Boulet Louis-Philippe, Chanez Pascal
aQuebec Heart and Lung Institute, Laval University, Québec City, Quebec, Canada bDépartement des Maladies Respiratoires APHM, Laboratoire INSERM CNRS U, 1067, UMR7333, Aix-Marseille University, Marseille, France.
Curr Opin Allergy Clin Immunol. 2015 Jun;15(3):213-9. doi: 10.1097/ACI.0000000000000165.
To determine the benefits of new asthma drugs or therapies, they should be assessed with regard to their effects on relevant clinical outcomes.
The most frequently used outcomes have been symptoms, rescue medication needs and pulmonary function tests, although others such as quality of life, exacerbations and impairment of activities have also been identified as important ones. Improvements in our understanding of basic mechanisms of asthma have led to the development of new sets of outcomes including inflammatory markers and a rapidly increasing number of biomarkers, which however require validation, and assessment of their clinical usefulness. Many studies have not only looked at induced sputum cell differentials or FENO to phenotype asthma but also as treatment efficacy markers. Periostin is considered a marker of TH2-induced airway inflammation and a predictor of response to drugs such as anti-IL13 and omalizumab, although at the individual level, such prediction remains imperfect.
There is a need to develop new markers of activity of the disease, with a prognostic value with regard to the benefits of new treatments.
为确定新型哮喘药物或疗法的益处,应评估它们对相关临床结局的影响。
最常用的结局指标是症状、急救药物需求和肺功能测试,不过生活质量、病情加重和活动受限等其他指标也被视为重要指标。我们对哮喘基本机制认识的提高促使了新的结局指标的产生,包括炎症标志物以及数量迅速增加的生物标志物,然而这些指标需要验证并评估其临床实用性。许多研究不仅将诱导痰细胞分类或呼出气一氧化氮(FENO)用于哮喘表型分析,还将其作为治疗疗效标志物。骨膜蛋白被认为是TH2诱导的气道炎症标志物以及对抗IL-13和奥马珠单抗等药物反应的预测指标,不过在个体层面,这种预测仍不完善。
有必要开发新的疾病活动标志物,这些标志物对新治疗方法的益处具有预后价值。