临床荟萃 ›› 2023, Vol. 38 ›› Issue (10): 869-877.doi: 10.3969/j.issn.1004-583X.2023.10.001
• 循证研究 • 下一篇
收稿日期:2023-04-20
出版日期:2023-10-20
发布日期:2024-01-03
通讯作者:
阮俊文
E-mail:ruanjunwen2020@163.com
基金资助:
Ruan Junwen1(
), Zhou Jianrong2, Liu Weiyou2, Yuan Xiaoliang2, Yan Hao3
Received:2023-04-20
Online:2023-10-20
Published:2024-01-03
Contact:
Ruan Junwen
E-mail:ruanjunwen2020@163.com
摘要: 目的 系统评价度普利尤单抗治疗支气管哮喘的临床疗效和安全性。 方法 检索中国期刊全文数据库(CNKI)、万方数据库(Wanfang Database)、维普数据库(VIP)、中国生物医学文献数据库(CBM)、Cochrane Library、PubMed、Embase、Web of Science等数据库,检索时间为建库至2023年2月20日,纳入度普利尤单抗治疗支气管哮喘患者的随机对照试验(RCT),使用RevMan5.4软件进行Meta分析。结果 总纳入11项RCTs,共3759例患者,Meta分析结果显示,试验组哮喘急性加重人数[RR=0.48, 95%CI (0.40, 0.57), P<0.01]、哮喘控制问卷评分(Asthma control questionnaire, ACQ)[MD =-0.32, 95%CI (-0.43, -0.21), P<0.01]均少于对照组,试验组第1秒用力呼气容积(Forced expiratory volume in 1s, FEV1)[MD =0.51, 95%CI (0.31, 0.71), P<0.01]、哮喘生活质量问卷评分(Asthma quality of life questionnaire, AQLQ)[MD =0.32, 95%CI (0.20, 0.44), P<0.01]均高于对照组,差异有统计学意义(P<0.05);在血液嗜酸性粒细胞数<300/μl的哮喘人数[RR=1.10, 95%CI (0.93, 1.31), P=0.26]、不良事件[RR=1.03, 95%CI (0.98, 1.08), P=0.22]、严重不良事件[RR=1.21, 95%CI (0.86, 1.71), P=0.28]等方面,两组基本一致,差异无统计学意义(P>0.05)。结论 度普利尤单抗可有效减少哮喘急性加重人数、改善肺功能和提高患者的生活质量,且有较好的安全性。
中图分类号:
阮俊文, 周建荣, 刘惟优, 袁小亮, 颜颢. 度普利尤单抗治疗支气管哮喘疗效和安全性的meta分析[J]. 临床荟萃, 2023, 38(10): 869-877.
Ruan Junwen, Zhou Jianrong, Liu Weiyou, Yuan Xiaoliang, Yan Hao. Meta-analysis of the efficacy and safety of dupilumab on the treatment of bronchial asthma[J]. Clinical Focus, 2023, 38(10): 869-877.
