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异体人脐带间充质干细胞治疗慢性阻塞性肺疾病(COPD):一项匹配病例对照、I/II 期临床试验研究方案。

Allogeneic human umbilical cord-derived mesenchymal stem/stromal cells for chronic obstructive pulmonary disease (COPD): study protocol for a matched case-control, phase I/II trial.

机构信息

Department of Research & Development, Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Heathcare System, Hanoi, Vietnam

Clinical Research Department, Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Viet Nam.

出版信息

BMJ Open. 2021 May 13;11(5):e045788. doi: 10.1136/bmjopen-2020-045788.

Abstract

INTRODUCTION

The global prevalence of chronic obstructive pulmonary disease (COPD) is increasing, and it has become a major public health burden worldwide, including in Vietnam. A large body of preclinical and clinical studies supports the safety of mesenchymal stem/stromal cells (MSCs) in the treatment of lung injury, including COPD. The aim of this trial is to investigate the safety and potential therapeutic efficacy of allogeneic administration of umbilical cord-derived MSCs (UC-MSCs) as a supplementary intervention in combination with standard COPD medication treatments in patients with moderate-to-severe COPD based on the Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2019 and Vietnam Ministry of Health's guidelines.

METHODS AND ANALYSIS

This matched case-control phase I/II trial is conducted at Vinmec Times City International Hospital, Hanoi, Vietnam between June 2020 and December 2021. In this study, 40 patients will be enrolled and assigned into two age-matched, gender-matched and COPD condition-matched groups, including a UC-MSC group and a control group. Both groups will receive standard COPD medication treatment based on the GOLD 2019 guidelines and the Vietnam Ministry of Health protocol. The UC-MSC group will receive two doses of thawed UC-MSC product with an intervention interval of 3 months. The primary outcome measures will include the incidence of prespecified administration-associated adverse events and serious adverse events. The efficacy will be evaluated based on the absolute changes in the number of admissions, arterial blood gas analysis, lung function and lung fibrosis via CT scan and chest X-ray. The clinical evaluation will be conducted at baseline and 3, 6 and 12 months postintervention.

ETHICS AND DISSEMINATION

Ethical approval was secured from the Ethical Committee of Vinmec International Hospital (number:166/2019/QĐ-VMEC) and Vietnam Ministry of Health (number:2002/QĐ-BYT). The results will be reported to trial collaborators, publication in peer-reviewed academic journals.

TRIAL REGISTRATION NUMBER

NCT04433104.

摘要

简介

慢性阻塞性肺疾病(COPD)在全球的患病率正在上升,它已成为全球范围内(包括越南)的主要公共卫生负担。大量的临床前和临床研究支持间充质干细胞(MSCs)在治疗肺损伤,包括 COPD 方面的安全性。本试验旨在根据全球倡议慢性阻塞性肺疾病(GOLD)2019 年和越南卫生部指南,调查同种异体脐带来源间充质干细胞(UC-MSCs)辅助治疗中重度 COPD 患者的安全性和潜在疗效。

方法和分析

这是一项在越南河内 Vinmec Times City 国际医院进行的匹配病例对照的 I/II 期试验,于 2020 年 6 月至 2021 年 12 月进行。本研究共纳入 40 例患者,并将其分为两组,即 UC-MSC 组和对照组,每组 20 例。两组患者均将接受基于 GOLD 2019 指南和越南卫生部方案的标准 COPD 药物治疗。UC-MSC 组将接受两次解冻的 UC-MSC 产品治疗,两次治疗间隔为 3 个月。主要观察指标将包括预定给药相关不良事件和严重不良事件的发生率。疗效将根据入院次数、动脉血气分析、肺功能和 CT 扫描及胸片的肺纤维化的绝对变化进行评估。临床评估将在基线和干预后 3、6 和 12 个月进行。

伦理和传播

本研究已获得 Vinmec 国际医院伦理委员会(编号:166/2019/QĐ-VMEC)和越南卫生部(编号:2002/QĐ-BYT)的伦理批准。研究结果将报告给试验合作方,并在同行评议的学术期刊上发表。

试验注册号

NCT04433104。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ae4/8126295/e3082d91b0f5/bmjopen-2020-045788f01.jpg

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