Institute for Maternal and Child Health IRCCS "Burlo Garofolo", Trieste, Italy.
Department of Pathology, Spedali Civili, Brescia, Italy.
Clin Gastroenterol Hepatol. 2017 Sep;15(9):1382-1389.e1. doi: 10.1016/j.cgh.2017.02.029. Epub 2017 Mar 7.
BACKGROUND & AIMS: Mucosal healing, determined by endoscopic evaluation, is one of the most important prognostic markers for patients with inflammatory bowel diseases. Findings from histologic evaluation, however, could complement findings from endoscopy in assessing mucosal responses to treatment. We analyzed long-term results of children treated with thalidomide to determine the association between clinical response and histology and endoscopy findings.
We collected data from 2 multicenter trials of 70 children with refractory Crohn's disease (CD) or ulcerative colitis (UC) (2-18 years old; ileocolonic or colonic disease) given thalidomide or placebo (NCT00720538). Clinical remission and clinical response at 8 weeks were defined as a pediatric CD activity index scores 10 points or lower and a decrease of at least 50% from baseline, respectively, for patients with CD; and as a pediatric UC activity index score below 10 and a decrease of at least 20 points from baseline, respectively, for patients with UC. Patients with a clinical response to 8 weeks' treatment with thalidomide underwent endoscopic examination with biopsy collection at study weeks 12 and 52. Severity of inflammation in patients with UC was assessed by Mayo score and in patients with CD by 4-grade system. Biopsies were assessed for signs of active inflammation, erosion or ulceration, and crypt abscesses and assigned a histologic score.
Clinical remission was observed in 42 patients (60.0%) and clinical response in 45 patients (64.2%) at Week 8. At Week 52, a total of 38 patients (54.3%) were still in clinical remission or still had a clinical response; 29 patients (41.4%) had mucosal healing, defined as complete healing of erosions or ulcerations, and 20 patients (27.7%) had histologic healing, defined as complete absence of markers of inflammation. Of patients with clinical remission or clinical response, 75.3% also had mucosal healing and 52.6% also had histologic healing. The probability of achieving mucosal healing decreased significantly with increasing values of erythrocyte sedimentation rate (adjusted odds ratio, 0.96; 95% CI, 0.93-0.98; P = .006).
In a long-term analysis of data from 2 clinical trials of pediatric patients with CD or UC, 52 weeks' treatment with thalidomide led to clinical remission in 54.3% of patients with ileocolonic or colonic disease; of these patients, 75.3% had mucosal healing and 52.6% also had histologic healing. Further studies are needed to determine how thalidomide therapy affects long-term progression of inflammatory bowel diseases. (ClinicalTrials.gov number NCT00720538).
内镜评估的黏膜愈合是炎症性肠病(IBD)患者最重要的预后标志物之一。然而,组织学评估的结果可以补充内镜评估,从而评估治疗对黏膜的反应。我们分析了接受沙利度胺治疗的儿童的长期结果,以确定临床缓解与组织学和内镜检查结果之间的关联。
我们从 2 项多中心试验中收集了 70 例患有难治性克罗恩病(CD)或溃疡性结肠炎(UC)的儿童(2-18 岁;回肠结肠或结肠疾病)的数据,这些儿童接受了沙利度胺或安慰剂治疗(NCT00720538)。临床缓解和 8 周时的临床反应定义为 CD 患者的儿科 CD 活动指数评分降低 10 分或更低,与基线相比降低至少 50%;UC 患者的儿科 UC 活动指数评分低于 10 分,与基线相比降低至少 20 分。对 8 周沙利度胺治疗有临床反应的患者在第 12 周和第 52 周接受内镜检查和活检。UC 患者的炎症严重程度采用 Mayo 评分评估,CD 患者采用 4 级系统评估。对活检标本进行活跃炎症、糜烂或溃疡以及隐窝脓肿的评估,并给出组织学评分。
在第 8 周时,42 例(60.0%)患者达到临床缓解,45 例(64.2%)患者达到临床反应。在第 52 周时,共有 38 例(54.3%)患者仍处于临床缓解或仍有临床反应;29 例(41.4%)患者达到黏膜愈合,定义为糜烂或溃疡完全愈合,20 例(27.7%)患者达到组织学愈合,定义为炎症标志物完全消失。在有临床缓解或临床反应的患者中,75.3%的患者也有黏膜愈合,52.6%的患者也有组织学愈合。随着红细胞沉降率(ESR)值的增加,达到黏膜愈合的概率显著降低(调整优势比,0.96;95%CI,0.93-0.98;P=0.006)。
在对 2 项儿科 CD 或 UC 患者临床试验数据的长期分析中,52 周的沙利度胺治疗导致 54.3%的回肠结肠或结肠疾病患者达到临床缓解;在这些患者中,75.3%达到黏膜愈合,52.6%达到组织学愈合。需要进一步研究沙利度胺治疗如何影响 IBD 的长期进展。(临床试验.gov 编号 NCT00720538)。