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儿童生物制剂与重度哮喘

Biologics and severe asthma in children.

作者信息

Saxena Shikha, Rosas-Salazar Christian, Fitzpatrick Anne, Bacharier Leonard B

机构信息

Division of Pediatric Allergy, Immunology, and Pulmonary Medicine, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee.

Division of Pulmonology, Allergy/Immunology, Cystic Fibrosis and Sleep, Department of Pediatrics, Emory University School of Medicine.

出版信息

Curr Opin Allergy Clin Immunol. 2023 Apr 1;23(2):111-118. doi: 10.1097/ACI.0000000000000880. Epub 2022 Nov 24.

Abstract

PURPOSE OF REVIEW

Severe asthma can carry significant morbidity and mortality for patients, and it places a burden on families and the healthcare system. Biologic agents have revolutionized the care of patients with severe asthma in recent years. Evidence surrounding some of these therapies is limited in the pediatric population, but recent studies show that they significantly improve asthma care when used appropriately. In this review, we discuss the biologic therapies currently approved to treat severe asthma in school-age children and adolescents.

RECENT FINDINGS

Randomized controlled trials have been published in support of biologics in children and/or adolescents. These therapies have been shown to reduce the annual rate of severe asthma exacerbations by at least 40-50%, and some up to about 70%. Improvements in asthma control, lung function, oral corticosteroid use, and quality of life have also been demonstrated, although these vary by agent. Furthermore, these therapies have reassuring safety profiles in pediatric patients.

SUMMARY

With three biologic agents approved for children ages 6-11 years and five approved for adolescents ages >12 years, it can be challenging to select one. The therapy should be chosen after careful consideration of the patient's asthma phenotype and biomarkers. Additional pediatric-specific clinical trials would be helpful in developing evidence-based guidelines on biologic therapies in this population.

摘要

综述目的

重度哮喘会给患者带来严重的发病率和死亡率,给家庭和医疗系统带来负担。近年来,生物制剂彻底改变了重度哮喘患者的治疗方式。在儿科人群中,关于其中一些疗法的证据有限,但最近的研究表明,在适当使用时,它们能显著改善哮喘治疗。在本综述中,我们讨论目前已获批用于治疗学龄儿童和青少年重度哮喘的生物疗法。

最新发现

已发表随机对照试验以支持在儿童和/或青少年中使用生物制剂。这些疗法已被证明可将重度哮喘发作的年发生率降低至少40%-50%,有些可达约70%。哮喘控制、肺功能、口服糖皮质激素使用及生活质量也有改善,尽管因药物而异。此外,这些疗法在儿科患者中的安全性令人放心。

总结

有三种生物制剂获批用于6-11岁儿童,五种获批用于12岁以上青少年,选择其一可能具有挑战性。应在仔细考虑患者的哮喘表型和生物标志物后选择治疗方法。更多针对儿科的临床试验将有助于制定该人群生物疗法的循证指南。

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