Haselmann Verena, Hedtke Maren, Neumaier Michael
Institute of Clinical Chemistry, University Medicine Mannheim, Medical Faculty Mannheim, University of Heidelberg, 68167 Mannheim, Germany.
Diagnostics (Basel). 2022 Mar 19;12(3):748. doi: 10.3390/diagnostics12030748.
Circulating tumor DNA (ctDNA), accurately described by the term liquid profiling (LP), enables real-time assessment of the tumor mutational profile as a minimally invasive test and has therefore rapidly gained traction, particular for the management of cancer patients. By LP, tumor-specific genetic alterations can be determined as part of companion diagnostics to guide selection of appropriate targeted therapeutics. Because LP facilitates longitudinal monitoring of cancer patients, it can be used to detect acquired resistant mechanisms or as a personalized biomarker for earlier detection of disease recurrence, among other applications. However, LP is not yet integrated into routine care to the extent that might be expected. This is due to the lack of harmonization and standardization of preanalytical and analytical workflows, the lack of proper quality controls, limited evidence of its clinical utility, heterogeneous study results, the uncertainty of clinicians regarding the value and appropriate indications for LP and its interpretation, and finally, the lack of reimbursement for most LP tests. In this review, the value proposition of LP for cancer patient management and treatment optimization, the current status of implementation in standard care, and the main challenges that need to be overcome are discussed in detail.
循环肿瘤DNA(ctDNA),用术语液体活检(LP)来准确描述,作为一种微创检测方法,能够对肿瘤突变谱进行实时评估,因此迅速受到关注,尤其在癌症患者管理方面。通过液体活检,可以确定肿瘤特异性基因改变,作为伴随诊断的一部分,以指导选择合适的靶向治疗药物。由于液体活检有助于对癌症患者进行纵向监测,它可用于检测获得性耐药机制,或作为个性化生物标志物用于更早地检测疾病复发等。然而,液体活检尚未达到预期的常规应用程度。这是由于分析前和分析工作流程缺乏协调和标准化、缺乏适当的质量控制、其临床效用的证据有限、研究结果参差不齐、临床医生对液体活检的价值、适当适应症及其解读存在不确定性,以及最后,大多数液体活检检测缺乏报销。在本综述中,将详细讨论液体活检在癌症患者管理和治疗优化方面的价值主张、在标准治疗中的实施现状以及需要克服的主要挑战。