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基于 SONIC 数据的事后分析验证克罗恩病患者内镜活动评分的有效性。

Validation of endoscopic activity scores in patients with Crohn's disease based on a post hoc analysis of data from SONIC.

机构信息

Department of Gastroenterology, University Hospitals Leuven, Leuven, Belgium.

出版信息

Gastroenterology. 2013 Nov;145(5):978-986.e5. doi: 10.1053/j.gastro.2013.08.010. Epub 2013 Aug 14.

Abstract

BACKGROUND & AIMS: Mucosal healing might alter midterm and long-term outcomes of patients with Crohn's disease (CD) and has become an important end point in clinical trials. However, the minimal degree of mucosal improvement (endoscopic response) required to alter midterm outcomes is not known. We aimed to determine the best definition of endoscopic response by evaluating data on the Simple Endoscopic Score for Crohn's Disease (SES-CD) and the Crohn's Disease Endoscopic Index of Severity (CDEIS) from the Study of Biologic and Immunomodulator Naive Patients in Crohn's Disease (SONIC trial).

METHODS

We analyzed data from 172 patients who participated in the SONIC trial, were found to have endoscopic lesions at baseline, and underwent a second endoscopic examination at week 26 of treatment with infliximab, azathioprine, or both. Mucosal healing was defined as absence of ulcers. A central reader calculated SES-CD and CDEIS results. Different cutoff values were set for endoscopic response based on the SES-CD or CDEIS. The diagnostic ability of these different cutoff values was evaluated using receiver operating characteristic (ROC) curves, positive likelihood ratios (PLR), and negative likelihood ratios (NLR). Corticosteroid-free clinical remission (CFREM) at week 50 was used as a binary classifier.

RESULTS

Based on analyses of ROC curves, PLR, and NLR, endoscopic response was defined as a decrease from baseline in SES-CD of at least 50%. At week 26, mucosal healing and endoscopic response were achieved in 48% and 65% of patients, respectively. Mucosal healing at week 26 was associated with CFREM at week 50, with 56% sensitivity, 65% specificity, a PLR of 1.60, and an NLR of 0.67. Endoscopic response at week 26 was associated with CFREM at week 50, with 74% sensitivity, 48% specificity, a PLR of 1.42, and an NLR of 0.54. Endoscopic response, defined as a decrease from baseline in CDEIS of at least 50%, yielded similar results.

CONCLUSIONS

In patients with CD, mucosal healing and endoscopic response (defined as a decrease from baseline in SES-CD or CDEIS of at least 50%) at week 26 of treatment identified those most likely to be in CFREM at week 50. The ability of the proposed endoscopic response cutoff value to predict midterm CFREM should be validated in an independent, prospective cohort. Its correlation with changes in long-term disease progression still needs to be demonstration. ClinicalTrials.gov, Number: NCT00094458.

摘要

背景与目的

黏膜愈合可能改变克罗恩病(CD)患者的中期和长期结局,并且已成为临床试验中的一个重要终点。然而,目前尚不清楚黏膜改善(内镜应答)的最低程度,这种改善需要改变中期结局。我们旨在通过评估 SONIC 试验中生物制剂和免疫调节剂初治克罗恩病患者的简单克罗恩病内镜评分(SES-CD)和克罗恩病内镜严重指数(CDEIS)的数据,来确定内镜应答的最佳定义。

方法

我们分析了 172 名参与 SONIC 试验的患者的数据,这些患者在基线时存在内镜病变,并在接受英夫利昔单抗、硫唑嘌呤或两者治疗 26 周后接受了第二次内镜检查。黏膜愈合定义为无溃疡。一位中央读者计算了 SES-CD 和 CDEIS 的结果。根据 SES-CD 或 CDEIS 设置不同的内镜应答截断值。使用受试者工作特征(ROC)曲线、阳性似然比(PLR)和阴性似然比(NLR)评估这些不同截断值的诊断能力。第 50 周无皮质类固醇的临床缓解(CFREM)被用作二分类器。

结果

基于 ROC 曲线、PLR 和 NLR 的分析,内镜应答被定义为 SES-CD 自基线下降至少 50%。在第 26 周,分别有 48%和 65%的患者实现了黏膜愈合和内镜应答。第 26 周的黏膜愈合与第 50 周的 CFREM 相关,其灵敏度为 56%,特异性为 65%,PLR 为 1.60,NLR 为 0.67。第 26 周的内镜应答与第 50 周的 CFREM 相关,其灵敏度为 74%,特异性为 48%,PLR 为 1.42,NLR 为 0.54。以 SES-CD 或 CDEIS 自基线下降至少 50%定义的内镜应答也得到了类似的结果。

结论

在 CD 患者中,第 26 周治疗时的黏膜愈合和内镜应答(定义为 SES-CD 或 CDEIS 自基线下降至少 50%)可识别出第 50 周最有可能达到 CFREM 的患者。该建议的内镜应答截断值预测中期 CFREM 的能力应在独立的前瞻性队列中得到验证。其与长期疾病进展变化的相关性仍需证明。ClinicalTrials.gov,注册号:NCT00094458。

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