Evidence map›Paper›PMID 42832020›Full record

ArticleClinical rheumatology2026

Real-world outcomes after anifrolumab initiation in systemic lupus erythematosus: a pragmatic treat-to-target analysis.

Dalifer Freites Núñez, Paloma Camarero Diaz, Sara Rodríguez Montes, Cristina Martínez Prada, Cristina Lajas Petisco, Lydia Abasolo, Benjamin Fernández Gutierrez

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Article in Clinical rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Dalifer Freites NúñezRheumatology Department, Hospital Universitario Clínico San Carlos, Prof. Martín Lagos s/n, 28040, Madrid, Spain. daliferdayanira.freites@salud.madrid.org.ORCID http://orcid.org/0000-0002-0966-2778
Paloma Camarero DiazRheumatology Department, Hospital Universitario Clínico San Carlos, Prof. Martín Lagos s/n, 28040, Madrid, Spain.
Sara Rodríguez MontesRheumatology Department, Hospital Universitario Clínico San Carlos, Prof. Martín Lagos s/n, 28040, Madrid, Spain.
Cristina Martínez PradaRheumatology Department, Hospital Universitario Clínico San Carlos, Prof. Martín Lagos s/n, 28040, Madrid, Spain.
Cristina Lajas PetiscoRheumatology Department, Hospital Universitario Clínico San Carlos, Prof. Martín Lagos s/n, 28040, Madrid, Spain.
Lydia AbasoloGrupo de Patología Musculoesquelética, Instituto de Investigación Sanitaria San Carlos (IdISSC), Madrid, Spain.
Benjamin Fernández GutierrezRheumatology Department, Hospital Universitario Clínico San Carlos, Prof. Martín Lagos s/n, 28040, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

INTRODUCTION/

objectivesTreat-to-target (T2T) strategies in systemic lupus erythematosus (SLE) emphasise remission or low disease activity together with glucocorticoid minimisation. Real-world evidence evaluating anifrolumab using predefined target-oriented outcomes remains limited. We evaluated outcomes after anifrolumab initiation within a pragmatic T2T framework.

methodsThis retrospective single-centre cohort included adults with SLE receiving anifrolumab. The study-defined pragmatic low disease activity composite required SLEDAI-2K ≤ 4, Physician Global Assessment ≤ 1, prednisone ≤ 7.5 mg/day, and absence of clinically significant renal activity. Prednisone ≤ 5 mg/day was explored in sensitivity analyses. Outcomes were assessed at baseline and 1, 3, 6, and 12 months. Longitudinal changes in SLEDAI-2K, PGA, and prednisone dose were analysed using linear mixed-effects models.

resultsNineteen patients were included (median baseline SLEDAI-2K 12.0 and median PGA 2.0). Composite attainment using prednisone ≤ 7.5 mg/day was 5.3% at 1 month, 47.4% at 3 months, 50.0% at 6 months, and 8/12 (66.7%) at 12 months. Using prednisone ≤ 5 mg/day, attainment was 36.8% at 3 months, 50.0% at 6 months, and 66.7% at 12 months. Disease activity components were met earlier than glucocorticoid thresholds. Mixed-effects models showed significant reductions in SLEDAI-2K, PGA, and prednisone dose during follow-up. One patient permanently discontinued anifrolumab due to influenza A, and one temporarily interrupted treatment because of pneumonia.

conclusionsAfter anifrolumab initiation, the proportion of evaluable patients meeting the pragmatic composite increased alongside reductions in disease activity and glucocorticoid dose. These exploratory findings suggest a potential role for anifrolumab within T2T strategies and warrant confirmation in larger controlled studies using validated treatment targets.

Indexed as

AnifrolumabGlucocorticoidsLow disease activityLupus erythematosus, systemicReal-world evidenceTreat-to-target

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.