From the Icahn School of Medicine at Mount Sinai, New York, NY.
Division of Cancer Treatment and Diagnosis, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Cancer J. 2019 Jul/Aug;25(4):245-253. doi: 10.1097/PPO.0000000000000386.
Oncologic phase II trials that evaluate the activity of new therapeutic agents have evolved dramatically over the past 50 years. The standard approach beginning in the late 1960s focused on individual studies that evaluated new anticancer agents against a wide range of both solid and hematopoietic malignancies often in a single "broad phase II trial" that included hundreds of patients; such studies efficiently established the landscape for subsequent development of a specific drug with respect to likely disease focus, toxicity, dose, and schedule. In the 1980s and 1990s, emphasis on histological context drove an explosion in the number of individual phase II trials conducted; despite this increase in trial activity, investigations based on histology per se failed to improve the success rate of new agents brought to the clinic. Over the past 20 years, evolution toward a molecular drug development paradigm has demonstrably improved our ability to select patients more likely to benefit from systemic treatment; simultaneously, technological advances have permitted initial attempts at the rapid assignment of therapy based on predefined molecular characteristics of tumor or germline in broad-based master protocols that are inclusive of many diseases and molecularly characterized disease subsets, akin to but much more sophisticated scientifically than the broad phase II platforms of the past.
在过去的 50 年中,评估新治疗药物活性的肿瘤学 II 期临床试验发生了巨大变化。从 20 世纪 60 年代末开始,标准方法侧重于评估新抗癌药物对广泛的实体瘤和血液恶性肿瘤的活性的个别研究,通常在一个包含数百名患者的单一“广泛 II 期试验”中进行;这些研究有效地确定了后续特定药物开发的前景,包括可能的疾病焦点、毒性、剂量和方案。在 20 世纪 80 年代和 90 年代,对组织学背景的重视推动了大量个别 II 期临床试验的开展;尽管试验活动增加了,但基于组织学本身的研究并没有提高新药物在临床上的成功率。在过去的 20 年中,向分子药物开发范式的发展显然提高了我们选择更有可能从系统治疗中受益的患者的能力;同时,技术进步使得最初可以根据肿瘤或种系的预先定义的分子特征在广泛的主方案中快速分配治疗,这些方案包括许多疾病和分子特征疾病亚组,类似于但在科学上比过去的广泛的 II 期平台更加复杂。