Behrouzi Roya, Clipson Alexandra, Simpson Kathryn L, Blackhall Fiona, Rothwell Dominic G, Dive Caroline, Mouliere Florent
Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester, UK; Faculty of Biology, Medicine, and Health, University of Manchester, Manchester, UK; Cancer Research UK National Biomarker Centre, University of Manchester, Manchester, UK; Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Cancer Research UK National Biomarker Centre, University of Manchester, Manchester, UK.
Trends Mol Med. 2025 Jan;31(1):64-78. doi: 10.1016/j.molmed.2024.08.004. Epub 2024 Sep 4.
Small cell lung cancer (SCLC) is highly aggressive with poor prognosis. Despite a relative prevalence of circulating tumour DNA (ctDNA) in SCLC, liquid biopsies are not currently implemented, unlike non-SCLC where cell-free DNA (cfDNA) mutation profiling in the blood has utility for guiding targeted therapies and assessing minimal residual disease. cfDNA methylation profiling is highly sensitive for SCLC detection and holds promise for disease monitoring and molecular subtyping; cfDNA fragmentation profiling has also demonstrated clinical potential. Extrachromosomal DNA (ecDNA), that is often observed in SCLC, promotes tumour heterogeneity and chemotherapy resistance and can be detected in blood. We discuss how these cfDNA profiling modalities can be harnessed to expand the clinical applications of liquid biopsy in SCLC.
小细胞肺癌(SCLC)侵袭性很强,预后较差。尽管SCLC中循环肿瘤DNA(ctDNA)相对普遍,但目前尚未开展液体活检,这与非小细胞肺癌(non-SCLC)不同,在非小细胞肺癌中,血液中的游离DNA(cfDNA)突变分析可用于指导靶向治疗和评估微小残留病。cfDNA甲基化分析对SCLC检测高度敏感,有望用于疾病监测和分子亚型分析;cfDNA片段化分析也已显示出临床潜力。在SCLC中经常观察到的染色体外DNA(ecDNA)会促进肿瘤异质性和化疗耐药性,并且可以在血液中检测到。我们讨论了如何利用这些cfDNA分析方法来扩大液体活检在SCLC中的临床应用。