Evidence map›Paper›PMID 39037917›Full record

ArticleRheumatology (Oxford, England)2025

Preventive effects of early immunosuppressive treatment on the development of interstitial lung disease in systemic sclerosis.

Arthiha Velauthapillai, M F R Bootsma, Cosimo Bruni, Christina Bergmann, Marco Matucci-Cerinic, David Launay, Gabriela Riemekasten, L Garzanova, Paolo Airò, Elena Rezus and 9 more

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Treating connective tissue disease-associated interstitial lung disease - think outside the box: a perspective.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Arthiha VelauthapillaiDepartment of Rheumatology, Radboud University Medical Center, Nijmegen, Netherlands.ORCID 0009-0006-0700-7573
M F R BootsmaDepartment of Rheumatology, Radboud University Medical Center, Nijmegen, Netherlands.ORCID 0009-0005-1724-1112
Cosimo BruniDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0003-2813-2083
Christina BergmannDepartment of Internal Medicine 3, Rheumatology and Clinical Immunology, Friedrich-Alexander-University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.ORCID 0000-0001-5257-9171
Marco Matucci-CerinicUniversity Vita Salute San Raffaele, Milano, Italy.ORCID 0000-0002-9324-3161
David LaunayDépartement de Médecine Interne et d'Immunologie Clinique, Centre National de Référence Maladies Systémiques et Auto-immunes Rares Nord et Nord-Ouest de France (CeRAINO), European Reference Network on Rare Connective Tissue and Musculoskeletal Diseases Network (ReCONNECT), Univ. Lille, CHU Lille, Lille, France.ORCID 0000-0003-1840-1817
Gabriela RiemekastenDepartment of Rheumatology and Clinical Immunology, University of Medical Center Schleswig-Holstein, University Lübeck, Germany.ORCID 0000-0002-5406-2464
L GarzanovaVA Nasonova Research Institute of Rheumatology, Moscow, Russian Federation.ORCID 0000-0002-5012-0540
Paolo AiròUOC Reumatologia e Immunologia Clinica, ASST Spedali Civili di Brescia, Brescia, Italy.ORCID 0000-0001-5241-1918
Elena RezusDepartment of Rheumatology, 'Grigore T. Popa' University of Medicine and Pharmacy, 16 Universitatii Street, Iasi, Romania.ORCID 0000-0002-8175-2583
Jose A P da SilvaFaculty of Medicine, University of Coimbra, Coimbra, Portugal.ORCID 0000-0002-2782-6780
Francesco Del GaldoLeeds Raynaud's And Scleroderma Program, NIHR Biomedical Research Centre Leeds Institute Of Rheumatic And Musculoskeletal Medicine, University of Leeds, Leeds, UK.ORCID 0000-0002-8528-2283
Nicolas HunzelmannDepartment of Dermatology, University of Cologne, Köln, Germany.
Lorinda S ChungDepartment of Medicine & Dermatology, Division of Immunology & Rheumatology, Stanford University School of Medicine and Palo Alto VA Health Care System, Palo Alto, CA, USA.ORCID 0000-0003-0072-6939
Dorota KrasowskaDepartment of Dermatology, Venereology and Pediatric Dermatology, Medical University of Lublin, Lublin, Poland.ORCID 0000-0002-3176-9870
Oliver DistlerDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-0546-8310
Cornelia H M van den EndeDepartment of Rheumatology, Radboud University Medical Center, Nijmegen, Netherlands.ORCID 0000-0002-4352-2824
Madelon C VonkDepartment of Rheumatology, Radboud University Medical Center, Nijmegen, Netherlands.ORCID 0000-0002-2266-9907
EUSTAR Collaborators

Funding

Foundation for Research in RheumatologyScleroderma Clinical Trials ConsortiumScleroderma Research FoundationWellcome Trust
6 · The paper itself

Abstract

backgroundHypothesizing that early treatment yields improved prognosis, we aimed to investigate how the timing of immunosuppressive treatment relates to interstitial lung disease (ILD) development and the course of pulmonary function in systemic sclerosis (SSc).

methodsA cohort was created using data from the EUSTAR database and Nijmegen Systemic Sclerosis cohort, including adult patients who started their first immunosuppressive treatment (i.e. mycophenolate mofetil, methotrexate, cyclophosphamide, tocilizumab or rituximab) after SSc diagnosis, and no signs of ILD on high-resolution CT. ILD-free survival and the course of forced vital capacity (FVC) % predicted were assessed for up to 5 years' follow-up comparing patients who started early (disease duration ≤3 years) vs late with immunosuppression.

results1052 patients met the eligibility criteria. The early treatment group (n = 547, 52%) showed a higher prevalence of male sex, diffuse cutaneous subtype (53.1% vs 36.5%), and anti-topoisomerase-I antibody (ATA, 51.1% vs 42.7%). Most patients were treated with methotrexate (60.1%), whereas only a few patients were treated with biologics (1.7%). The incidence of ILD was 46.6% after mean (s.d.) 3.6 (1.4) years; the hazards ratio for ILD in the early treatment group was 1.13 (95% CI: 0.93, 1.38) after adjustment for confounders. FVC % predicted trajectories were comparable between groups.

conclusionOur findings did not confirm a preventive role of early initiation of immunosuppressive therapy vs late initiation on ILD development. However, our findings should be interpreted with caution, considering the high inflammatory, ATA-positive enriched nature of the cohort, confounding by indication, and that very few patients were treated with biologics.

Indexed as

Immunosuppressive AgentsLung Diseases, InterstitialScleroderma, SystemicAdultAgedFemaleHumansMaleMethotrexateMiddle AgedMycophenolic AcidVital CapacityImmunosuppressive AgentsMethotrexateMycophenolic Acidearly treatmentinterstitial lung diseasesystemic sclerosis

Identifiers

PMID39037917
PMCPMC12695046

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Registered trials

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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.