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首页> 外文期刊>Annals of allergy, asthma, and immunology >Small molecule drugs for atopic dermatitis, rheumatoid arthritis, and hereditary angioedema
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Small molecule drugs for atopic dermatitis, rheumatoid arthritis, and hereditary angioedema

机译:治疗特应性皮炎、类风湿性关节炎和遗传性血管性水肿的小分子药物

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Objective: To review recent trends in the development of targeted small molecule drugs (SMDs) for the treatment of immunologically driven disorders, including atopic dermatitis, rheumatoid arthritis, and hereditary angioedema. Data sources: Data sources included peer-reviewed published literature from the PubMed database, published abstracts from scientific and medical meetings, and medication information from the Drugs@FDA database. Study selections: Articles with primary or retrospective trial results, articles with patient or physician survey results, articles providing expert perspectives, and commentary on chronic immunologic disorders, Food and Drug Administration package inserts, and abstracts from scientific meetings were selected. Results: Targeted biological therapies have greatly improved response rates and symptom relief for patients with long-term immunologically driven disorders over the past 2 decades. However, recent advances in the understanding of molec-ular pathways involved in the pathogenesis of these disorders have led to the development of novel targeted SMDs, such as tofacitinib and berotralstat, that can be delivered orally or topically. Few head-to-head studies that compare the safety and efficacy of biologics to SMDs in immunologically driven disorders exist, although some studies suggest that oral and topical modes of administration are preferred by patients and may improve patient quality of life over time. Conclusion: Scientific advances have led to an increase in the development of targeted SMDs for the treatment of chronic immunologic disorders, which may revolutionize the management of these diseases. Head-to-head studies and real-world evidence are needed to fully compare treatment attributes between biologics and SMDs, including safety, efficacy, adherence, impact on quality of life, and cost-effectiveness. (c) 2021 American College of Allergy, Asthma Immunology. Published by Elsevier Inc. All rights reserved.
机译:目的:综述靶向小分子药物(SMDs)治疗免疫驱动疾病(包括特应性皮炎、类风湿性关节炎和遗传性血管性水肿)的最新发展趋势。数据来源:数据来源包括来自 PubMed 数据库的同行评审已发表文献、已发表的科学和医学会议摘要以及来自 Drugs@FDA 数据库的药物信息。研究选择:选择具有主要或回顾性试验结果的文章、包含患者或医生调查结果的文章、提供专家观点的文章以及慢性免疫疾病评论、美国食品和药物管理局包装说明书以及科学会议摘要。结果:在过去 2 年中,靶向生物疗法大大提高了长期免疫驱动性疾病患者的反应率和症状缓解。然而,最近对参与这些疾病发病机制的分子通路的理解取得了进展,导致了新型靶向 SMD 的开发,例如托法替尼和贝罗司他,它们可以口服或局部给药。很少有头对头研究将生物制剂与 SMD 在免疫驱动疾病中的安全性和有效性进行比较,尽管一些研究表明口服和局部给药方式是患者的首选,并且随着时间的推移可能会改善患者的生活质量。结论:随着科学的进步,用于治疗慢性免疫疾病的靶向SMDs的开发有所增加,这可能会彻底改变这些疾病的管理。需要头对头研究和真实世界证据来充分比较生物制剂和SMD之间的治疗属性,包括安全性、有效性、依从性、对生活质量的影响和成本效益。(c) 2021 年美国过敏、哮喘和免疫学会。由以下开发商制作:Elsevier Inc.保留所有权利。

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