Skåne University Hospital, Lund University, Lund, Sweden.
Sacré-Coeur Hospital, Université de Montréal, Montreal, QC, Canada.
Chest. 2016 Oct;150(4):789-798. doi: 10.1016/j.chest.2016.03.032. Epub 2016 Apr 4.
This phase 3 study further characterizes the efficacy and safety of reslizumab (a humanized anti-IL-5 monoclonal antibody) in patients aged 12 to 75 years with asthma inadequately controlled by at least a medium-dose inhaled corticosteroid and with a blood eosinophil count ≥ 400 cells/μL.
Patients were randomized to receive reslizumab 0.3 or 3.0 mg/kg or placebo administered once every 4 weeks for 16 weeks (total four doses). The primary end point was change from baseline in pre-bronchodilator FEV over 16 weeks. Secondary end points included FVC, forced expiratory flow at 25% to 75% of FVC (FEF), patient-reported control of asthma symptoms, short-acting β-agonist (SABA) use, blood eosinophil levels, and safety.
Reslizumab significantly improved FEV (difference vs placebo [reslizumab 0.3 and 3.0 mg/kg], 115 mL [95% CI, 16-215; P = .0237] and 160 mL [95% CI, 60-259; P = .0018]). Clinically meaningful increases in FVC (130 mL) and FEF (233 mL/s) were observed with reslizumab 3.0 mg/kg. Reslizumab improved scores on the Asthma Control Questionnaire (ACQ) and Asthma Quality of Life Questionnaire (AQLQ) vs placebo (greater effects seen with 3.0 mg/kg; P < .05). The minimally important difference was reached for the AQLQ (reslizumab 3.0 mg/kg) but not on the ACQ. Scores on the Asthma Symptom Utility Index and SABA use were improved with reslizumab. The most common adverse events were worsening of asthma, headache, and nasopharyngitis; most events were mild to moderate in severity.
Reslizumab improved lung function, asthma control and symptoms, and quality of life. It was well tolerated in patients with inadequately controlled asthma (despite standard therapy) and elevated blood eosinophil levels. Overall, the 3.0-mg/kg dose of reslizumab provided greater improvements in asthma outcomes vs the 0.3-mg/kg dose, with comparable safety.
ClinicalTrials.gov; No.: NCT01270464; URL: www.clinicaltrials.gov.
这项 3 期研究进一步描述了雷索利珠单抗(一种人源化抗 IL-5 单克隆抗体)在既往接受中至高剂量吸入性皮质类固醇治疗但仍控制不佳、且血嗜酸性粒细胞计数≥400 个/μL 的 12 至 75 岁哮喘患者中的疗效和安全性。
患者随机接受雷索利珠单抗 0.3 或 3.0mg/kg 或安慰剂,每 4 周 1 次,共 16 周(共 4 次)。主要终点为 16 周时支气管扩张剂前 FEV1 的基线变化。次要终点包括 FVC、用力呼出 25%至 75%肺活量时的流量(FEF)、患者报告的哮喘症状控制情况、短效β激动剂(SABA)使用、血嗜酸性粒细胞计数和安全性。
雷索利珠单抗治疗显著改善了 FEV1(与安慰剂相比,雷索利珠单抗 0.3 和 3.0mg/kg 组的差异分别为 115mL[95%CI,16-215;P=0.0237]和 160mL[95%CI,60-259;P=0.0018])和 FVC(130mL)及 FEF(233mL/s)的临床意义上的增加。雷索利珠单抗 3.0mg/kg 组患者的哮喘控制问卷(ACQ)和哮喘生命质量问卷(AQLQ)评分均有改善(3.0mg/kg 组的改善作用更显著;P<0.05)。AQLQ 达到了最小重要差异(雷索利珠单抗 3.0mg/kg),但 ACQ 未达到。哮喘症状效用指数和 SABA 使用评分也得到了改善。最常见的不良事件是哮喘恶化、头痛和鼻咽炎;大多数事件的严重程度为轻度至中度。
雷索利珠单抗改善了肺功能、哮喘控制和症状以及生活质量。在接受标准治疗但血嗜酸性粒细胞水平升高的控制不佳的哮喘患者中,雷索利珠单抗具有良好的耐受性。总体而言,3.0mg/kg 剂量的雷索利珠单抗与 0.3mg/kg 剂量相比,在改善哮喘结局方面具有更大的优势,安全性相当。
ClinicalTrials.gov;编号:NCT01270464;网址:www.clinicaltrials.gov。