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Alternative Ways to Quantify Sustained Remission: Applying the Continuity Rewarded Score and Patient Vector Graph
Maud S Jurgens1, Johannes W G Jacobs1, Maarten Boers2
1University Medical Center Utrecht, Utrecht, The Netherlands.
New scoring methods, the Continuity Rewarded (ConRew) score and a simple sum score, along with patient vector graphs, effectively revealed greater remission in early rheumatoid arthritis patients treated with methotrexate plus prednisone compared to placebo.
Area of Science:
- Rheumatology
- Clinical Trial Analysis
- Statistical Methods in Medicine
Background:
- The Computer Assisted Management in Early Rheumatoid Arthritis Trial-II (CAMERA-II) indicated clinical benefits of methotrexate (MTX) plus prednisone over MTX with placebo.
- However, the difference in remission rates was only significant in one of three analyses, suggesting limitations in conventional assessment methods.
Purpose of the Study:
- To evaluate if the Continuity Rewarded (ConRew) score and a simple sum score could better differentiate remission between treatment arms in CAMERA-II.
- To assess the added value of patient vector graphs in visualizing remission data compared to standard box plots.
Main Methods:
- The ConRew score, which prioritizes continuous remission periods, was applied alongside a simple sum score of 4-week remission periods.
- Patient vector graphs were utilized and compared against conventional group-level box plots.
Main Results:
- Both the simple sum score and ConRew score demonstrated significantly higher (more favorable) remission in the MTX + prednisone group compared to the MTX + placebo group (P=0.003 and P=0.004, respectively).
- Patient vector graphs visually depicted more frequent and longer remission periods in the MTX + prednisone group, offering additional insights beyond box plots.
Conclusions:
- The simple sum score, ConRew score, and patient vector graphs enhance the understanding and discriminatory power in analyzing remission outcomes in early rheumatoid arthritis.
- These methods provide a more nuanced assessment of treatment efficacy in clinical trials.
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