Pinczak Witold, Trzcińska Sylwia, Kamiński Mikołaj
Department of Medicine I, Poznan University of Medical Sciences, Poznań, Poland.
Provincial Hospital in Poznan, Poznań, Poland.
JMIR Form Res. 2022 Apr 21;6(4):e33893. doi: 10.2196/33893.
Cardiovascular diseases remain the leading cause of morbidity and mortality worldwide. Gene therapies (GTs) may become a novel therapeutic option for cardiovascular diseases.
We aimed to characterize all trials involving human subjects utilizing GT to treat noncongenital cardiovascular diseases.
In March 2021, we searched for clinical trials on the ClinicalTrials.gov (CT), International Clinical Trials Registry Platform (ICTRP), and International Standard Randomised Controlled Trials Number (ISRCTN) databases. Two authors screened the titles and registry notes of all the searched studies. We collected details of the included studies regarding their design, location funding source, treated conditions, completion, publication statuses, and final outcomes.
We generated a total of 3508 records, and 50 unique clinical trials met our eligibility criteria. Of these, 20 (40%) concerned peripheral artery disease, and 18 (36%) concerned coronary artery disease. Most studies were randomized (34/50, 68%) and were performed in multiple locations (30/50, 60%), and around half of the trials compared GT with a placebo (27/50, 54%), while one in four were single-arm (14/50, 28%), and the rest concerned dose-finding (22%). More than half of the trials (29/50, 58%) were funded by industry. Of the 50 clinical trials, 28 (56%) published their results by the data collection date (March 2021), and 22 of 31 (71%) were slated to be completed before 2021. Overall, 12 of 28 (42.9%) clinical trials showed favorable outcomes of the intervention.
Among noncongenital cardiovascular diseases, GTs are mostly investigated in peripheral artery disease and coronary artery disease. Many clinical trials on GT use in noncongenital cardiovascular diseases did not disclose their results. Regardless of the trial phase, less than half of published studies on GT in noncongenital cardiovascular diseases showed promising results.
心血管疾病仍然是全球发病和死亡的主要原因。基因疗法(GTs)可能成为心血管疾病的一种新型治疗选择。
我们旨在对所有涉及利用基因疗法治疗非先天性心血管疾病的人体试验进行特征描述。
2021年3月,我们在ClinicalTrials.gov(CT)、国际临床试验注册平台(ICTRP)和国际标准随机对照试验编号(ISRCTN)数据库中搜索临床试验。两名作者筛选了所有检索到的研究的标题和注册说明。我们收集了纳入研究的详细信息,包括其设计、地点、资金来源、治疗疾病、完成情况、发表状态和最终结果。
我们共获得3508条记录,50项独特的临床试验符合我们的纳入标准。其中,20项(40%)涉及外周动脉疾病,18项(36%)涉及冠状动脉疾病。大多数研究是随机的(34/50,68%),且在多个地点进行(30/50,60%),约一半的试验将基因疗法与安慰剂进行比较(27/50,54%),四分之一为单臂试验(14/50,28%),其余涉及剂量探索(22%)。超过一半的试验(29/50,58%)由行业资助。在50项临床试验中,28项(56%)在数据收集日期(2021年3月)前发表了结果,31项中的22项(71%)预计在2021年前完成。总体而言,28项临床试验中有12项(42.9%)显示干预有良好结果。
在非先天性心血管疾病中,基因疗法主要在外周动脉疾病和冠状动脉疾病中进行研究。许多关于基因疗法用于非先天性心血管疾病的临床试验未公布其结果。无论试验阶段如何,在非先天性心血管疾病中发表的关于基因疗法的研究中,不到一半显示出有前景的结果。