Department of Translational Molecular Pathology and Sheikh Ahmed Center for Pancreatic Cancer Research, UT MD Anderson Cancer Center , Houston , TX , USA.
Expert Rev Anticancer Ther. 2019 Oct;19(10):869-878. doi: 10.1080/14737140.2019.1670063. Epub 2019 Sep 26.
: Pancreatic ductal adenocarcinoma (PDAC) is a disease of high lethality. Invasive tissue biopsies of primary or metastatic lesions remain the gold standard for diagnosis, but repeated sampling is infeasible. Noninvasive liquid biopsies offer new opportunities for early diagnosis for high-risk cohorts, and for the longitudinal analysis of tumor evolution and progression in patients on therapy. Liquid biopsies can capture tumor-associated components, such as circulating tumor DNA (ctDNA), extracellular vesicles (EVs), and circulating tumor cells (CTCs), each of which provides genomic and molecular information about the underlying PDAC that can potentially inform clinical decisions. : Here, we reviewed current knowledge and recent technological advances regarding liquid biopsy in PDAC and mention the pitfalls and benefits in each methodology. We also discuss clinical correlative studies for diagnosis and prognosis in PDAC. :In pancreatic cancer where tissue samples are limited and repeated tissue biopsies are mostly invasive and infeasible, liquid biopsies opened a new window for tumor diagnosis, molecular stratification, and treatment monitoring. While none of the isolation and analysis methods have gained widespread clinical acceptance, it is imperative that the advantages and limitations of each platform for isolation and analysis of tumor associated components are taken into consideration.
胰腺导管腺癌(PDAC)是一种致死率很高的疾病。对原发性或转移性病变进行侵袭性组织活检仍然是诊断的金标准,但重复取样是不可行的。非侵入性的液体活检为高危人群的早期诊断以及治疗患者的肿瘤演变和进展的纵向分析提供了新的机会。液体活检可以捕获肿瘤相关成分,如循环肿瘤 DNA(ctDNA)、细胞外囊泡(EVs)和循环肿瘤细胞(CTCs),每种成分都提供有关潜在 PDAC 的基因组和分子信息,这些信息可能有助于临床决策。
在这里,我们回顾了有关 PDAC 液体活检的现有知识和最新技术进展,并提到了每种方法的缺陷和优势。我们还讨论了液体活检在 PDAC 诊断和预后方面的临床相关性研究。
在胰腺癌症中,组织样本有限,且重复的组织活检大多具有侵袭性且不可行,液体活检为肿瘤诊断、分子分层和治疗监测开辟了新的窗口。虽然没有一种分离和分析方法得到广泛的临床认可,但必须考虑到每种平台在分离和分析肿瘤相关成分方面的优势和局限性。