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Extended report
Development of a provisional core set of response measures for clinical trials of systemic sclerosis
  1. D Khanna1,
  2. D J Lovell2,
  3. E Giannini2,
  4. P J Clements1,
  5. P A Merkel3,
  6. J R Seibold4,
  7. M Matucci-Cerinic5,
  8. C P Denton6,
  9. M D Mayes7,
  10. V D Steen8,
  11. J Varga9,
  12. D E Furst1,
  13. for the Scleroderma Clinical Trials Consortium co-authors
  1. 1
    Division of Rheumatology, Department of Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, USA
  2. 2
    Division of Rheumatology, Cincinnati Children’s Medical Center, Cincinnati, Ohio, USA
  3. 3
    Section of Rheumatology and the Clinical Epidemiology Unit, Boston University School of Medicine, Boston, Massachusetts, USA
  4. 4
    University of Michigan Scleroderma Program, Ann Arbor, Michigan, USA
  5. 5
    University of Florence, Florence, Italy
  6. 6
    Royal Free Hospital, London, UK
  7. 7
    Division of Rheumatology and Clinical Immunogenetics, The University of Texas Houston Medical School, Houston, Texas, USA
  8. 8
    Division of Rheumatology, Georgetown University Medical Center, Washington DC, USA
  9. 9
    Division of Rheumatology, Northwestern University Medical School, Chicago, Illinois, USA
  1. D Khanna, Division of Rheumatology, Department of Medicine, David Geffen School of Medicine, 1000 Veterans Avenue, Rm 32-59 Rehabilitation Building, Los Angeles, California 90095, USA; dkhanna{at}mednet.ucla.edu

Abstract

Objective: To develop a provisional core set of response measures for clinical trials of systemic sclerosis (SSc).

Methods: The Scleroderma Clinical Trials Consortium (SCTC) conducted a structured, 3-round Delphi exercise to reach consensus on a core set of measures for clinical trials of SSc. Round 1 asked the SCTC investigators to list items in 11 pre-defined domains (skin, musculoskeletal, cardiac, pulmonary, cardio-pulmonary, gastrointestinal, renal, Raynaud phenomenon and digital ulcers, health-related quality of life and function, global health, and biomarkers) for SSc clinical trials. Round 2 asked respondents to rate the importance of the chosen items and was followed by a meeting, during which the Steering Committee discussed the feasibility, reliability, redundancy and validity of the items. Round 3 sought to obtain broader consensus on the core set measures. Members also voted on items that had data on feasibility but lacked data on reliability and validity, but may still be useful research outcome measures for future trials.

Results: A total of 50 SCTC investigators participated in round 1, providing 212 unique items for the 11 domains. In all, 46 (92%) participants responded in round 2 and rated 177 items. The ratings of 177 items were reviewed by the Steering Committee and 31 items from the 11 domains were judged to be appropriate for inclusion in a 1-year multi-centre clinical trial. In total, 40 SCTC investigators completed round 3 and ranked 30 of 31 items as acceptable for inclusion in the core set. The Steering Committee also proposed 14 items for a research agenda.

Conclusion: Using a Delphi exercise, we have developed a provisional core set of measures for assessment of disease activity and severity in clinical trials of SSc.

https://doi.org/10.1136/ard.2007.078923

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    Footnotes

    • Funding: This project was funded by a National Institutes of Health Award (NIAMS U01 AR055057-01). DK was supported by the Scleroderma Foundation (New Investigator Award), a National Institutes of Health Award (NIAMS K23 AR053858-01A1), and a grant from the Scleroderma Clinical Trial Consortium. PAM is supported by a Mid-Career Clinical Investigator Award (NIAMS K24 AR2224-01A1).

    • Competing interests: None declared.