Ghaemi S N, Selker Harry P
Mood Disorders Program, Department of Psychiatry, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA.
Tufts Clinical and Translational Scientific Institute, Tufts University, Boston, MA, USA.
J Clin Transl Sci. 2017 Jun;1(3):198-204. doi: 10.1017/cts.2017.2. Epub 2017 Jul 10.
Although classical randomized clinical trials (RCTs) are the gold standard for proof of drug efficacy, randomized discontinuation trials (RDTs), sometimes called "enriched" trials, are used increasingly, especially in psychiatric maintenance studies.
A narrative review of two decades of experience with RDTs.
RDTs in psychiatric maintenance trials tend to use a dependent variable as a predictor: treatment response. Treatment responders are assessed for treatment response. This tautology in the logic of RDTs renders them invalid, since the predictor and the outcome are the same variable. Although RDTs can be designed to avoid this tautologous state of affairs, like using independent predictors of outcomes, such is not the case with psychiatric maintenance studies Further, purported benefits of RDTs regarding feasibility were found to be questionable. Specifically, RDTs do not enhance statistical power in many settings, and, because of high dropout rates, produce results of questionable validity. Any claimed benefits come with notably reduced generalizability.
RDTs appear to be scientifically invalid as used in psychiatric maintenance designs. Their purported feasibility benefits are not seen in actual trials for psychotropic drugs. There is warrant for changes in federal policy regarding marketing indications for maintenance efficacy using the RDT design.
尽管经典随机临床试验(RCTs)是证明药物疗效的金标准,但随机撤药试验(RDTs),有时也被称为“富集”试验,正越来越多地被使用,尤其是在精神疾病维持治疗研究中。
对二十年来RDTs的经验进行叙述性综述。
精神疾病维持治疗试验中的RDTs倾向于将一个因变量用作预测指标:治疗反应。对治疗有反应者进行治疗反应评估。RDTs逻辑中的这种同义反复使其无效,因为预测指标和结果是同一个变量。尽管RDTs可以设计成避免这种同义反复的情况,比如使用结果的独立预测指标,但精神疾病维持治疗研究并非如此。此外,RDTs在可行性方面所谓的优势也被发现存在疑问。具体而言,RDTs在许多情况下并不能提高统计效力,而且由于高脱落率,其产生的结果有效性存疑。任何声称的优势都伴随着显著降低的可推广性。
在精神疾病维持治疗设计中使用的RDTs似乎在科学上是无效的。其在可行性方面所谓的优势在精神药物的实际试验中并未体现。有必要改变联邦政策中关于使用RDT设计进行维持疗效市场适应症的规定。