Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins University, Baltimore, MD.
Section of Medical Oncology, Rush Medical Center, Chicago, IL.
Clin Lung Cancer. 2020 Jul;21(4):295-307. doi: 10.1016/j.cllc.2020.02.008. Epub 2020 Feb 26.
Low rates of adult patient participation have been a persistent problem in cancer clinical trials and have continued to be a barrier to efficient drug development. The routine use of significant exclusion criteria has contributed to this problem by limiting participation in studies and creating significant clinical differences between the study cohorts and the real-world cancer patient populations. These routine exclusions also unnecessarily restrict opportunities for many patients to access potentially promising new therapies during clinical development. Multiple efforts are underway to broaden eligibility criteria, allowing more patients to enroll in studies and generating more robust data regarding the effect of novel therapies in the population at large. Focusing specifically on lung cancer as an example, a multistakeholder working group empaneled by the LUNGevity Foundation identified 14 restrictive and potentially outdated exclusion criteria that appear frequently in lung cancer clinical trials. As a part of the project, the group evaluated data from multiple recent lung cancer studies to ascertain the extent to which these 14 criteria appeared in study protocols and played a role in excluding patients (screen failures). The present report describes the working group's efforts to limit the use of these routine exclusions and presents clinical justifications for reducing the use of 14 criteria as routine exclusions in lung cancer studies, potentially expanding trial eligibility and improving the generalizability of the results from lung cancer trials.
成人患者参与率低一直是癌症临床试验中的一个长期存在的问题,也是药物开发效率的障碍。通过限制研究的参与和在研究队列与真实世界癌症患者人群之间产生显著的临床差异,常规使用重要的排除标准加剧了这一问题。这些常规排除也不必要地限制了许多患者在临床开发期间获得潜在有前途的新疗法的机会。目前正在进行多项努力来扩大合格标准,让更多的患者参与研究,并在更广泛的人群中生成关于新型疗法效果的更稳健数据。具体以肺癌为例,LUNGevity 基金会召集的一个多利益相关者工作组确定了 14 个常见的肺癌临床试验中存在的限制性和潜在过时的排除标准。作为该项目的一部分,该小组评估了多项最近的肺癌研究的数据,以确定这些 14 个标准在研究方案中的出现程度,并在排除患者(筛选失败)方面发挥作用。本报告描述了工作组限制这些常规排除的努力,并提出了减少肺癌研究中 14 个标准作为常规排除的临床依据,这可能会扩大试验资格,并提高肺癌试验结果的普遍性。