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Research ArticleArticle

A Systematic Review of Clinical Trial Designs and Outcome Measures in Sjögren Disease Randomized Controlled Trials

Maxime Beydon, Yann Nguyen, Rachael Gordon, Nathan Foulquier, Coralie Bouillot, Katherine M. Hammitt, Simon J. Bowman, Xavier Mariette, Divi Cornec, Sara S. McCoy and Raphaèle Seror
The Journal of Rheumatology April 2025, jrheum.2024-1012; DOI: https://doi.org/10.3899/jrheum.2024-1012
Maxime Beydon
M. Beydon, MD, MPH, Service de Rhumatologie, AP-HP, Hôpital Bicêtre, Le Kremlin Bicêtre, and Service de Médecine Interne, Hôpital Beaujon, AP-HP Nord, Université Paris Cité, Clichy, France.
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Yann Nguyen
Y. Nguyen, MD, PhD, Service de Médecine Interne, Hôpital Beaujon, AP-HP Nord, Université Paris Cité, Clichy, and Center for Immunology of Viral Infections and Auto-immune Diseases (IMVA), INSERM, UMR 1184, Université Paris-Saclay, Le Kremlin Bicêtre, Paris, France.
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Rachael Gordon
R. Gordon, MD, PhD, Department of Medicine, Division of Rheumatology and Clinical Immunology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
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Nathan Foulquier
N. Foulquier, PhD, INSERM 1227, B Lymphocytes, Autoimmunity and Immunotherapies (LBAI), Université de Bretagne Occidentale, Brest, France.
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Coralie Bouillot
C. Bouillot, Sjögren Europe, Bienne, Switzerland.
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Katherine M. Hammitt
K.M. Hammitt, Sjögren's Foundation, Bethesda, Maryland, USA.
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Simon J. Bowman
S.J. Bowman, MD, PhD, Rheumatology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
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Xavier Mariette
X. Mariette, MD, PhD, Service de Rhumatologie, AP-HPs, Hôpital Bicêtre, Le Kremlin Bicêtre, and Center for Immunology of Viral Infections and Auto-immune Diseases (IMVA), INSERM, UMR 1184, Université Paris-Saclay, Le Kremlin Bicêtre, Paris, France.
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Divi Cornec
D. Cornec, MD, PhD, INSERM 1227, B Lymphocytes, Autoimmunity and Immunotherapies (LBAI), Université de Bretagne Occidentale, Brest, France.
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Sara S. McCoy
S.S. McCoy, MD, PhD, Division of Rheumatology, Department of Medicine, School of Medicine and Public Health, University of Wisconsin, Madison, Wisconsin, USA.
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Raphaèle Seror
R. Seror, MD, PhD, Service de Rhumatologie, AP-HPs, Hôpital Bicêtre, Le Kremlin Bicêtre, and Center for Immunology of Viral Infections and Auto-immune Diseases (IMVA), INSERM, UMR 1184, Université Paris-Saclay, Le Kremlin Bicêtre, Paris, France.
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Abstract

Objective To systematically review all existing Sjögren disease (SjD)-related instruments reported in clinical trials for SjD.

Methods We systematically searched Medline (PubMed) and EMBASE between January 2002 and March 2023 to identify all randomized controlled trials (RCTs) using both a manual approach and artificial intelligence software (Bibliography BOT). We extracted all the instruments used as primary or secondary outcomes and assessed whether the study succeeded in improving the outcome. We also classified the instruments according to the recently defined preliminary outcome domains.

Results Among 5420 references, 60 RCTs were included, focusing either on overall disease manifestations (53%) or on a single organ/symptom (eg, dry eyes [17%], xerostomia [15%], fatigue [12%], or pulmonary function [3%]). Primary outcomes included measures of oral or ocular dryness, patient-reported outcomes (PROs), systemic activity, and other outcomes. Common instruments used were European Alliance of Associations for Rheumatology (EULAR) Sjögren Syndrome Disease Activity Index (ESSDAI), EULAR Sjögren Syndrome Patient-Reported Index, Schirmer-I test for unstimulated salivary flow, and IgG levels. ESSDAI was a primary outcome in 11 studies, with 45% of studies reaching significance, whereas none of the 16 studies with ESSDAI as a secondary outcome reached significance. PROs were the primary outcome in 34 studies. Glandular function measurements varied, with unstimulated salivary flow as the most commonly measured outcome. Life impact was assessed more frequently as a secondary outcome. Only 2 studies focused on biological activity.

Conclusion Our review highlighted the heterogeneity of SjD RCTs in both the study designs and outcomes. The use of PROs and composite outcomes has increased in recent years, highlighting a shift from objective dryness measures to more holistic patient-centered outcomes.

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The Journal of Rheumatology: 53 (1)
The Journal of Rheumatology
Vol. 53, Issue 1
1 Jan 2026
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A Systematic Review of Clinical Trial Designs and Outcome Measures in Sjögren Disease Randomized Controlled Trials
Maxime Beydon, Yann Nguyen, Rachael Gordon, Nathan Foulquier, Coralie Bouillot, Katherine M. Hammitt, Simon J. Bowman, Xavier Mariette, Divi Cornec, Sara S. McCoy, Raphaèle Seror
The Journal of Rheumatology Apr 2025, jrheum.2024-1012; DOI: 10.3899/jrheum.2024-1012

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A Systematic Review of Clinical Trial Designs and Outcome Measures in Sjögren Disease Randomized Controlled Trials
Maxime Beydon, Yann Nguyen, Rachael Gordon, Nathan Foulquier, Coralie Bouillot, Katherine M. Hammitt, Simon J. Bowman, Xavier Mariette, Divi Cornec, Sara S. McCoy, Raphaèle Seror
The Journal of Rheumatology Apr 2025, jrheum.2024-1012; DOI: 10.3899/jrheum.2024-1012
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