| 纳入研究 | 病例数 | 平均年龄(岁) | 干预措施 | 疗程 | 结局指标 | ||||
|---|---|---|---|---|---|---|---|---|---|
| T/C | T | C | T | C | |||||
| Bacharier 2021[ | 273/135 | 8.9±1.6 | 9.0±1.6 | 达必妥100 mg q2w(W≤30kg), 200 mg q2w(W>30kg) | 安慰剂q2w | 52w | ①②③④⑥⑦ | ||
| Busse(a) 2018[ | 634/317 | ≥12 | 达必妥200 mg q2w | 安慰剂q2w | 52w | ② | |||
| Busse(b) 2018[ | 634/317 | ≥12 | 达必妥300 mg q2w | 安慰剂q2w | 52w | ② | |||
| Domingo 2022[ | 103/107 | 52.9±12.6 | 50.3±12.6 | 达必妥300 mg q2w | 安慰剂q2w | 24w | ①②④⑥ | ||
| Rabe 2018[ | 103/107 | 51.9±12.5 | 50.7±12.8 | 达必妥300 mg q2w | 安慰剂q2w | 24w | ①②③⑥⑦ | ||
| Wechsler 2021[ | 75/74 | 51.3±12.7 | 47.0±11.4 | 达必妥300 mg q2w | 安慰剂q2w | 12w | ①②③④⑤⑥⑦ | ||
| Wenzel(a) 2016[ | 150/158 | 48.6±13.0 | 达必妥200 mg q2w | 安慰剂q2w | 24w | ①②④⑤⑥⑦ | |||
| Wenzel(b) 2016[ | 154/158 | 48.6±13.0 | 达必妥200 mg q4w | 安慰剂q4w | 24w | ①②④⑤⑥⑦ | |||
| Wenzel(c) 2016[ | 157/158 | 48.6±13.0 | 达必妥300 mg q2w | 安慰剂q2w | 24w | ①②④⑤⑥⑦ | |||
| Wenzel(d) 2016[ | 157/158 | 48.6±13.0 | 达必妥300 mg q4w | 安慰剂q4w | 24w | ①②④⑤⑥⑦ | |||
| Wenzel 2013[ | 52/52 | 37.8±13.2 | 41.6±13.1 | 达必妥300 mg qw | 安慰剂qw | 12w | ①④⑥⑦ | ||
表1 纳入研究的基本特征
Tab.1 Basic characteristics of included studies
| 纳入研究 | 病例数 | 平均年龄(岁) | 干预措施 | 疗程 | 结局指标 | ||||
|---|---|---|---|---|---|---|---|---|---|
| T/C | T | C | T | C | |||||
| Bacharier 2021[ | 273/135 | 8.9±1.6 | 9.0±1.6 | 达必妥100 mg q2w(W≤30kg), 200 mg q2w(W>30kg) | 安慰剂q2w | 52w | ①②③④⑥⑦ | ||
| Busse(a) 2018[ | 634/317 | ≥12 | 达必妥200 mg q2w | 安慰剂q2w | 52w | ② | |||
| Busse(b) 2018[ | 634/317 | ≥12 | 达必妥300 mg q2w | 安慰剂q2w | 52w | ② | |||
| Domingo 2022[ | 103/107 | 52.9±12.6 | 50.3±12.6 | 达必妥300 mg q2w | 安慰剂q2w | 24w | ①②④⑥ | ||
| Rabe 2018[ | 103/107 | 51.9±12.5 | 50.7±12.8 | 达必妥300 mg q2w | 安慰剂q2w | 24w | ①②③⑥⑦ | ||
| Wechsler 2021[ | 75/74 | 51.3±12.7 | 47.0±11.4 | 达必妥300 mg q2w | 安慰剂q2w | 12w | ①②③④⑤⑥⑦ | ||
| Wenzel(a) 2016[ | 150/158 | 48.6±13.0 | 达必妥200 mg q2w | 安慰剂q2w | 24w | ①②④⑤⑥⑦ | |||
| Wenzel(b) 2016[ | 154/158 | 48.6±13.0 | 达必妥200 mg q4w | 安慰剂q4w | 24w | ①②④⑤⑥⑦ | |||
| Wenzel(c) 2016[ | 157/158 | 48.6±13.0 | 达必妥300 mg q2w | 安慰剂q2w | 24w | ①②④⑤⑥⑦ | |||
| Wenzel(d) 2016[ | 157/158 | 48.6±13.0 | 达必妥300 mg q4w | 安慰剂q4w | 24w | ①②④⑤⑥⑦ | |||
| Wenzel 2013[ | 52/52 | 37.8±13.2 | 41.6±13.1 | 达必妥300 mg qw | 安慰剂qw | 12w | ①④⑥⑦ | ||
图12 统计学意义分析图 注:“P<0.00001”取值为“P=0.00001”;在“FEV1”、“AQLQ”、“严重不良事件”中,均存在两项相同大权重研究,在去掉两项相同大权重研究后,所得P值为“0.0006/0.0007”、“<0.0001/<0.00001”、“0.44/0.63”,图中P取值为“0.0007”、“<0.0001”、“0.44”
Fig.12 Analytical graph of statistical significance
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