Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA.
Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, USA.
Oncologist. 2023 Apr 6;28(4):368-372. doi: 10.1093/oncolo/oyac204.
Detection of methylation patterns in circulating tumor DNA (ctDNA) can offer a novel approach for cancer diagnostics given the unique signature for each tumor type. We developed a next-generation sequencing (NGS)-based assay targeting 32 CpG sites to detect colorectal cancer-specific ctDNA. NGS was performed on bisulfite-converted libraries and status dichotomization was done using median methylation ratios at all targets. We included plasma samples from patients with metastatic colorectal (n = 20) and non-colorectal cancers (n = 8); and healthy volunteers (n = 4). Median methylation ratio was higher in colorectal cancer compared with non-colorectal cancers (P = .001) and normal donors (P = .005). The assay detected ctDNA in 85% of patients with colorectal cancer at a specificity of 92%. Notably, we were able to detect methylated ctDNA in 75% of patients in whom ctDNA was not detected by other methods. Detection of methylated ctDNA was associated with shorter median progression-free survival compared to non-detection (8 weeks versus 54 weeks; P = .027).
循环肿瘤 DNA(ctDNA)中的甲基化模式检测为癌症诊断提供了一种新方法,因为每种肿瘤类型都有独特的特征。我们开发了一种基于下一代测序(NGS)的检测方法,靶向 32 个 CpG 位点,以检测结直肠癌特异性 ctDNA。对亚硫酸氢盐转化的文库进行 NGS 分析,并使用所有靶标中位甲基化比进行状态二分法。我们纳入了转移性结直肠癌(n=20)和非结直肠癌(n=8)患者以及健康志愿者(n=4)的血浆样本。与非结直肠癌(P=.001)和正常供体(P=.005)相比,结直肠癌患者的中位甲基化比值更高。该检测方法在 85%的结直肠癌患者中特异性为 92%检测到 ctDNA。值得注意的是,我们能够在其他方法未检测到 ctDNA 的 75%的患者中检测到甲基化 ctDNA。与未检测到甲基化 ctDNA的患者相比,检测到甲基化 ctDNA与较短的中位无进展生存期相关(8 周与 54 周;P=.027)。