Division of Cancer Sciences, University of Manchester, Manchester, UK; Department of Medical Oncology, The Christie National Health Service Foundation Trust, Manchester, UK; Cancer Research UK Lung Cancer Centre of Excellence at University College London, London, UK; University of Manchester, Manchester, UK.
Clinical and Experimental Pharmacology Group and Manchester Centre for Cancer Biomarker Sciences, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK; Cancer Research UK Lung Cancer Centre of Excellence at University College London, London, UK; University of Manchester, Manchester, UK.
Lancet Oncol. 2018 Sep;19(9):e470-e481. doi: 10.1016/S1470-2045(18)30455-8.
Small-cell lung cancer (SCLC) is an aggressive tumour that seeds metastases early with dismal outcomes. As expected from a disease that is closely associated with smoking, mutation burden in SCLC is high. Intratumoral and intertumoral heterogeneity is a substantial obstacle to successful treatment and the SCLC genomic landscape reveals few targets that are readily druggable. Chemotherapy elicits responses in most patients with SCLC, but their effects are short lived. Multiple clinical trials have been unsuccessful in showing positive survival outcomes and biomarkers to select patients and monitor responses to novel targeted treatments have been lacking, not least because acquisition of tumour biopsies, especially during relapse after chemotherapy, is a substantial challenge. Liquid biopsies via blood sampling in SCLC, notably circulating tumour cells and circulating free tumour DNA can be readily and repeatedly accessed, and are beginning to yield promising data to inform SCLC biology and patient treatment. Primary cell cultures and preclinical mouse models can also be derived from the relatively plentiful SCLC circulating tumour cells providing a tractable platform for SCLC translational research and drug development.
小细胞肺癌(SCLC)是一种侵袭性肿瘤,很早就会发生转移,预后极差。由于这种疾病与吸烟密切相关,因此 SCLC 的突变负担很高。肿瘤内和肿瘤间的异质性是成功治疗的一个重大障碍,而 SCLC 的基因组图谱显示出很少有易于药物治疗的靶点。化疗在大多数 SCLC 患者中引发反应,但效果短暂。多项临床试验未能显示出阳性的生存结果,缺乏用于选择患者和监测新型靶向治疗反应的生物标志物,部分原因是获取肿瘤活检,尤其是在化疗后复发时,是一个重大挑战。SCLC 通过血液采样进行的液体活检,特别是循环肿瘤细胞和游离肿瘤 DNA 可以方便且重复地获取,并且已经开始提供有前景的数据,以了解 SCLC 生物学和患者治疗。还可以从相对丰富的 SCLC 循环肿瘤细胞中获得原代细胞培养物和临床前小鼠模型,为 SCLC 的转化研究和药物开发提供了一个可行的平台。