Bronkhorst Abel J, Holdenrieder Stefan
Technical University Munich Munich Biomarker Research Center, Institute of Laboratory Medicine, German Heart Center Lazarettstr. 36 80636 Munich Germany.
Med Genet. 2023 Dec 5;35(4):201-235. doi: 10.1515/medgen-2023-2065. eCollection 2023 Dec.
Liquid biopsies, in particular the profiling of circulating tumor DNA (ctDNA), have long held promise as transformative tools in cancer precision medicine. Despite a prolonged incubation phase, ctDNA profiling has recently experienced a strong wave of development and innovation, indicating its imminent integration into the cancer management toolbox. Various advancements in mutation-based ctDNA analysis methodologies and technologies have greatly improved sensitivity and specificity of ctDNA assays, such as optimized preanalytics, size-based pre-enrichment strategies, targeted sequencing, enhanced library preparation methods, sequencing error suppression, integrated bioinformatics and machine learning. Moreover, research breakthroughs have expanded the scope of ctDNA analysis beyond hotspot mutational profiling of plasma-derived apoptotic, mono-nucleosomal ctDNA fragments. This broader perspective considers alternative genetic features of cancer, genome-wide characterization, classical and newly discovered epigenetic modifications, structural variations, diverse cellular and mechanistic ctDNA origins, and alternative biospecimen types. These developments have maximized the utility of ctDNA, facilitating landmark research, clinical trials, and the commercialization of ctDNA assays, technologies, and products. Consequently, ctDNA tests are increasingly recognized as an important part of patient guidance and are being implemented in clinical practice. Although reimbursement for ctDNA tests by healthcare providers still lags behind, it is gaining greater acceptance. In this work, we provide a comprehensive exploration of the extensive landscape of ctDNA profiling methodologies, considering the multitude of factors that influence its development and evolution. By illuminating the broader aspects of ctDNA profiling, the aim is to provide multiple entry points for understanding and navigating the vast and rapidly evolving landscape of ctDNA methodologies, applications, and technologies.
液体活检,尤其是循环肿瘤DNA(ctDNA)分析,长期以来一直有望成为癌症精准医学中的变革性工具。尽管经历了漫长的孕育期,但ctDNA分析最近迎来了一波强劲的发展和创新浪潮,表明其即将融入癌症管理工具箱。基于突变的ctDNA分析方法和技术的各种进步极大地提高了ctDNA检测的灵敏度和特异性,如优化的分析前处理、基于大小的预富集策略、靶向测序、改进的文库制备方法、测序错误抑制、集成的生物信息学和机器学习。此外,研究突破已将ctDNA分析的范围扩展到血浆来源的凋亡单核小体ctDNA片段的热点突变分析之外。这种更广阔的视角考虑了癌症的替代遗传特征、全基因组特征、经典和新发现的表观遗传修饰、结构变异、不同的细胞和机制性ctDNA起源以及替代生物样本类型。这些进展最大限度地发挥了ctDNA的效用,促进了具有里程碑意义的研究、临床试验以及ctDNA检测、技术和产品的商业化。因此,ctDNA检测越来越被视为患者指导的重要组成部分,并正在临床实践中得到应用。尽管医疗服务提供者对ctDNA检测的报销仍滞后,但它正获得越来越多的认可。在这项工作中,我们全面探讨了ctDNA分析方法的广阔领域,考虑了影响其发展和演变的众多因素。通过阐明ctDNA分析的更广泛方面,目的是提供多个切入点,以理解和驾驭ctDNA方法、应用和技术的广阔且快速发展的领域。