Saliva and Liquid Biopsy Translational Laboratory, Griffith Institute for Drug Discovery (GRIDD), School of Environment and Science, Griffith University, QLD, Brisbane, Australia.
School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, QLD, Australia.
J Biomed Sci. 2023 Aug 9;30(1):65. doi: 10.1186/s12929-023-00953-z.
Head and Neck cancers (HNC) are a heterogeneous group of upper aero-digestive tract cancer and account for 931,922 new cases and 467,125 deaths worldwide. About 90% of these cancers are of squamous cell origin (HNSCC). HNSCC is associated with excessive tobacco and alcohol consumption and infection with oncogenic viruses. Genotyping tumour tissue to guide clinical decision-making is becoming common practice in modern oncology, but in the management of patients with HNSCC, cytopathology or histopathology of tumour tissue remains the mainstream for diagnosis and treatment planning. Due to tumour heterogeneity and the lack of access to tumour due to its anatomical location, alternative methods to evaluate tumour activities are urgently needed. Liquid biopsy approaches can overcome issues such as tumour heterogeneity, which is associated with the analysis of small tissue biopsy. In addition, liquid biopsy offers repeat biopsy sampling, even for patients with tumours with access limitations. Liquid biopsy refers to biomarkers found in body fluids, traditionally blood, that can be sampled to provide clinically valuable information on both the patient and their underlying malignancy. To date, the majority of liquid biopsy research has focused on blood-based biomarkers, such as circulating tumour DNA (ctDNA), circulating tumour cells (CTCs), and circulating microRNA. In this review, we will focus on ctDNA as a biomarker in HNSCC because of its robustness, its presence in many body fluids, adaptability to existing clinical laboratory-based technology platforms, and ease of collection and transportation. We will discuss mechanisms of ctDNA release into circulation, technological advances in the analysis of ctDNA, ctDNA as a biomarker in HNSCC management, and some of the challenges associated with translating ctDNA into clinical and future perspectives. ctDNA provides a minimally invasive method for HNSCC prognosis and disease surveillance and will pave the way in the future for personalized medicine, thereby significantly improving outcomes and reducing healthcare costs.
头颈部癌症(HNC)是一组异质性的上呼吸道-消化道癌症,占全球 931,922 例新发病例和 467,125 例死亡病例。这些癌症中约有 90%为鳞状细胞癌(HNSCC)。HNSCC 与过量的烟草和酒精消费以及致癌病毒感染有关。对肿瘤组织进行基因分型以指导临床决策在现代肿瘤学中已成为常规做法,但在 HNSCC 患者的管理中,肿瘤组织的细胞学或组织病理学仍然是诊断和治疗计划的主流。由于肿瘤异质性以及由于其解剖位置而无法获得肿瘤,因此迫切需要替代方法来评估肿瘤活性。液体活检方法可以克服与小组织活检分析相关的肿瘤异质性等问题。此外,液体活检可提供重复活检采样,即使对于肿瘤可及性有限的患者也是如此。液体活检是指在传统上可以采样的体液中发现的生物标志物,这些生物标志物可提供有关患者及其潜在恶性肿瘤的有临床价值的信息。迄今为止,大多数液体活检研究都集中在基于血液的生物标志物上,例如循环肿瘤 DNA(ctDNA)、循环肿瘤细胞(CTC)和循环 microRNA。在这篇综述中,我们将重点介绍 HNSCC 中的 ctDNA 作为生物标志物,因为它具有稳健性、存在于多种体液中、对现有临床实验室技术平台的适应性以及易于采集和运输。我们将讨论 ctDNA 释放到循环中的机制、ctDNA 分析的技术进展、ctDNA 作为 HNSCC 管理中的生物标志物以及将 ctDNA 转化为临床和未来视角相关的一些挑战。ctDNA 为 HNSCC 的预后和疾病监测提供了一种微创方法,并将为个性化医学铺平道路,从而显著改善结果并降低医疗保健成本。