类风湿性关节炎和银屑病关节炎的双重生物治疗。

IF 1.4 Q2 MEDICINE, GENERAL & INTERNAL Rambam Maimonides Medical Journal Pub Date : 2023-04-30 DOI:10.5041/RMMJ.10494
Victoria Furer, Ori Elkayam
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引用次数: 2

摘要

生物制剂治疗已成为治疗免疫介导性疾病(IMD)的标准治疗方法,包括类风湿关节炎和银屑病关节炎。然而,相当比例的患者经历对生物制剂的反应丧失,需要增加治疗,或产生副作用。在过去的十年中,具有不同靶向分子途径的新生物制剂已被批准用于治疗IMD,从而引入了双重生物治疗的可能性。针对不同炎症途径的双重生物治疗的作用已成为IMD领域的一个非常感兴趣的领域,解决难治性疾病患者未满足的临床需求和治疗合并症,如骨质疏松症、哮喘、特应性皮炎和荨麻疹。尽管越来越多地使用生物制剂作为不同适应症的双重治疗,但有关同时使用一种以上生物制剂的安全性的数据缺乏。本综述的目的是总结目前在类风湿性关节炎和银屑病关节炎患者中使用双生物制剂的文献,解决联合治疗相关的潜在不良反应,并强调未来使用这种新型治疗方式的方向。
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Dual Biologic Therapy in Patients with Rheumatoid Arthritis and Psoriatic Arthritis.

Treatment with biological agents has become standard of care in treatment of immune-mediated diseases (IMD), including rheumatoid arthritis and psoriatic arthritis. Yet, a significant proportion of patients experience loss of response to biologics, need treatment escalation, or develop side effects. During the past decade, new biologic agents with different targeted molecular pathways have been approved for treatment of IMD, introducing the possibility of concomitant dual biologic therapy. The role of dual biologic therapy targeting different inflammatory pathways has become an area of great interest in the field of IMD, addressing the unmet clinical need of patients with refractory diseases and treatment of comorbidities, such as osteoporosis, asthma, atopic dermatitis, and urticaria. Despite the increasing use of biologics as a dual therapy across different indications, there is a paucity of data concerning the safety of the simultaneous use of more than one biological agents. The purpose of this review is to summarize the current literature on the use of dual biologics in patients with rheumatoid arthritis and psoriatic arthritis, addressing the potential adverse effects associated with combination therapy, and highlighting future directions in the use of this novel therapeutic modality.

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来源期刊
Rambam Maimonides Medical Journal
Rambam Maimonides Medical Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
3.20
自引率
6.70%
发文量
55
审稿时长
8 weeks
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