From the Leidos Biomedical Research Inc, Molecular Characterization Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD.
Cancer J. 2019 Jul/Aug;25(4):264-271. doi: 10.1097/PPO.0000000000000385.
The ability of next-generation sequencing (NGS) to comprehensively assess the molecular profile of a tumor specimen has transformed the clinical testing landscape in oncology. Accordingly, recent years have seen broad uptake of clinical NGS to inform cancer patient management. However, significant challenges remain. The annotation and clinical interpretation of variants identified by NGS tests often require rigorous review and may vary between laboratories. While a clearer regulatory path has emerged, reimbursement for NGS tests remains a subject of continuing debate. Basket clinical studies such as the National Cancer Institute Molecular Analysis of Therapy Choice are evaluating the degree to which matching of a targeted therapy to tumor molecular profile by NGS can be applied independently of tissue histology. Newer applications of NGS such as for circulating tumor DNA testing and to identify novel RNA fusion driver events continue to expand its clinical utility.
下一代测序(NGS)全面评估肿瘤标本分子谱的能力改变了肿瘤学领域的临床检测格局。因此,近年来,临床 NGS 已广泛用于癌症患者管理。然而,仍然存在重大挑战。NGS 测试鉴定的变异的注释和临床解释通常需要严格审查,并且可能因实验室而异。虽然更清晰的监管途径已经出现,但 NGS 测试的报销仍然是一个持续争论的问题。篮子临床研究,如美国国家癌症研究所的治疗选择的分子分析,正在评估通过 NGS 进行靶向治疗与肿瘤分子谱匹配的程度,是否可以独立于组织组织学进行。NGS 的新应用,如循环肿瘤 DNA 检测和鉴定新型 RNA 融合驱动事件,继续扩大其临床应用。