Abrams Jeffrey, Conley Barbara, Mooney Margaret, Zwiebel James, Chen Alice, Welch John J, Takebe Naoko, Malik Shakun, McShane Lisa, Korn Edward, Williams Mickey, Staudt Louis, Doroshow James
From the Division of Cancer Treatment and Diagnosis, National Cancer Institute at the National Institutes of Health, Bethesda, MD; Center for Cancer Genomics, National Cancer Institute at the National Institutes of Health, Bethesda, MD; and Leidos Corporation, Frederick, MD.
Am Soc Clin Oncol Educ Book. 2014:71-6. doi: 10.14694/EdBook_AM.2014.34.71.
The promise of precision medicine will only be fully realized if the research community can adapt its clinical trials methodology to study molecularly characterized tumors instead of the traditional histologic classification. Such trials will depend on adequate tissue collection, availability of quality controlled, high throughput molecular assays, and the ability to screen large numbers of tumors to find those with the desired molecular alterations. The National Cancer Institute's (NCI) new National Clinical Trials Network (NCTN) is well positioned to conduct such trials. The NCTN has the ability to seamlessly perform ethics review, register patients, manage data, and deliver investigational drugs across its many sites including both in cities and rural communities, academic centers, and private practices. The initial set of trials will focus on different questions: (1) Exceptional Responders Initiative-why do a minority of patients with solid tumors or lymphoma respond very well to some drugs even if the majority do not?; (2) NCI MATCH trial-can molecular markers predict response to targeted therapies in patients with advanced cancer resistant to standard treatment?; (3) ALCHEMIST trial-will targeted epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) inhibitors improve survival for adenocarcinoma of the lung in the adjuvant setting?; and (4) Lung Cancer Master Protocol trial for advanced squamous cell lung cancer-is there an advantage to developing drugs for small subsets of molecularly characterized tumors in a single, multiarm trial design? These studies will hopefully spawn a new era of treatment trials that will carefully select the tumors that may respond best to investigational therapy.
只有当研究界能够调整其临床试验方法,以研究分子特征明确的肿瘤而非传统的组织学分类时,精准医学的前景才能完全实现。此类试验将依赖于充足的组织采集、质量可控的高通量分子检测方法的可用性,以及筛选大量肿瘤以找出具有所需分子改变的肿瘤的能力。美国国立癌症研究所(NCI)新的国家临床试验网络(NCTN)非常适合开展此类试验。NCTN有能力在其众多地点(包括城市和农村社区、学术中心及私人诊所)无缝进行伦理审查、登记患者、管理数据并提供研究药物。首批试验将聚焦于不同问题:(1)“特殊应答者倡议”——为什么少数实体瘤或淋巴瘤患者对某些药物反应非常好,即使大多数患者并非如此?;(2)NCI MATCH试验——分子标志物能否预测对标准治疗耐药的晚期癌症患者对靶向治疗的反应?;(3)ALCHEMIST试验——在辅助治疗中,靶向表皮生长因子受体(EGFR)和间变性淋巴瘤激酶(ALK)抑制剂能否提高肺腺癌患者的生存率?;以及(4)晚期肺鳞状细胞癌的肺癌主方案试验——在单一的多臂试验设计中,为分子特征明确的肿瘤小亚群开发药物是否有优势?这些研究有望催生一个新的治疗试验时代,该时代将仔细挑选可能对研究性治疗反应最佳的肿瘤。