Diamantina Institute, University of Queensland, Brisbane, QLD
Fiona Stanley Hospital, Perth, WA.
Med J Aust. 2018 Jul 16;209(S2):S22-S27. doi: 10.5694/mja18.00175.
The treatment landscape in severe asthma is changing rapidly, with multiple new therapies emerging that promise to transform patient outcomes. In a patient who is not responding to conventional therapy with inhaled corticosteroids and long-acting β2-agonists, it is important to first consider if the diagnosis of asthma is correct and, second, to reflect on whether readily modifiable factors are contributing to poor asthma control. In selected patients it may be appropriate to consider a modified n-of-1 trial of add-on therapies such as long-acting anti-muscarinic agents, leukotriene blockers, theophylline or low dose macrolide antibiotics. A number of monoclonal antibodies are now available that target the molecular pathways that contribute to asthma pathogenesis, and more such agents are likely to emerge in the near future. These biologicals can be transformative in selected patients, markedly reducing the frequency of asthma exacerbations, and allowing many patients to reduce or eliminate their use of long term oral corticosteroids. If the promise of personalised treatment is to be fully realised, it is important that better methods are developed to target these new and expensive treatments to patients most likely to respond. The ultimate goal of inducing remission or cure of asthma is still some distance away.
在严重哮喘的治疗领域正在迅速变化,多种新疗法不断涌现,有望改变患者的预后。对于那些对吸入性皮质类固醇和长效β2-激动剂常规治疗反应不佳的患者,首先要考虑哮喘的诊断是否正确,其次要反思是否存在容易改变的因素导致哮喘控制不佳。在一些特定的患者中,可以考虑采用附加疗法(如长效抗毒蕈碱药物、白三烯拮抗剂、茶碱或低剂量大环内酯类抗生素)的改良 n-of-1 试验。目前有许多针对哮喘发病机制相关分子途径的单克隆抗体可供选择,而且在不久的将来可能会有更多此类药物问世。这些生物制剂在某些患者中具有显著的改善作用,可显著降低哮喘恶化的频率,并使许多患者减少或消除长期口服皮质类固醇的使用。如果要充分实现个体化治疗的承诺,就必须开发出更好的方法,将这些新的、昂贵的治疗方法针对最有可能产生应答的患者。诱导哮喘缓解或治愈的终极目标还有很长的路要走。