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Comparison of Evans syndrome and isolated autoimmune cytopenias in SLE: a retrospective study

Title: Comparison of Evans syndrome and isolated autoimmune cytopenias in SLE: a retrospective study
Authors: El-Jammal, Thomas; Fabre-Barthez, Anne; Martinet, Nicolas; Roussotte, Mickaël; Hot, Arnaud; Baudet, Antoine; Reynaud, Quitterie; Durieu, Isabelle; Pérard, Laurent; Barba, Thomas; Sève, Pascal
Source: Lupus Science & Medicine ; volume 13, issue 1, page e001866 ; ISSN 2053-8790
Publisher Information: BMJ
Publication Year: 2026
Description: Objective To compare patients with SLE associated with either Evans syndrome (ES) or an isolated autoimmune cytopenia (immune thrombocytopenia (ITP) or autoimmune haemolytic anaemia (AIHA)). Methods Multicentre retrospective study including patients with SLE presenting with ITP, AIHA or ES of clinical significance (ie, requiring therapeutic intervention according to European Alliance of Associations for Rheumatology guidelines or clinician discretion). Clinical, laboratory and outcome data were compared between patients with ES and those with ITP or AIHA. Severe SLE flares were defined as flares with SLE Disease Activity Index ≥10. Results Among 95 patients with SLE included, 30 had ES, 43 ITP and 22 AIHA. The number of severe SLE flares per patient was higher in ES than in ITP (1.3 vs 0.4, p=0.0004) and patients with AIHA (0.4, p=0.006). Patients with ES had a higher incidence rate ratio (IRR) of severe SLE flares (IRR =3.03; 95% CI 1.50 to 6.41), which remained significant in inverse probability of treatment weighting analyses. At last follow-up, patients with ES presented higher rates of renal (36.7% vs 9.3%, p=0.007) and neurological (36.7% vs 11.6%, p=0.019) involvement than patients with ITP. Severe infections were more frequent in patients with ES than ITP (47% vs 23%, p=0.045), with a higher mean number of severe infections per patient (1.2 vs 0.5, p=0.04). Conclusion In patients with SLE, ES is associated with an increased risk of severe flares than isolated autoimmune cytopenia. These findings were consistent after adjustment for baseline imbalances, supporting ES as a high-risk SLE phenotype.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1136/lupus-2025-001866
Availability: https://doi.org/10.1136/lupus-2025-001866; https://syndication.highwire.org/content/doi/10.1136/lupus-2025-001866
Rights: https://creativecommons.org/licenses/by-nc/4.0/
Accession Number: edsbas.81A7E810
Database: BASE