Faculté de Médecine, Univ. Paris-Sud, Université Paris-Saclay, Le Kremlin-Bicêtre.
Service de Pneumologie, Assistance Publique Hôpitaux de Paris, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.
Curr Opin Pulm Med. 2018 Jan;24(1):83-93. doi: 10.1097/MCP.0000000000000438.
PURPOSE OF REVIEW: Despite currently available treatments, many asthma patients remain inadequately controlled, but identifying distinct patient populations (phenotypes/endotypes) may optimize their management. This review discusses some of the controversies and opportunities for improved disease control in severe asthma. RECENT FINDINGS: Currently approved anti-immunoglobulin E and anti-interleukin 5 biologics, which target specific pathways instead of using a 'one size fits all' strategy, are efficacious and well tolerated therapies for severe asthma. The appropriate use of these biologics, and of those in development (e.g., benralizumab and dupilumab), should be aided by further understanding of asthma phenotypes and endotypes, utilizing appropriate biomarkers.Oral corticosteroids are often added as maintenance therapy for patients with severe uncontrolled asthma, but their use is associated with significant adverse effects and should be considered a last option. The true cost of this therapy, including the cost of morbidities associated with its use, remains to be determined.Severe asthma in pediatrics poses a unique opportunity for possible prevention strategies and the potential for primary prevention. Although several avenues for primary prevention are being explored and are out of the scope of this review, we focus our discussion on the use of omalizumab, which has been recently explored in clinical trials. SUMMARY: Appropriate use of biologics in severe asthma should be supported by further understanding of biomarkers predicting response to targeted therapy. Because of their association with significant adverse effects, add-on oral corticosteroids should be considered a last treatment option for patients with uncontrolled severe asthma. Finally, severe asthma in pediatrics poses a unique opportunity for potential prevention strategies.
目的综述:尽管目前有多种治疗方法,但许多哮喘患者的病情仍控制不佳。确定不同的患者人群(表型/内型)可能会优化他们的管理。本文讨论了一些在重度哮喘中提高疾病控制水平的争议和机会。
最近的发现:目前批准的抗免疫球蛋白 E 和抗白细胞介素 5 生物制剂,针对特定途径而不是采用“一刀切”的策略,是治疗重度哮喘有效且耐受性良好的疗法。这些生物制剂(如 benralizumab 和 dupilumab)以及正在开发的生物制剂的适当使用,应通过进一步了解哮喘表型和内型,并利用适当的生物标志物来辅助。
口服皮质类固醇通常作为重度未控制哮喘患者的维持治疗添加,但它们的使用与显著的不良反应相关,应被视为最后选择。这种治疗的真正成本,包括与使用相关的发病率成本,仍有待确定。儿科重度哮喘为可能的预防策略和潜在的一级预防提供了独特的机会。虽然正在探索几种一级预防途径,且这些途径不在本文综述范围内,但我们将讨论重点放在奥马珠单抗的使用上,它最近已在临床试验中得到探索。
总结:在重度哮喘中,生物制剂的合理使用应通过进一步了解预测靶向治疗反应的生物标志物来支持。由于它们与显著的不良反应相关,添加口服皮质类固醇应被视为未控制的重度哮喘患者的最后治疗选择。最后,儿科重度哮喘为潜在的预防策略提供了独特的机会。
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