Department of Gastroenterology and Clinical Nutrition, The Royal Children's Hospital Melbourne, Parkville, VIC 3052, Australia.
Department of Paediatrics, Khoo Teck Puat-National University Children's Medical Institute, National University Health System, Singapore 119228, Singapore.
World J Gastroenterol. 2023 Mar 14;29(10):1539-1550. doi: 10.3748/wjg.v29.i10.1539.
The advent of biologics and small molecules in inflammatory bowel disease (IBD) has marked a significant turning point in the prognosis of IBD, decreasing the rates of corticosteroid dependence, hospitalizations and improving overall quality of life. The introduction of biosimilars has also increased affordability and enhanced access to these otherwise costly targeted therapies. Biologics do not yet represent a complete panacea: A subset of patients do not respond to first-line anti-tumor necrosis factor (TNF)-alpha agents or may subsequently demonstrate a secondary loss of response. Patients who fail to respond to anti-TNF agents typically have a poorer response rate to second-line biologics. It is uncertain which patient would benefit from a different sequencing of biologics or even a combination of biologic agents. The introduction of newer classes of biologics and small molecules may provide alternative therapeutic targets for patients with refractory disease. This review examines the therapeutic ceiling in current treatment strategies of IBD and the potential paradigm shifts in the future.
生物制剂和小分子药物在炎症性肠病 (IBD) 中的出现标志着 IBD 预后的一个重大转折点,降低了皮质类固醇依赖、住院率,并提高了整体生活质量。生物类似药的引入也提高了这些昂贵的靶向治疗药物的可及性和可负担性。生物制剂还远非一种万能药:一部分患者对一线抗肿瘤坏死因子 (TNF)-α 药物没有反应,或者随后表现出二次应答丧失。对 TNF 药物无应答的患者对二线生物制剂的应答率通常较低。尚不确定哪种患者会从生物制剂的不同排序或甚至联合使用生物制剂中获益。新型生物制剂和小分子药物的出现可能为难治性疾病患者提供了替代的治疗靶点。本文综述了当前 IBD 治疗策略的治疗上限以及未来可能出现的范式转变。