Considerations for a combined index for limited cutaneous systemic sclerosis to support drug development and improve outcomes

Author:

Lescoat Alain12ORCID,Murphy Susan L34,Roofeh David5ORCID,Pauling John D6ORCID,Hughes Michael7,Sandler Robert7ORCID,Zimmermann François2ORCID,Wessel Rachel5ORCID,Townsend Whitney8,Chung Lorinda910,Denton Christopher P11ORCID,Merkel Peter A1213,Steen Virginia14,Allanore Yannick15,Del Galdo Francesco16ORCID,Godard Dominique17,Cella David18,Farrington Sue19,Buch Maya H2021,Khanna Dinesh5

Affiliation:

1. Univ Rennes, CHU Rennes, Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement et Travail)—UMR_S 1085, Rennes, France

2. Department of Internal Medicine and Clinical Immunology, Rennes University Hospital, Rennes, France

3. Department of Physical Medicine and Rehabilitation, University of Michigan, Ann Arbor, MI, USA

4. VA Ann Arbor Healthcare System, GRECC, Ann Arbor, MI, USA

5. Scleroderma Program, Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA

6. Royal National Hospital for Rheumatic Diseases (at Royal United Hospitals), Bath, UK

7. Department of Rheumatology, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK

8. Taubman Health Sciences Library, University of Michigan, Ann Arbor, MI, USA

9. Division of Immunology and Rheumatology, Stanford University School of Medicine, Palo Alto, CA, USA

10. Division of Immunology and Rheumatology, VA Palo Alto Health Care System, Palo Alto, CA, USA

11. Centre for Rheumatology and Connective Tissue Diseases, Royal Free Hospital Campus, University College London Medical School, London, UK

12. Division of Rheumatology, Department of Medicine, University of Pennsylvania, Philadelphia, PA, USA

13. Division of Clinical Epidemiology, Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania, Philadelphia, PA, USA

14. Division of Rheumatology, Georgetown University Medical Center, Washington, DC, USA

15. Department of Rheumatology, Cochin Hospital, AP-HP, Paris Descartes University, Paris, France

16. Institute of Rheumatic and Musculoskeletal Medicine and NIHR Biomedical Research Centre, University of Leeds, Leeds, UK

17. Association des Sclérodermie de France, Auxerre, France

18. Department of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, USA

19. Federation of European Scleroderma Associations (FESCA), Tournai, Belgium

20. Centre for Musculoskeletal Research, School of Biological Sciences, Faculty of Biology, Medicine & Health, University of Manchester, Manchester, UK

21. NIHR Manchester Biomedical Research Centre, Manchester Academic Health Science Centre, Manchester University Foundation Trust, Manchester, UK

Abstract

Systemic sclerosis (systemic scleroderma) is characterized by a heterogeneous range of clinical manifestations. Systemic sclerosis is classified into limited cutaneous systemic sclerosis and diffuse cutaneous systemic sclerosis subgroups based on the extent of skin involvement. Randomized controlled trials in scleroderma have mainly focused on diffuse cutaneous systemic sclerosis partly because the measurement of skin involvement, critical for evaluating a therapeutic intervention, is more dynamic in this subset. Nonetheless, limited cutaneous systemic sclerosis, the most common cutaneous subset (about two-third), is also associated with significant morbidity and detrimental impact on health-related quality of life. The lack of interventional studies in limited cutaneous systemic sclerosis is partly due to a lack of relevant outcome measures to evaluate this subgroup. Combining several clinically meaningful outcomes selected specifically for limited cutaneous systemic sclerosis may improve representativeness in clinical trials and responsiveness of outcomes measured in randomized controlled trials. A composite index dedicated to limited cutaneous systemic sclerosis combining such relevant outcomes could advance clinical trial development for limited cutaneous systemic sclerosis by providing the opportunity to test and select among candidate drugs that could act as disease-modifying treatments for this neglected subgroup of systemic sclerosis. This proposed index would include items selected by expert physicians and patients with limited cutaneous systemic sclerosis across domains grounded in the lived experience of limited cutaneous systemic sclerosis. This article reviews the reasons behind the relative neglect of limited cutaneous systemic sclerosis, discusses the current state of outcome measures for limited cutaneous systemic sclerosis, identifies challenges, and proposes a roadmap for a combined limited cutaneous systemic sclerosis-specific treatment response index.

Funder

SRUK/WSF

NIH/NIAMS

NIH/NIAMS T32 grant

Publisher

SAGE Publications

Subject

Immunology,Rheumatology,Immunology and Allergy

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