Olmedillas-López Susana, Olivera-Salazar Rocío, García-Arranz Mariano, García-Olmo Damián
New Therapies Laboratory, Health Research Institute-Fundación Jiménez Díaz University Hospital (IIS-FJD), Avda. Reyes Católicos, 2, 28040, Madrid, Spain.
Department of Surgery, School of Medicine, Universidad Autónoma de Madrid (UAM), 28029, Madrid, Spain.
Mol Diagn Ther. 2022 Jan;26(1):61-87. doi: 10.1007/s40291-021-00562-2. Epub 2021 Nov 13.
In the era of personalized medicine and targeted therapies for the management of patients with cancer, ultrasensitive detection methods for tumor genotyping, such as next-generation sequencing or droplet digital polymerase chain reaction (ddPCR), play a significant role. In the search for less invasive strategies for diagnosis, prognosis and disease monitoring, the number of publications regarding liquid biopsy approaches using ddPCR has increased substantially in recent years. There is a long list of malignancies in which ddPCR provides a reliable and accurate tool for detection of nucleic acid-based markers derived from cell-free DNA, cell-free RNA, circulating tumor cells, extracellular vesicles or exosomes when isolated from whole blood, plasma and serum, helping to anticipate tumor relapse or unveil intratumor heterogeneity and clonal evolution in response to treatment. This updated review describes recent developments in ddPCR platforms and provides a general overview about the major applications of liquid biopsy in blood, including its utility for molecular response and minimal residual disease monitoring in hematological malignancies or the therapeutic management of patients with colorectal or lung cancer, particularly for the selection and monitoring of treatment with tyrosine kinase inhibitors. Although plasma is the main source of genetic material for tumor genomic profiling, liquid biopsy by ddPCR is being investigated in a wide variety of biologic fluids, such as cerebrospinal fluid, urine, stool, ocular fluids, sputum, saliva, bronchoalveolar lavage, pleural effusion, mucin, peritoneal fluid, fine needle aspirate, bile or pancreatic juice. The present review focuses on these "alternative" sources of genetic material and their analysis by ddPCR in different kinds of cancers.
在癌症患者管理的个性化医疗和靶向治疗时代,肿瘤基因分型的超灵敏检测方法,如下一代测序或液滴数字聚合酶链反应(ddPCR),发挥着重要作用。在寻找侵入性较小的诊断、预后和疾病监测策略的过程中,近年来关于使用ddPCR的液体活检方法的出版物数量大幅增加。有一长串恶性肿瘤,当从全血、血浆和血清中分离时,ddPCR为检测源自游离DNA、游离RNA、循环肿瘤细胞、细胞外囊泡或外泌体的基于核酸的标志物提供了可靠且准确的工具,有助于预测肿瘤复发或揭示肿瘤内异质性以及对治疗的克隆进化。这篇更新的综述描述了ddPCR平台的最新进展,并对液体活检在血液中的主要应用进行了概述,包括其在血液系统恶性肿瘤的分子反应和微小残留病监测或结直肠癌或肺癌患者的治疗管理中的效用,特别是在酪氨酸激酶抑制剂治疗的选择和监测方面。尽管血浆是肿瘤基因组分析的主要遗传物质来源,但通过ddPCR进行的液体活检正在多种生物体液中进行研究,如脑脊液、尿液、粪便、眼液、痰液、唾液、支气管肺泡灌洗液、胸腔积液、黏液、腹腔积液、细针穿刺抽吸物、胆汁或胰液。本综述重点关注这些“替代”遗传物质来源及其在不同类型癌症中通过ddPCR进行的分析。