聚焦生物制剂:阿拉伯联合酋长国(UAE)当前克罗恩病生物和小分子疗法的全面回顾

Laith Alrubaiy, L. Pitsillides, Thomas O’Connor, Matilda Woodhill, Harry Higgins, T. K. Swaid, Doa’a Alkhader, Z. Koutoubi
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引用次数: 0

摘要

导言:与世界其他地区一样,中东地区的克罗恩病(CD)治疗也随着新型先进医疗和生物疗法的引入而迅速发展。在阿拉伯联合酋长国(UAE),一些生物疗法被用于缓解严重和耐药的克罗恩病病例。我们进行了文献检索,以分析目前在阿联酋获得许可的生物疗法的有效性和安全性。方法:我们检索了 PubMed、Embase 和 Cochrane 图书馆数据库中从开始到 2020 年 1 月的相关研究。检索词是根据 CD 的既定治疗指南生成的。我们还人工检索了相关文献的书目,以获取更多论文。结果:治疗CD的生物制剂和小分子药物包括四类核心药物:抗肿瘤坏死因子-α制剂(TNF-α)、整合素受体拮抗剂、Janus激酶(JAK)抑制剂和IL-12/IL-23拮抗剂。所有类别的药物在治疗 CD 患者方面均显示出良好的疗效和安全性。某些类别的药物具有不同的副作用。其中包括 TNF-α 和整合素受体拮抗剂会增加淋巴瘤和结核病的风险。许多试验支持这些已获许可药物的有效性。生物制剂不耐受很常见;三分之一接受TNF-α治疗的患者会对该特定药物产生不耐受。结论在阿联酋获得许可的先进医疗疗法已被证明是安全和有效的。还需要开展更多研究,以评估新型生物制剂和生物仿制药的安全性和疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biologics in Focus: A Comprehensive Review of Current Biological and Small Molecules Therapies for Crohn’s Disease in the United Arab Emirates (UAE)
Introduction: The management of Crohn’s disease (CD) in the Middle East, like in other parts of the world, is rapidly evolving with the introduction of novel advanced medical and biological therapies. In the United Arab Emirates (UAE), several biological therapies are used to achieve remission in severe and resistant cases of CD. We carried out a literature search to analyze the effectiveness and safety of biologic treatments currently licensed in the UAE. Methods: We searched the PubMed, Embase and Cochrane library databases from inception to January 2020 to identify relevant studies. Search terms were generated using established treatment guidelines for CD. We also manually searched the bibliographies of relevant literature to obtain additional papers. Results: Biologic and small molecule agents for CD include four core drug classes: anti-tumor necrosis factor-α agents (TNF-α), integrin receptor antagonists, Janus kinase (JAK) inhibitors and IL-12/IL-23 antagonists. All drug classes showed good efficacy and safety in managing patients with CD. Some drug classes had distinguishable side effect profiles. This included an increased lymphoma and tuberculous risk for TNF-α and integrin receptor antagonists. Many trials supported the effectiveness of these licensed drugs. Biologic agent intolerance was common; one-third of patients receiving TNF-α treatment will develop intolerance to that specific drug. Conclusions: Advanced medical therapies licensed in the UAE have proven to be safe and efficacious. Additional research is required to evaluate the safety and efficacy of newer biologics and biosimilars.
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