Philip G, Malmstrom K, Hampel F C, Weinstein S F, LaForce C F, Ratner P H, Malice M-P, Reiss T F
Merck & Co., Inc., Rahway, New Jersey, USA.
Clin Exp Allergy. 2002 Jul;32(7):1020-8. doi: 10.1046/j.1365-2222.2002.01422.x.
Cysteinyl leukotrienes are important proinflammatory mediators believed to have a role in allergic rhinitis.
This multicentre, randomized, double-blind, placebo- and active-controlled trial evaluated the effectiveness and tolerability of montelukast, a cysteinyl leukotriene receptor antagonist, for treating patients with seasonal allergic rhinitis.
After a 3- to 5-day, single-blind placebo run-in period, 1302 male and female patients (aged 15-81 years) with active allergic rhinitis symptoms were randomly assigned to receive montelukast 10 mg (n = 348), loratadine 10 mg (n = 602), or placebo (n = 352) administered once daily at bedtime for 2 weeks during the spring allergy season.
Mean patient characteristics and symptom scores at baseline were similar for the three treatment groups. The primary end-point, daytime nasal symptoms score (mean of nasal congestion, rhinorrhea, nasal pruritus, and sneezing scores; 0-3 scale), improved from baseline during treatment by (least squares mean, 95% confidence interval) - 0.37 (- 0.43, - 0.31), - 0.47 (- 0.52, - 0.43), and - 0.24 (- 0.29, - 0.18) in the montelukast, loratadine, and placebo groups, respectively (P < or = 0.001 comparing each active treatment with placebo). Mean changes from baseline in all other diary-based scores, including night-time and eye symptom scores, were significantly greater for each active treatment than for placebo. The rhinoconjunctivitis quality of life overall score improved significantly with montelukast and with loratadine as compared with placebo. Montelukast and loratadine showed a safety profile comparable to that of placebo.
Montelukast is well tolerated and provides improvements in daytime and night-time symptoms, as well as quality of life parameters, for patients with seasonal allergic rhinitis.
半胱氨酰白三烯是重要的促炎介质,被认为在过敏性鼻炎中起作用。
这项多中心、随机、双盲、安慰剂对照和活性药物对照试验评估了半胱氨酰白三烯受体拮抗剂孟鲁司特治疗季节性过敏性鼻炎患者的有效性和耐受性。
在进行3至5天的单盲安慰剂导入期后,1302例有活动性过敏性鼻炎症状的男性和女性患者(年龄15 - 81岁)被随机分配接受孟鲁司特10毫克(n = 348)、氯雷他定10毫克(n = 602)或安慰剂(n = 352),在春季过敏季节期间于睡前每日服用一次,持续2周。
三个治疗组在基线时的平均患者特征和症状评分相似。主要终点,白天鼻部症状评分(鼻塞、流涕、鼻痒和打喷嚏评分的平均值;0 - 3分制),在治疗期间与基线相比的改善情况(最小二乘均值,95%置信区间)分别为:孟鲁司特组 - 0.37(- 0.43,-
0.31)、氯雷他定组 - 0.47(- 0.52,- 0.43)和安慰剂组 - 0.24(- 0.29,- 0.18)(将每种活性药物治疗与安慰剂比较,P≤0.001)。所有其他基于日记的评分从基线的平均变化,包括夜间和眼部症状评分,每种活性药物治疗均显著大于安慰剂。与安慰剂相比,孟鲁司特和氯雷他定使鼻结膜炎生活质量总体评分显著改善。孟鲁司特和氯雷他定的安全性与安慰剂相当。
孟鲁司特耐受性良好,可为季节性过敏性鼻炎患者改善白天和夜间症状以及生活质量参数。