Department of Medicine, University of Western Ontario, London, ON, Canada.
Department of Epidemiology and Biostatistics, University of Western Ontario, London, ON, Canada.
Inflamm Bowel Dis. 2018 Sep 15;24(10):2155-2164. doi: 10.1093/ibd/izy117.
As knowledge of the pathogenesis of inflammatory bowel disease (IBD) has grown, many new medical therapies have become available. Evaluation of the efficacy and safety of new drugs has conventionally been established with placebo-controlled randomized trials. However, given that highly effective and safe biologic agents such as tumor necrosis factor (TNF) antagonists, vedolizumab, and ustekinumab are currently available, the continued use of placebo-controlled studies to evaluate new molecules should be questioned. Although alternate study designs are available, their implementation presents multiple challenges that need to be overcome. Other challenges in the current investigative landscape include poor recruitment rates, enrollment of highly refractory patients, and substantial changes in the regulatory standards required for drug approval. In this article, we present an overview of these challenges and discuss potential solutions with an emphasis on implications for the practicing clinician.
随着对炎症性肠病(IBD)发病机制的认识不断提高,许多新的医学治疗方法已经问世。新药物的疗效和安全性评估通常采用安慰剂对照随机试验来确立。然而,鉴于目前已有像肿瘤坏死因子(TNF)拮抗剂、vedolizumab 和 ustekinumab 等高效且安全的生物制剂,继续使用安慰剂对照研究来评估新分子应该受到质疑。尽管有其他替代的研究设计可用,但它们的实施存在许多需要克服的挑战。当前研究领域中的其他挑战包括招募率低、招募难治性患者以及药物批准所需的监管标准发生重大变化。在本文中,我们将介绍这些挑战的概述,并讨论潜在的解决方案,重点强调对临床医生的影响。