Lalu Manoj M, Sullivan Katrina J, Mei Shirley Hj, Moher David, Straus Alexander, Fergusson Dean A, Stewart Duncan J, Jazi Mazen, MacLeod Malcolm, Winston Brent, Marshall John, Hutton Brian, Walley Keith R, McIntyre Lauralyn
Department of Anesthesiology and Pain Medicine, The Ottawa Hospital, Ottawa, Canada.
Clinical Epidemiology Program, The Ottawa Hospital Research Institute, Ottawa, Canada.
Elife. 2016 Nov 17;5:e17850. doi: 10.7554/eLife.17850.
Evaluation of preclinical evidence prior to initiating early-phase clinical studies has typically been performed by selecting individual studies in a non-systematic process that may introduce bias. Thus, in preparation for a first-in-human trial of mesenchymal stromal cells (MSCs) for septic shock, we applied systematic review methodology to evaluate all published preclinical evidence. We identified 20 controlled comparison experiments (980 animals from 18 publications) of sepsis models. Meta-analysis demonstrated that MSC treatment of preclinical sepsis significantly reduced mortality over a range of experimental conditions (odds ratio 0.27, 95% confidence interval 0.18-0.40, latest timepoint reported for each study). Risk of bias was unclear as few studies described elements such as randomization and no studies included an appropriately calculated sample size. Moreover, the presence of publication bias resulted in a ~30% overestimate of effect and threats to validity limit the strength of our conclusions. This novel prospective application of systematic review methodology serves as a template to evaluate preclinical evidence prior to initiating first-in-human clinical studies.
在启动早期临床研究之前,对临床前证据的评估通常是通过非系统的过程选择个别研究来进行的,这可能会引入偏差。因此,在准备进行间充质基质细胞(MSC)用于感染性休克的首次人体试验时,我们应用系统评价方法来评估所有已发表的临床前证据。我们确定了20项关于脓毒症模型的对照比较实验(来自18篇出版物的980只动物)。荟萃分析表明,在一系列实验条件下,临床前脓毒症的MSC治疗显著降低了死亡率(优势比0.27,95%置信区间0.18 - 0.40,每个研究报告的最晚时间点)。由于很少有研究描述随机化等要素且没有研究包含适当计算的样本量,偏差风险尚不清楚。此外,发表偏倚的存在导致效应高估约30%,对有效性的威胁限制了我们结论的力度。这种系统评价方法的新颖前瞻性应用为在启动首次人体临床研究之前评估临床前证据提供了一个模板。