Szymanska Edyta, Dadalski Maciej, Grajkowska Wieslawa, Szymanska Sylwia, Pronicki Maciej, Kierkus Jaroslaw
Department of Paediatrics, Nutrition and Metabolic Disorders, Children's Memorial Health Institute, Warsaw, Poland.
Department of Gastroenterology, Hepatology, and Feeding Disorders, Children's Memorial Health Institute, Warsaw, Poland.
Prz Gastroenterol. 2017;12(1):44-48. doi: 10.5114/pg.2016.64746. Epub 2016 Dec 20.
Deep remission, defined as clinical remission with mucosal healing (MH), with anti-tumor necrosis factor (TNF)-α agents is a new target for therapy in Crohn's disease (CD). Provided that the efficacy of infliximab (IFX) for induction of MH in CD has been demonstrated, there are much less data for adalimumab (ADA), and none concerning MH on histopathological examination.
To assess the impact of biological therapy with ADA on both endoscopic and histopathological MH in paediatric patients with CD.
Twenty-three children (10 boys and 13 girls) aged 13.0 ±9.3 years with moderate to severely active CD diagnosed at the mean age of 5.5 ±0.83 years were included into the study. Seven (30.4%) patients had been previously treated with infliximab and switched to ADA due to intolerance or loss of response. Colonoscopy and gastroscopy with sample collection were performed in all patients before and after induction treatment with ADA. Clinical activity of the disease was assessed using the Paediatric Crohn's Disease Activity Index (PCDAI), and the endoscopic activity was scored using the Simple Endoscopic Score (SES-CD). Histological changes were evaluated by a self-adapted numerical scoring system.
Four (17.4%) patients reached clinical remission (PCDAI ≤ 10). When comparing data at baseline and at a week after ADA treatment, a significant decrease was observed in median PCDAI and in SES-CD score between the initial and control colonoscopies. We reported a decrease in histological scale, which was not statistically significant. A correlation was found between PCDAI and SES-CD score.
Biological therapy with ADA has a positive impact on endoscopic mucosal healing in paediatric patients with CD, which is not associated with histological evidence of suppression of inflammation. Endoscopic MH correlates better than microscopic one with clinical remission.
深度缓解定义为临床缓解伴黏膜愈合(MH),使用抗肿瘤坏死因子(TNF)-α药物治疗是克罗恩病(CD)的新治疗目标。尽管已证实英夫利昔单抗(IFX)诱导CD患者黏膜愈合的疗效,但关于阿达木单抗(ADA)的数据较少,且尚无组织病理学检查中黏膜愈合的相关数据。
评估ADA生物治疗对儿童CD患者内镜及组织病理学黏膜愈合的影响。
纳入23例年龄为13.0±9.3岁的儿童(10例男孩和13例女孩),他们在平均年龄5.5±0.83岁时被诊断为中度至重度活动性CD。7例(30.4%)患者先前接受过英夫利昔单抗治疗,因不耐受或反应丧失而改用ADA。所有患者在接受ADA诱导治疗前后均进行结肠镜检查和胃镜检查并采集样本。使用儿童克罗恩病活动指数(PCDAI)评估疾病的临床活动度,使用简单内镜评分(SES-CD)对内镜活动度进行评分。通过自适应性数字评分系统评估组织学变化。
4例(17.4%)患者达到临床缓解(PCDAI≤10)。比较基线数据和ADA治疗1周后的数据时,初始结肠镜检查和对照结肠镜检查之间的PCDAI中位数和SES-CD评分均显著降低。我们报告组织学评分有所下降,但无统计学意义。发现PCDAI与SES-CD评分之间存在相关性。
ADA生物治疗对儿童CD患者的内镜黏膜愈合有积极影响,这与炎症抑制的组织学证据无关。内镜下黏膜愈合与临床缓解的相关性优于显微镜下的黏膜愈合。