University of South Florida, Tampa, Fla.
HealthyAirways, Madison, Wis.
J Allergy Clin Immunol Pract. 2019 Jan;7(1):156-164.e1. doi: 10.1016/j.jaip.2018.04.043. Epub 2018 May 22.
Omalizumab has demonstrated efficacy in clinical trials of patients with asthma, but real-world data are needed.
To assess outcomes after omalizumab initiation in patients with asthma in a real-world setting.
Patients aged 12 years and older with allergic asthma who were candidates for omalizumab on the basis of physician-assessed need were enrolled in a US-based, prospective, single-arm, 48-week multicenter study, the Prospective Observational Study to Evaluate Predictors of Clinical Effectiveness in Response to Omalizumab. Monthly assessments included exacerbations, health care utilization, asthma control test (ACT), and adverse events. At baseline, 6 months, and end of study, biomarkers (blood eosinophils and fractional exhaled nitric oxide) were collected and spirometry performed.
Of 806 enrollees, 801 (99.4%) received omalizumab and 622 (77.2%) completed the study. The exacerbation rate significantly improved from a mean of 3.00 ± 3.28 in the 12 months before baseline to 0.78 ± 1.37 through month 12 (P < .001) and was similar in adults and adolescents; there was a reduction of 81.9% in the percentage of patients with 1 or more hospitalizations. Lung function remained generally unchanged. A mean improvement of 4.4 ± 4.9 in ACT scores was observed. Eighty-seven percent of patients were responders on the basis of clinical improvement in exacerbations, lung function, or ACT scores. Baseline biomarker status was associated with ACT scores and lung function improvement, but the magnitude of this improvement was not clinically relevant. No new safety signals emerged.
Omalizumab initiation in patients with asthma resulted in improved exacerbation rates, reduced hospitalizations, and improved ACT scores compared with pretreatment values, regardless of biomarker status.
奥马珠单抗在哮喘患者的临床试验中已显示出疗效,但仍需要真实世界的数据。
评估奥马珠单抗在真实环境中起始治疗哮喘患者的结局。
在一项基于美国的、前瞻性的、单臂、48 周多中心研究中,纳入了年龄在 12 岁及以上、基于医生评估需求适合奥马珠单抗治疗的过敏性哮喘患者。该研究名为奥马珠单抗有效性预测因素的前瞻性观察性研究。每月评估包括哮喘加重、医疗保健利用、哮喘控制测试(ACT)和不良事件。在基线、6 个月和研究结束时,收集生物标志物(血嗜酸性粒细胞和呼出气一氧化氮分数)并进行肺量测定。
在 806 名入组患者中,801 名(99.4%)接受了奥马珠单抗治疗,622 名(77.2%)完成了研究。与基线前 12 个月的平均 3.00±3.28 相比,哮喘加重率在第 12 个月时显著改善至 0.78±1.37(P<.001),且在成年患者和青少年患者中相似;住院患者比例减少了 81.9%。肺功能基本保持不变。ACT 评分平均提高了 4.4±4.9。根据哮喘加重、肺功能或 ACT 评分的临床改善,87%的患者为应答者。基线生物标志物状态与 ACT 评分和肺功能改善相关,但改善幅度无临床意义。未出现新的安全性信号。
与治疗前相比,奥马珠单抗起始治疗哮喘患者可改善哮喘加重率、减少住院次数并提高 ACT 评分,无论生物标志物状态如何。