Bisig Bettina, Lefort Karine, Carras Sylvain, de Leval Laurence
Institute of Pathology, Department of Laboratory Medicine and Pathology, Lausanne University Hospital and Lausanne University, Lausanne, Switzerland.
Institute for Advanced Biosciences (INSERM U1209, CNRS UMR 5309, UGA), Department of Molecular Biology and Department of Oncohematology, University Hospital Grenoble and University Grenoble Alpes, Grenoble, France.
Hum Pathol. 2025 Feb;156:105679. doi: 10.1016/j.humpath.2024.105679. Epub 2024 Nov 2.
The analysis of circulating tumor DNA (ctDNA) in liquid biopsy specimens has an established role for the detection of predictive molecular alterations and acquired resistance mutations in several tumors. The low-invasiveness of this approach allows for repeated sampling and dynamic monitoring of disease evolution. Originating from the entire body tumor bulk, plasma-derived ctDNA reflects intra- and interlesional genetic heterogeneity. In the management of lymphoma patients, ctDNA quantification at various timepoints of the patient's clinical history is emerging as a complementary tool that may improve risk stratification, assessment of treatment response and early relapse detection during follow-up, most prominently in patients with diffuse large B-cell lymphoma or classic Hodgkin lymphoma. While liquid biopsies have not yet entered standard-of-care treatment protocols in these settings, several trials have provided evidence that at least a subset of lymphoma patients may benefit from the introduction of liquid biopsies into daily clinical care. In parallel, continuous technological developments have enabled highly sensitive ctDNA assessment methods, which span from locus-specific techniques identifying single hotspot mutations, to sequencing panels and genome-wide approaches that explore broader genetic and epigenetic alterations. Here, we provide an overview of current methods and ongoing technical developments for ctDNA evaluation. We also summarize the most important data from a selection of clinical studies that have explored the clinical use of ctDNA in several lymphoma entities.
对液体活检样本中的循环肿瘤DNA(ctDNA)进行分析,在检测多种肿瘤的预测性分子改变和获得性耐药突变方面已发挥既定作用。这种方法的低侵入性允许重复采样和动态监测疾病进展。源自全身肿瘤组织块的血浆源性ctDNA反映了肿瘤内和肿瘤间的遗传异质性。在淋巴瘤患者的管理中,在患者临床病程的不同时间点对ctDNA进行定量分析,正逐渐成为一种辅助工具,可改善风险分层、评估治疗反应以及在随访期间早期检测复发,这在弥漫性大B细胞淋巴瘤或经典霍奇金淋巴瘤患者中最为显著。虽然在这些情况下液体活检尚未纳入标准治疗方案,但多项试验已提供证据表明,至少一部分淋巴瘤患者可能会从将液体活检引入日常临床护理中获益。与此同时,持续的技术发展催生了高度灵敏的ctDNA评估方法,从识别单个热点突变的位点特异性技术,到探索更广泛遗传和表观遗传改变的测序板和全基因组方法。在此,我们概述了当前用于ctDNA评估的方法和正在进行的技术发展。我们还总结了一系列临床研究中的最重要数据,这些研究探讨了ctDNA在多种淋巴瘤实体中的临床应用。