University College of London. UCL Cancer Institute, Paul O'Gorman Building, 72 Huntley st, London, WC1E 6BT, UK.
Br J Cancer. 2022 Nov;127(8):1394-1402. doi: 10.1038/s41416-022-01881-9. Epub 2022 Jun 17.
Liquid biopsy has been established as a powerful, minimally invasive, tool to detect clinically actionable aberrations across numerous cancer types in real-time. With the development of new therapeutic agents in prostate cancer (PC) including DNA repair targeted therapies, this is especially attractive. However, there is unclarity on how best to screen for PC, improve risk stratification and ultimately how to treat advanced disease. Therefore, there is an urgent need to develop better biomarkers to help guide oncologists' decisions in these settings. Circulating tumour cells (CTCs), exosomes and cell-free DNA/RNA (cfDNA/cfRNA) analysis, including epigenetic features such as methylation, have all shown potential in prognostication, treatment response assessment and detection of emerging mechanisms of resistance. However, there are still challenges to overcome prior to implementing liquid biopsies in routine clinical practice such as preanalytical considerations including blood collection and storage, the cost of CTC isolation and enrichment, low-circulating tumour content as a limitation for genomic analysis and how to better interpret the sequencing data generated. In this review, we describe an overview of the up-to-date clinical opportunities in the management of PC through blood-based liquid biopsies and the next steps for its implementation in personalised treatment guidance.
液体活检已被确立为一种强大的、微创的工具,可实时检测多种癌症类型的临床可操作的异常。随着前列腺癌 (PC) 中新型治疗药物的发展,包括 DNA 修复靶向治疗,这一点尤其有吸引力。然而,如何最好地筛查 PC、改善风险分层以及最终如何治疗晚期疾病仍存在不确定性。因此,迫切需要开发更好的生物标志物来帮助指导肿瘤学家在这些情况下做出决策。循环肿瘤细胞 (CTC)、外泌体和无细胞 DNA/RNA (cfDNA/cfRNA) 分析,包括甲基化等表观遗传特征,都显示出在预后、治疗反应评估和检测新出现的耐药机制方面的潜力。然而,在将液体活检常规应用于临床实践之前,仍有一些挑战需要克服,例如包括采血和储存在内的分析前考虑因素、CTC 分离和富集的成本、基因组分析中低循环肿瘤含量的限制以及如何更好地解释生成的测序数据。在这篇综述中,我们描述了通过基于血液的液体活检在 PC 管理方面的最新临床机会,以及在个性化治疗指导中实施该方法的下一步措施。