Long-term safety, durability of response, cessation and switching of biologics.

IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM
Current Opinion in Pulmonary Medicine Pub Date : 2024-05-01 Epub Date: 2024-03-01 DOI:10.1097/MCP.0000000000001067
Arjun Mohan, Anna Y Qiu, Njira Lugogo
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引用次数: 0

Abstract

Purpose of review: Severe asthma patients suffer from decreased quality of life, and increased asthma symptoms, exacerbations, hospitalizations, and risk of death. Biologics have revolutionized treatment for severe asthma. However, with multiple biologic agents now available, clinicians must consider initial selection the long-term effectiveness of biologics. Additionally, patients have overlapping eligibilities and clinicians may consider switching between biologics for improved response. Finally, careful assessment of biologics cessation is needed for severe asthma patients who depend on these add-on therapies for asthma control.

Recent findings: Evidence for long-term durability and safety varies by biologic agent. In general, initial benefits noted from these agents (ex. exacerbation reduction) is, at minimum, sustained with long term use. Rates of adverse events and serious adverse events, including those requiring cessation of a biologics are low with long term use. Further studies are needed to understand the development of antidrug antibodies but currently their prevalence rates are low. Adverse events and insufficient efficacy are common reasons for biologic cessation or switching. Discontinuation maybe associated with waning of benefits but can be considered in certain situations. Biologic switching can be associated with improved asthma control.

Summary: Biologics are safe and effective long-term therapies for the management of asthma. Discontinuation must be carefully considered and if possible avoided. Reasons for insufficient efficacy must be evaluated and if needed, biologic switching should be considered.

长期安全性、反应的持久性、生物制剂的停用和转换。
审查目的:重症哮喘患者的生活质量下降,哮喘症状、病情加重、住院治疗和死亡风险增加。生物制剂彻底改变了重症哮喘的治疗方法。然而,由于现在有多种生物制剂可供选择,临床医生必须考虑生物制剂的初始选择和长期疗效。此外,患者的治疗资格存在重叠,临床医生可考虑在不同生物制剂之间进行转换,以改善治疗效果。最后,对于依赖这些附加疗法来控制哮喘的重症哮喘患者,需要仔细评估生物制剂的停用情况:生物制剂的长期持久性和安全性证据各不相同。一般来说,这些药物的初期疗效(如减少病情恶化)至少在长期使用后可以持续。长期使用生物制剂的不良反应和严重不良反应(包括需要停药的不良反应)发生率较低。需要进一步研究了解抗药性抗体的发展情况,但目前其发生率较低。不良反应和疗效不佳是停用或更换生物制剂的常见原因。停药可能会导致疗效减弱,但在某些情况下可以考虑停药。总结:生物制剂是治疗哮喘安全有效的长期疗法。必须慎重考虑并尽可能避免停药。必须评估疗效不佳的原因,如有必要,应考虑更换生物制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
109
审稿时长
6-12 weeks
期刊介绍: ​​​​​​Current Opinion in Pulmonary Medicine is a highly regarded journal offering insightful editorials and on-the-mark invited reviews, covering key subjects such as asthma; cystic fibrosis; infectious diseases; diseases of the pleura; and sleep and respiratory neurobiology. Published bimonthly, each issue of Current Opinion in Pulmonary Medicine introduces world renowned guest editors and internationally recognized academics within the pulmonary field, delivering a widespread selection of expert assessments on the latest developments from the most recent literature.
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