Lewis James D, Chuai Shaokun, Nessel Lisa, Lichtenstein Gary R, Aberra Faten N, Ellenberg Jonas H
Division of Gastroenterology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6021, USA.
Inflamm Bowel Dis. 2008 Dec;14(12):1660-6. doi: 10.1002/ibd.20520.
The Mayo score and a noninvasive 9-point partial Mayo score are used as outcome measures for clinical trials assessing therapy for ulcerative colitis (UC). There are limited data assessing what defines a clinically relevant change in these indices. We sought to assess what constitutes a clinically meaningful change in these indices using data from a recently completed placebo-controlled clinical trial.
In all, 105 patients were enrolled in a 12-week randomized, placebo-controlled trial assessing rosiglitazone for treatment of mild to moderate UC. We compared the change in the Mayo score, the partial Mayo score, and a 6-point score composed just of the stool frequency and bleeding components of the Mayo score to the patient's perception of disease activity at week 0 and week 12. Optimal cutpoints were calculated as the maximal product of sensitivity and specificity.
Each index was strongly correlated with the patient's rating of disease activity at week 12 (Spearman correlations 0.61-0.71, P < 0.0001 for all correlations). The maximal product of sensitivity and specificity to identify patient reported improvement of disease activity was achieved using cutpoints for change of 2.5 for the Mayo score (sensitivity 88%, specificity 80%), 2.5 for the partial Mayo score (sensitivity 88%, specificity 87%), and 1.5 for the 6-point score (sensitivity 88%, specificity 80%).
The partial Mayo score and the 6-point score composed solely of the stool frequency and bleeding components performed as well as the full Mayo score to identify patient perceived clinical response.
梅奥评分和无创9分部分梅奥评分被用作评估溃疡性结肠炎(UC)治疗效果的临床试验的结局指标。评估这些指标中具有临床意义的变化的定义的数据有限。我们试图利用最近完成的一项安慰剂对照临床试验的数据,评估这些指标中构成临床有意义变化的因素。
总共105例患者参加了一项为期12周的随机、安慰剂对照试验,该试验评估罗格列酮治疗轻至中度UC的效果。我们将梅奥评分、部分梅奥评分以及仅由梅奥评分中的大便频率和出血成分组成的6分评分的变化与患者在第0周和第12周对疾病活动的感知进行了比较。最佳切点计算为敏感性和特异性的最大乘积。
每个指标与患者在第12周对疾病活动的评分密切相关(Spearman相关性为0.61 - 0.71,所有相关性的P < 0.0001)。使用梅奥评分变化2.5(敏感性88%,特异性80%)、部分梅奥评分变化2.5(敏感性88% ,特异性87%)以及6分评分变化1.5(敏感性88%,特异性80%)的切点,可实现识别患者报告疾病活动改善的敏感性和特异性的最大乘积。
部分梅奥评分以及仅由大便频率和出血成分组成的6分评分在识别患者感知的临床反应方面与完整的梅奥评分表现相当。