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

Authors :
Alain Lescoat
Francesco Del Galdo
Peter A. Merkel
Dominique Godard
Michael Hughes
Sue Farrington
Susan L. Murphy
Virginia D. Steen
David Cella
John D Pauling
Dinesh Khanna
Rachel Wessel
Yannick Allanore
Christopher P. Denton
Robert D Sandler
David Roofeh
François Zimmermann
Lorinda Chung
Maya H. Buch
Whitney Townsend
Chard-Hutchinson, Xavier
Institut de recherche en santé, environnement et travail (Irset)
Université d'Angers (UA)-Université de Rennes (UR)-École des Hautes Études en Santé Publique [EHESP] (EHESP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )
CHU Pontchaillou [Rennes]
University of Michigan [Ann Arbor]
University of Michigan System
Royal United Hospitals Bath (RUH)
School of Veterinary and Life Sciences [Murdoch]
Murdoch University
Sheffield Children's NHS Foundation Trust
Stanford University
University College London Hospitals (UCLH)
Hospital of the University of Pennsylvania (HUP)
Perelman School of Medicine
University of Pennsylvania-University of Pennsylvania
Georgetown University Medical Center
Hôpital Cochin [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
University of Leeds
Association des Sclérodermie de France
Northwestern University Feinberg School of Medicine
Manchester Academic Health Science Centre (MAHSC)
University of Manchester [Manchester]
SRUK/WSF [UHUHR1]
NIH/NIAMS 24 [AR063120]
Y NIH/NIAMS T32 grant [AR007080]
Université d'Angers (UA)-Université de Rennes 1 (UR1)
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-École des Hautes Études en Santé Publique [EHESP] (EHESP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )
University of Pennsylvania [Philadelphia]-University of Pennsylvania [Philadelphia]
Source :
Journal of Scleroderma and Related Disorders, Journal of Scleroderma and Related Disorders, 2021, 6 (1), pp.66-76. ⟨10.1177/2397198320961967⟩, J Scleroderma Relat Disord
Publication Year :
2020
Publisher :
SAGE Publications, 2020.

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.

Details

ISSN :
23971991 and 23971983
Volume :
6
Database :
OpenAIRE
Journal :
Journal of Scleroderma and Related Disorders
Accession number :
edsair.doi.dedup.....427662109927fd30c5af58fc49b4dc13
Full Text :
https://doi.org/10.1177/2397198320961967