Wahida Adam, Buschhorn Lars
Institute of Metabolism and Cell Death Ingolstädter Landstraße 1 85764 Neuherberg Germany.
National Center for Tumor Diseases (NCT) Heidelberg Division of Gynaecological Oncology Im Neuenheimer Feld 440 69120 Heidelberg Germany.
Med Genet. 2023 Dec 5;35(4):269-273. doi: 10.1515/medgen-2023-2064. eCollection 2023 Dec.
Monitoring ctDNA by liquid biopsies seems to represent the perfect match for precision oncology and its cornerstone clinical framework: the molecular tumour board (MTB). Detecting and scrutinising the success of targeted therapies or tracking and, for that matter, addressing the therapy with the evolutive nature of a tumour are some of the main advancements one considers to be important for the MTB. One challenge is correlating the estimated allele frequency of each identified genetic alteration determined by analysing the ctDNA sequencing results and matching these with the range of suitable drugs, which may limit the simultaneous treatment of all tumour variations. This limitation arises because a new biopsy would typically be required to evaluate the response to treatment. As a result, evaluating the success of MTB recommendations relies on traditional staging methods, highlighting an existing diagnostic gap. Thus, optimising liquid biopsy technology could enhance the efficacy of MTB treatment recommendations and ensuing tailored therapies. Herein, we discuss the prospect of ctDNA analyses in the molecular tumour board.
通过液体活检监测循环肿瘤DNA(ctDNA)似乎是精准肿瘤学及其基石临床框架——分子肿瘤委员会(MTB)的完美匹配。检测和审查靶向治疗的成效,或者追踪并应对具有不断演变特性的肿瘤的治疗,是人们认为对分子肿瘤委员会至关重要的一些主要进展。一个挑战是将通过分析ctDNA测序结果确定的每个已识别基因改变的估计等位基因频率进行关联,并将其与合适药物的范围相匹配,这可能会限制对所有肿瘤变异的同时治疗。这种限制的出现是因为通常需要进行新的活检来评估治疗反应。因此,评估分子肿瘤委员会建议的成效依赖于传统的分期方法,凸显了现有的诊断差距。因此,优化液体活检技术可以提高分子肿瘤委员会治疗建议及后续定制治疗的疗效。在此,我们讨论分子肿瘤委员会中ctDNA分析的前景。