联合靶向治疗炎症性肠病的最新证据

Panu Wetwittayakhlang, Peter L Lakatos
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摘要

生物制剂和小分子已经彻底改变了炎症性肠病(IBD)的医学管理,但它们只对一部分患者有效,它们对改变疾病自然史的影响仍然存在争议。近年来,靶向生物制剂与小分子治疗相结合的概念被引入到IBD的治疗中。双靶向治疗(序贯和联合),即两种靶向治疗的结合,可能是患者突破治疗天花板的合理选择。最近的一项随机临床试验(VEGA)首次提供了对照证据,证明两种生物制剂的短期联合使用可能比单独使用任何一种药物对溃疡性结肠炎(UC)患者的疾病控制更好,而不会危及安全性。克罗恩病和UC的多项研究正在进行中。此外,在接受联合治疗并伴有IBD和肠外表现的IBD患者或难治性IBD患者中,真实证据正在积累。值得注意的是,这些患者中的大多数较早暴露于多种生物制剂,并且对组合中的至少一种制剂失去了反应。这篇综述总结了目前关于这种有吸引力的IBD新治疗方案的知识。显然,需要更多的受控数据来评估最佳时机、疗效和减轻安全问题。
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Current Evidence for Combined Targeted Therapy for the Treatment of Inflammatory Bowel Disease
Abstract Biologicals and small molecules have revolutionized the medical management of inflammatory bowel diseases (IBD), yet they are only effective in a proportion of patients, and their impact on changing the natural history of the disease is still debatable. Recently, the concept of combining targeted biologics and small-molecule therapies has been introduced to the treatment of IBD. Dual-targeted therapy (sequential and combined), which is the combination of two targeted therapies, might be a reasonable choice for patients to break through the therapeutic ceiling. A recent randomized clinical trial (VEGA) provided the first controlled evidence that the short-term combination of two biological agents may lead to superior disease control than either of the agents alone in patients with ulcerative colitis (UC) without jeopardizing safety. Multiple studies are underway in both Crohn’s disease and UC. Additionally, real-world evidence is accumulating in IBD patients receiving combination therapies with concomitant IBD and extraintestinal manifestations or in patients with medically refractory IBD. Of note, the majority of these patients were exposed to multiple biological agents earlier and lost response to at least one of the agents in the combination. This review summarizes current knowledge regarding this attractive novel therapeutic option in IBD. Clearly, more controlled data are needed to evaluate optimal timing, efficacy, and mitigation of safety concerns.
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来源期刊
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发文量
296
审稿时长
10 weeks
期刊最新文献
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