Joffe Erel, Iasonos Alexia, Younes Anas
All authors: Memorial Sloan Kettering Cancer Center, New York, NY.
J Clin Oncol. 2017 Mar 20;35(9):1011-1017. doi: 10.1200/JCO.2016.70.8891. Epub 2017 Feb 13.
Personalization of therapy to target specific molecular pathways has been placed in the forefront of cancer research. Initial reports from clinical trials designed to select patients for appropriate treatment on the basis of tumor characteristics not only have generated considerable excitement but also have identified several challenges. These challenges include the overcoming of regulatory and logistic difficulties, identification of the best selection biomarkers and diagnostic platforms that can be applied in the clinical setting, definition of relevant outcomes in small preselected patient populations, and the design of methods that facilitate rapid enrollment and interpretation of clinical trials by aggregating data across histologically diverse malignancies with common genetic alterations. Furthermore, because our knowledge of the functional consequences of many genetic alterations lags, investigators and sponsors struggle with choosing between ideal clinical trial designs and more practical ones. These challenges are amplified when more than one biomarker is used to select patients for a combination of targeted agents. This review summarizes the current status and challenges of clinical trials in the genomic era and proposes ways to address these challenges.
针对特定分子途径进行个性化治疗已成为癌症研究的前沿领域。旨在根据肿瘤特征为患者选择合适治疗方案的临床试验初步报告不仅引发了极大的关注,也发现了一些挑战。这些挑战包括克服监管和后勤方面的困难、确定可应用于临床环境的最佳选择生物标志物和诊断平台、在预先选定的小患者群体中定义相关结果,以及设计通过汇总具有共同基因改变的组织学不同恶性肿瘤的数据来促进临床试验快速入组和解读的方法。此外,由于我们对许多基因改变的功能后果的了解滞后,研究人员和申办者在理想的临床试验设计和更实际的设计之间难以抉择。当使用一种以上生物标志物为联合靶向药物选择患者时,这些挑战会更加突出。本综述总结了基因组时代临床试验的现状和挑战,并提出了应对这些挑战的方法。