Hammond H K, McKirnan M D
San Diego VA Healthcare System, Department of Medicine, University of California (111A) 3350 La Jolla Village Drive, San Diego, CA 92161, USA.
Cardiovasc Res. 2001 Feb 16;49(3):561-7. doi: 10.1016/s0008-6363(00)00257-1.
The current published clinical literature on angiogenic gene therapy for the treatment of myocardial ischemia does not include a single randomized, placebo-controlled trial. Based on current clinical literature, it is an unproven therapy. Successful animal studies combined with published reports of good outcomes in patients enrolled in uncontrolled trials has led to the expectation that angiogenic gene therapy will ultimately become a clinical reality. The next important landmark in the field will be the publication of data showing a favorable effect of angiogenic gene transfer in placebo-controlled, blinded clinical trials.
目前已发表的关于血管生成基因疗法治疗心肌缺血的临床文献中,没有一项是随机、安慰剂对照试验。根据目前的临床文献,这是一种未经证实的疗法。成功的动物研究以及在非对照试验中入组患者取得良好结果的已发表报告,使得人们期望血管生成基因疗法最终能成为临床现实。该领域的下一个重要里程碑将是发表在安慰剂对照、双盲临床试验中显示血管生成基因转移具有积极效果的数据。