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单克隆抗体与传统常规二分法药物治疗慢性阻塞性肺疾病的疗效和安全性的网状Meta分析

Network meta-analysis of the efficacy and safety of monoclonal antibodies and traditional conventional dichotomous agents for chronic obstructive pulmonary disease.

作者信息

Xiong Yu, Hu Jia-Qiang, Tang Hui-Lin, Zhao Zhi-Xia, Liu Li-Hong

机构信息

Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

Department of Pharmacy, China-Japan Friendship Hospital, Beijing, China.

出版信息

Front Med (Lausanne). 2024 Feb 13;11:1334442. doi: 10.3389/fmed.2024.1334442. eCollection 2024.

DOI:10.3389/fmed.2024.1334442
PMID:38414617
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10898352/
Abstract

INTRODUCTION

Monoclonal antibodies (mAbs) against cytokines and chemokines or their receptors promise to be a potential therapeutic option to address chronic obstructive pulmonary disease (COPD). We aim to provide a comprehensive literature review of the improvement in FEV1 and safety when comparing mAbs with conventional dichotomous agents.

METHODS

We systematically searched 3 electronic databases (PubMed, EMBASE, and CENTRAL) up to August 1, 2023 to collect eligible randomized controlled trials (RCTs). A frequentist network meta-analysis using a random-effects model was deployed to calculate mean differences (MD) for FEV1, relative risk (RR) of treatment-emergent adverse events (TEAEs), and estimate the surface under cumulative rankings (SUCRA). A higher SUCRA indicates a better outcome.

RESULTS

This study included 23 RCTs involving a total of 20,853 patients. Overall, except for Dupilumab, mAbs did not significantly improve FEV1 compared to traditional conventional dichotomous agents. Among all the interventions included, Aclidinium bromide/Formoterol (AB/FF) (SUCRA 97.7%) ranked highest, followed by Umeclidinium/vilanterol (UMEC/VI) (SUCRA 93.5%), and Glycopyrrolate Formoterol Fumarate (GFF) (SUCRA 84.7%). Dupilumab (SUCRA 66.9%) ranked the fourth among all interventions but ranked the first among all the mAbs. Importantly, all mAbs demonstrated a good safety profile compared with placebo.

CONCLUSION

Considering the improvement in FEV1 and its safety, the development of mAbs for COPD still holds significant clinical potential.

SYSTEMATIC REVIEW REGISTRATION

PROSPERO, CRD42023452714.

摘要

引言

针对细胞因子、趋化因子及其受体的单克隆抗体(mAb)有望成为治疗慢性阻塞性肺疾病(COPD)的一种潜在选择。我们旨在全面综述单克隆抗体与传统二分法药物相比,在改善第1秒用力呼气容积(FEV1)和安全性方面的相关文献。

方法

我们系统检索了截至2023年8月1日的3个电子数据库(PubMed、EMBASE和CENTRAL),以收集符合条件的随机对照试验(RCT)。采用随机效应模型进行频率论网络荟萃分析,计算FEV1的平均差(MD)、治疗中出现的不良事件(TEAE)的相对风险(RR),并估计累积排名曲线下面积(SUCRA)。SUCRA值越高表明结果越好。

结果

本研究纳入23项RCT,共涉及20,853例患者。总体而言,除度普利尤单抗外,与传统二分法药物相比,单克隆抗体并未显著改善FEV1。在所有纳入的干预措施中,溴化阿地氯铵/福莫特罗(AB/FF)(SUCRA 97.7%)排名最高,其次是乌美溴铵/维兰特罗(UMEC/VI)(SUCRA 93.5%)和格隆溴铵富马酸福莫特罗(GFF)(SUCRA 84.7%)。度普利尤单抗(SUCRA 66.9%)在所有干预措施中排名第四,但在所有单克隆抗体中排名第一。重要的是,与安慰剂相比,所有单克隆抗体均显示出良好的安全性。

结论

考虑到FEV1的改善及其安全性,用于COPD的单克隆抗体的研发仍具有显著的临床潜力。

系统评价注册

PROSPERO,CRD42023452714。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/306a/10898352/51fdca9e4e83/fmed-11-1334442-g006.jpg
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