From the Massachusetts General Hospital for Children, Harvard Medical School, Boston, MA.
Cincinnati Children's Hospital, Cincinnati, OH.
J Pediatr Gastroenterol Nutr. 2023 May 1;76(5):566-575. doi: 10.1097/MPG.0000000000003734. Epub 2023 Feb 19.
BACKGROUND: Biologic medications are recommended for treatment of moderately-to-severely active Crohn disease (CD) or ulcerative colitis (UC) in children. However, many patients require sequential biologic treatment because of nonresponse or loss of response to the initial biologic. METHODS: We analyzed pediatric inflammatory bowel disease (IBD) data from the ImproveCareNow Network registry between May 2006 and September 2016, including time to biologic initiation, choice of first subsequent biologics, biologic durability, and reasons for discontinuation. RESULTS: Of 17,649 patients with IBD [CD: 12,410 (70%); UC: 5239 (30%)], 7585 (43%) were treated with a biologic agent before age 18 (CD: 50%; UC: 25%). Biologic treatment was more likely for CD than UC (odds ratio, 3.0; 95% CI: 2.8-3.2; P < 0.0001). First biologic agents for all patients were anti-tumor necrosis factor agents (88% infliximab, 12% adalimumab). Probability of remaining on the first biologic was significantly higher in CD than UC ( P < 0.0001). First biologics were discontinued because of loss of response (39%), intolerance (23%), and nonresponse (19%). In univariate analysis, factors associated with discontinuation of first and/or second biologics in CD include colonic-only disease, corticosteroid use, upper gastrointestinal tract involvement, and clinical and biochemical markers of severe disease. Biologic durability improved with later induction date. CONCLUSIONS: Treatment with biologic medications is common in pediatric IBD. Patients with CD are more likely to receive biologics, receive biologics earlier in disease course, and remain on the first biologic longer than patients with UC. Multiple factors may predict biologic durability in children with IBD.
背景:生物制剂被推荐用于治疗中重度活动期克罗恩病(CD)或溃疡性结肠炎(UC)患儿。然而,许多患者需要序贯生物治疗,因为他们对初始生物制剂无应答或应答丧失。
方法:我们分析了 2006 年 5 月至 2016 年 9 月期间 ImproveCareNow 网络注册中心的儿科炎症性肠病(IBD)数据,包括生物制剂起始时间、首次后续生物制剂选择、生物制剂耐久性以及停药原因。
结果:在 17649 例 IBD 患者中[CD:12410(70%);UC:5239(30%)],7585 例(43%)在 18 岁之前接受过生物制剂治疗(CD:50%;UC:25%)。CD 患者比 UC 患者更有可能接受生物制剂治疗(比值比,3.0;95%CI:2.8-3.2;P<0.0001)。所有患者的首种生物制剂均为抗肿瘤坏死因子制剂(88%英夫利昔单抗,12%阿达木单抗)。CD 患者继续使用首种生物制剂的可能性明显高于 UC 患者(P<0.0001)。首种生物制剂因失应答(39%)、不耐受(23%)和无应答(19%)而停用。单因素分析显示,CD 患者停用首种和/或第二种生物制剂的相关因素包括仅结肠受累、皮质类固醇使用、上消化道受累以及严重疾病的临床和生化标志物。生物制剂耐久性随诱导日期的延迟而改善。
结论:生物药物治疗在儿科 IBD 中很常见。CD 患者更有可能接受生物制剂治疗,在疾病过程中更早接受生物制剂治疗,并且继续使用首种生物制剂的时间长于 UC 患者。多种因素可能预测 IBD 儿童的生物制剂耐久性。
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