLE treated with RTX was to explore for any potential long-term effect(s) of this B cell depletion approach. Methods We included patients with SLE having had i) received at least 1 cycle of RTX and ii) at least 10yr of follow-up after their first RTX infusion. Response was assessed at 1 year and at their latest evaluation that was ³ 10yr after RTX treatment initiation. In cases where the cSLEDAI-2k was employed, a response was defined as a cSLEDAI-2k of less than 4 in cases were the cSLEDAI-2k was ³ 4. In cases where the cSLEDAI-2k was 2-4 at baseline, a response was defined as a cSLEDAI-2k of 0. For cases of lupus nephritis, a complete response was defined as a proteinuria of < 500 mg/24h and an eGFR 60 ml/min; a partial response was defined as a reduction of the proteinuria of > 50% of baseline values and an eGFR 60 ml/min. In cases of lung involvement, a response was defined as an FVC decline £ 5% predicted values. Results RTX was administered in 62 patients with SLE treated at the 2 Rheumatology tertiary care centers of southwestern Greece. For this cross-sectional study we enrolled 23 patients (25 cases) with SLE (all Caucasian female, age range: 14 – 72yr, mean: 31yr) with active or relapsing disease, fulfilling inclusion criteria. The median disease duration was 6yr (range: 2mo-27yr) at the time of the first RTX treatment infusion. Clinical manifestations at the time of RTX introduction included lupus nephritis in 8 patients, arthritis in 6, neuropsychiatric involvement in 4, vasculitis in 2, lung involvement in 3 and hematological abnormalities in 3. RTX was also administered in 1 patient with lupus hepatitis and in 1 plasmapheresis-plus-steroid resistant case of thrombotic thrombopenic purpura. RTX treatment was associated with a clinical benefit in 82.14% of our patients after 1yr and in 74.48% after ³10yr. The median cSLEDAI-2K score decreased from 5.83 ± 3.70 at baseline to 1.95 ± 2.40 (p < 0.001) at 1yr and to 2.37 ± 3.00 (p < 0.001) at the ³10yr timepoint of follow-up. Ten out of our 23 patients relapsed. The earliest relapse was seen at 6mo and the latest at 13yr after RTX treatment introduction. Eight relapsed patients were re-treated with RTX and 3/8 re-responded. The mean daily dose of corticosteroids was reduced both at the 1yr and at the ³ 10yr time points; dose reductions were not statistically significant. Regarding safety we report 1 COVID19-related death, viral infections in 2, allergic reactions in 4 and 1 patient with late-onset neutropenia. Conclusions Our data suggest that RTX may indeed represent an alternative therapeutic option in patients with SLE refractory to standard treatment with an acceptable safety profile and a potential long-term beneficial effect.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.006

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0010.001
Open science0.0000.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0010.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.008
GPT teacher head0.262
Teacher spread0.254 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

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