Division of Pediatric Gastroenterology, Federal University of São Paulo, São Paulo, Brazil.
J Pediatr Gastroenterol Nutr. 2010 Jun;50(6):628-33. doi: 10.1097/MPG.0b013e3181bbf481.
The objective of the study was to evaluate the response to infliximab in children and adolescents with Crohn disease and ulcerative colitis up to week 22.
A total of 21 patients with inflammatory bowel disease (IBD) received 5 mg/kg of infliximab at weeks 0, 2, 6, and 14. The following parameters were evaluated: clinical manifestations; activity indices of IBD, including the Pediatric Crohn Disease Activity Index for Crohn disease, the Lightiger Colitis Activity Index and the Pediatric Ulcerative Colitis Activity Index for ulcerative colitis, and the modified Harvey-Bradshaw Index for Crohn disease and ulcerative colitis; and the reduction or suspension of corticosteroid use.
All of the patients had improvements in clinical manifestations after the first infusion of infliximab. At week 22, 18 of 21 (85.7%) patients were categorized as being in remission, 3 of 21 (14.3%) patients were categorized as having clinical improvement, and none of the patients were categorized as having no response. There was a statistically significant difference in all of the IBD activity indices at weeks 2, 6, 14, and 22 compared with time 0. The corticosteroid use was completely discontinued in 6 of 15 patients by week 22.
Infliximab is effective in the treatment of Crohn disease and ulcerative colitis in children and adolescents up to week 22.
本研究旨在评估英夫利昔单抗在儿童和青少年克罗恩病和溃疡性结肠炎患者中的应答情况,随访时间至 22 周。
共 21 例炎症性肠病(IBD)患者在第 0、2、6 和 14 周接受 5mg/kg 的英夫利昔单抗治疗。评估以下参数:临床表现;IBD 活动指数,包括克罗恩病的儿科克罗恩病活动指数、溃疡性结肠炎的轻型结肠炎活动指数和儿童溃疡性结肠炎活动指数,以及克罗恩病和溃疡性结肠炎的改良 Harvey-Bradshaw 指数;以及皮质类固醇的使用减少或暂停。
所有患者在首次输注英夫利昔单抗后临床症状均有改善。在第 22 周,21 例患者中有 18 例(85.7%)缓解,21 例中有 3 例(14.3%)临床改善,无一例无应答。与基线相比,在第 2、6、14 和 22 周时,所有 IBD 活动指数均有统计学差异。在第 22 周时,15 例患者中有 6 例完全停用皮质类固醇。
英夫利昔单抗治疗儿童和青少年克罗恩病和溃疡性结肠炎有效,随访时间至 22 周。