4.7 Article

New composite endpoint in early diffuse cutaneous systemic sclerosis: revisiting the provisional American College of Rheumatology Composite Response Index in Systemic Sclerosis

Journal

ANNALS OF THE RHEUMATIC DISEASES
Volume 80, Issue 5, Pages 641-650

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/annrheumdis-2020-219100

Keywords

scleroderma; systemic; outcome assessment; health care; patient reported outcome measures

Categories

Funding

  1. NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases [K24-AR-063120, 1R01-AR070470-01A1]

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The ACR-CRISS is a composite endpoint for diffuse systemic sclerosis, consisting of five core measures. By analyzing data from multiple trials, researchers found that a revised version of the CRISS, based on certain percentage improvements in core measures, could be a potential new outcome measure.
Objectives American College of Rheumatology Composite Response Index in Systemic Sclerosis (ACR-CRISS) is a composite endpoint to assess the likelihood of improvement in diffuse systemic sclerosis. ACR-CRISS is a weighted score and includes five core set measures: modified Rodnan skin score, FVC% predicted, health assessment questionnaire-disability index, and patient and clinician global assessments. Methods We analysed core set measures from 354 participants who participated in three placebo-controlled trials. We generated 10 development datasets, randomly selected from 2/3 of the participants, stratified by study and treatment group. The remaining participants (1/3 of the participants) formed the validation sets. Risk differences (RDs) between active and placebo treatments were calculated by averaging over the replicate datasets; bootstrap 95% CIs for the RDs to estimate the magnitude of treatment effects. Results In the development sets (n=237), the proportion of participants in the active group had statistically higher improvement in >1 of 5 core set measures versus the placebo group. For example, the proportion who improved by >= 20% in >= 3 core set measures was 49.4% in the active versus338.9% in the placebo; RD: 10.5%, 95% CI4.9 % to 16.1%. In the validation sets (n=117), the proportion who improved by >= 20% in >= 3 core set measures was 50.3% in the active versus35.63% in the placebo (RD:114.8%, 95% CI 3.1% to225.7%). Similar trends were seen with larger percentage cut-offs. Conclusion Revised CRISS, as assessed by the proportion of participants who improved by a certain percentage in >= 3 of 5 core set measures, is a potential new composite outcome measure.

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