用单克隆抗体联合治疗重症哮喘和免疫介导的炎症性疾病:综述。

IF 1.1 Q4 RESPIRATORY SYSTEM
Lorenzo Carriera, Sara Caporuscio, Marta Fantò, Alice D'Abramo, Genesio Puzio, Luca Triolo, Angelo Coppola
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引用次数: 0

摘要

生物药物彻底改变了严重哮喘的治疗方法,量体裁衣的治疗方法使缓解成为可以实现的治疗目标。在世界许多地方,自身免疫性疾病的发病率正在上升。重症哮喘患者在符合条件或已接受哮喘批准生物制剂治疗的情况下,可能还患有另一种免疫介导的炎症性疾病(IMID),需要同时使用第二种单克隆抗体。通过对单克隆抗体在线数据库进行系统检索,我们收集并分析了文献中关于同时使用一种哮喘批准生物制剂和另一种生物制剂治疗另一种免疫性疾病的真实研究。根据预先规定的纳入和排除标准,本综述共纳入了 26 篇文章。所有纳入的论文均为回顾性研究。研究设计包括病例报告(18 篇)、系列病例(3 篇)、回顾性图表回顾(3 篇)、回顾性观察研究(1 篇)和队列研究(1 篇)。本研究旨在介绍目前文献中所有已获批准的重症哮喘生物制剂与单克隆抗体针对不同适应症的给药组合。根据第二种具有不同作用机制的生物制剂的处方对象 IMID 进行分组。讨论部分对专门治疗不受控制的重症哮喘患者的组合处方进行了更深入的评估,因为对这些来自实际生活经验的治疗组合进行分析可能有助于优化重症哮喘患者的管理,最终改善患者护理和治疗效果。需要进行前瞻性登记和未来研究,以评估 IMID 重症哮喘患者接受联合疗法的安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combination treatment with monoclonal antibodies for the management of severe asthma and immune-mediated inflammatory diseases: a comprehensive review.

Biological drugs have revolutionized the management of severe asthma, and a tailored treatment approach made it possible to consider remission as an achievable treatment target. The incidence of autoimmune diseases is increasing in many parts of the world. Patients suffering from severe asthma, eligible or already treated with an asthma-approved biologic agent, may suffer from another immune-mediated inflammatory disease (IMID) that could require the simultaneous use of a second monoclonal antibody. The real-life studies available in the literature describing the concurrent administration of an asthma-approved biologic agent with another biologic for a different immune disease, obtained through a systematic search on online databases based on monoclonal antibodies, were collected and analyzed. 26 articles were included in this review according to the prespecified inclusion and exclusion criteria. All included papers were retrospective in nature. Study designs were case reports (n=18), case series (n=3), retrospective chart reviews (n=3), retrospective observational studies (n=1), and cohort studies (n=1). The study is intended to present, within the current literature, all the administered combinations of severe asthma-approved biologics with monoclonal antibodies for a different indication. Those were grouped according to the IMID for whom the second biologic agent, with a different mechanism of action, was prescribed. The combinations prescribed to the cohort of patients specifically treating uncontrolled severe asthma were deeper evaluated in the discussion section, since an analysis of these therapeutic combinations deriving from real-life experiences may be useful to optimize the management of patients with severe asthma, ultimately leading to improved patient care and outcomes. Prospective registries and future studies are required to assess the safety and efficacy of combination therapies for severe asthmatic patients who suffer from an IMID.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
1
审稿时长
12 weeks
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