Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
Inflammatory Bowel Disease Unit, Department of Medicine, University of Calgary, AB, Canada.
Inflamm Bowel Dis. 2020 Sep 18;26(10):1562-1571. doi: 10.1093/ibd/izaa025.
CALM was a randomized phase 3 trial in patients with Crohn's disease (CD) that demonstrated improved endoscopic outcomes when treatment was escalated based on cutoffs for inflammatory biomarkers, fecal calprotectin (FC), C-reactive protein (CRP), and CD Activity Index (CDAI) remission vs CDAI response alone. The purpose of this post hoc analysis of CALM was to identify drivers of treatment escalation and evaluate the association between biomarker cutoff concentrations and endoscopic end points.
The proportion of patients achieving CD Endoscopic Index of Severity (CDEIS) <4 and no deep ulcers 48 weeks after randomization was evaluated according to CRP <5 mg/L or ≥5 mg/L and FC <250 μg/g or ≥250 μg/g. Subgroup analyses were performed according to disease location, and sensitivity analyses were conducted in patients with elevated CRP and/or FC at baseline. The association between endoscopic end points and biomarker cutoffs was performed using χ 2 test.
The proportion of patients who achieved the primary end point CDEIS <4 and no deep ulcers was significantly greater for those with FC <250 µg/g (74%; P < 0.001), with an additive effect for CRP <5 mg/L. The association of FC <250 µg/g with improved endoscopic outcomes was independent of disease location, although the greatest association was observed for ileocolonic disease. Fecal calprotectin <250 µg/g, CRP <5 mg/L, and CDAI <150 gave a sensitivity/specificity of 72%/63% and positive/negative predictive values of 86%/42% for CDEIS <4 and no deep ulcers 48 weeks after randomization.
This post hoc analysis of CALM demonstrated that a cutoff of FC <250 µg/g is a useful surrogate marker for mucosal healing in CD.
CALM 是一项针对克罗恩病(CD)患者的随机 3 期试验,结果表明,根据炎症生物标志物、粪便钙卫蛋白(FC)、C 反应蛋白(CRP)和 CD 活动指数(CDAI)缓解与 CDAI 反应的截止值来升级治疗时,内镜结局得到改善。本 CALM 的事后分析旨在确定治疗升级的驱动因素,并评估生物标志物截止值浓度与内镜终点之间的关系。
根据 CRP<5 mg/L 或≥5 mg/L 和 FC<250 μg/g 或≥250 μg/g,评估随机分组后 48 周时 CD 内镜严重程度指数(CDEIS)<4 和无深溃疡的患者比例。根据疾病部位进行亚组分析,并对基线时 CRP 和/或 FC 升高的患者进行敏感性分析。使用 χ²检验评估内镜终点与生物标志物截止值之间的关系。
FC<250 μg/g 的患者达到主要终点 CDEIS<4 和无深溃疡的比例显著更高(74%;P<0.001),且 CRP<5 mg/L 有附加效应。FC<250 μg/g 与改善的内镜结局相关,与疾病部位无关,但在回肠-结肠疾病中观察到最大的相关性。FC<250 μg/g、CRP<5 mg/L 和 CDAI<150 对随机分组后 48 周时 CDEIS<4 和无深溃疡的敏感性/特异性为 72%/63%,阳性/阴性预测值为 86%/42%。
本 CALM 的事后分析表明,FC<250 μg/g 的截止值是 CD 黏膜愈合的有用替代标志物。