Cheng Lu, Yang Tianrui, Ma Xiang, Han Yuling, Wang Yongtai
Department of Respiratory Medicine, Jinan Children's Hospital, Jinan, China.
Ben and Maytee Fisch College of Pharmacy, 23534University of Texas at Tyler, Tyler, TX, USA.
J Pharm Pract. 2023 Apr;36(2):370-382. doi: 10.1177/08971900211038251. Epub 2021 Aug 12.
Omalizumab is currently approved for the treatment of moderate-to-severe allergic asthma in patients 6 years and older. To assess the effectiveness and safety of subcutaneous omalizumab as an add-on therapy option for moderate-severe allergic asthma in patients aged 6-20 years old. The studies published from July, 1970 to May, 2021 were searched from the electronic databases which followed keywords: ("anti-IgE" OR "anti-immunoglobulin E" OR "anti-IgE antibody" OR "omalizumab" OR "rhuMAb-E25" OR "Xolair") AND "asthma" AND ("child" OR "children" OR "adolescents" OR "youth" OR "teenager" OR "kids" OR "pediatric"). Thirteen studies were pooled to determine the effectiveness and safety of omalizumab. Efficacy endpoints were evaluated using a fixed-effects model or a random-effects model depending on heterogeneity. Safety endpoints were evaluated by odds ratio. Thirteen studies were included. In this meta-analysis, our results showed that fractional exhaled nitric oxide and asthma control test scores were significantly improved with omalizumab treatment. Serum immunoglobulin E was also decreased in children with moderate-to-severe asthma after treatment with omalizumab. The analysis found that there was no significant difference between pre-and post-treatment in forced expiratory volume in one second/ forced vital capacity ratio, forced expiratory flow between 25 and 75% of vital capacity, or FEV1. Overall, more adverse events occurred with omalizumab compared to placebo. However, the degree was mild to moderate. This meta-analysis indicates that omalizumab is safe and effective to treat children and adolescents with moderate-to-severe asthma.
奥马珠单抗目前被批准用于治疗6岁及以上的中重度过敏性哮喘患者。评估皮下注射奥马珠单抗作为6 - 20岁中重度过敏性哮喘附加治疗方案的有效性和安全性。检索1970年7月至2021年5月发表的研究,电子数据库遵循的关键词为:(“抗IgE”或“抗免疫球蛋白E”或“抗IgE抗体”或“奥马珠单抗”或“重组人源化抗IgE单克隆抗体E25”或“Xolair”)以及“哮喘”以及(“儿童”或“孩子们”或“青少年”或“青年”或“青少年”或“儿童”或“儿科”)。汇总了13项研究以确定奥马珠单抗的有效性和安全性。根据异质性,使用固定效应模型或随机效应模型评估疗效终点。通过比值比评估安全性终点。纳入了13项研究。在这项荟萃分析中,我们的结果表明,奥马珠单抗治疗可显著改善呼出一氧化氮分数和哮喘控制测试分数。奥马珠单抗治疗后,中重度哮喘患儿的血清免疫球蛋白E也有所降低。分析发现,治疗前后一秒用力呼气量/用力肺活量比值、肺活量25%至75%之间的用力呼气流量或第一秒用力呼气量无显著差异。总体而言,与安慰剂相比,奥马珠单抗发生的不良事件更多。然而,程度为轻度至中度。这项荟萃分析表明,奥马珠单抗治疗儿童和青少年中重度哮喘是安全有效的。