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循环肿瘤 DNA 甲基化检测用于肝细胞癌的早期诊断和预后评估:一项多中心队列研究。

Early detection and prognosis evaluation for hepatocellular carcinoma by circulating tumour DNA methylation: A multicentre cohort study.

机构信息

Department of Liver Surgery and Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, Shanghai, China.

The United Innovation of Mengchao Hepatobiliary Technology Key Laboratory of Fujian Province, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, P. R. China.

出版信息

Clin Transl Med. 2024 May;14(5):e1652. doi: 10.1002/ctm2.1652.

Abstract

BACKGROUND

Early diagnosis of hepatocellular carcinoma (HCC) can significantly improve patient survival. We aimed to develop a blood-based assay to aid in the diagnosis, detection and prognostic evaluation of HCC.

METHODS

A three-phase multicentre study was conducted to screen, optimise and validate HCC-specific differentially methylated regions (DMRs) using next-generation sequencing and quantitative methylation-specific PCR (qMSP).

RESULTS

Genome-wide methylation profiling was conducted to identify DMRs distinguishing HCC tumours from peritumoural tissues and healthy plasmas. The twenty most effective DMRs were verified and incorporated into a multilocus qMSP assay (HepaAiQ). The HepaAiQ model was trained to separate 293 HCC patients (Barcelona Clinic Liver Cancer (BCLC) stage 0/A, 224) from 266 controls including chronic hepatitis B (CHB) or liver cirrhosis (LC) (CHB/LC, 96), benign hepatic lesions (BHL, 23), and healthy controls (HC, 147). The model achieved an area under the curve (AUC) of 0.944 with a sensitivity of 86.0% in HCC and a specificity of 92.1% in controls. Blind validation of the HepaAiQ model in a cohort of 523 participants resulted in an AUC of 0.940 with a sensitivity of 84.4% in 205 HCC cases (BCLC stage 0/A, 167) and a specificity of 90.3% in 318 controls (CHB/LC, 100; BHL, 102; HC, 116). When evaluated in an independent test set, the HepaAiQ model exhibited a sensitivity of 70.8% in 65 HCC patients at BCLC stage 0/A and a specificity of 89.5% in 124 patients with CHB/LC. Moreover, HepaAiQ model was assessed in paired pre- and postoperative plasma samples from 103 HCC patients and correlated with 2-year patient outcomes. Patients with high postoperative HepaAiQ score showed a higher recurrence risk (Hazard ratio, 3.33, p < .001).

CONCLUSIONS

HepaAiQ, a noninvasive qMSP assay, was developed to accurately measure HCC-specific DMRs and shows great potential for the diagnosis, detection and prognosis of HCC, benefiting at-risk populations.

摘要

背景

早期诊断肝细胞癌 (HCC) 可以显著提高患者的生存率。我们旨在开发一种基于血液的检测方法,以辅助 HCC 的诊断、检测和预后评估。

方法

进行了一项三阶段多中心研究,使用下一代测序和定量甲基化特异性 PCR(qMSP)筛选、优化和验证 HCC 特异性差异甲基化区域 (DMR)。

结果

进行了全基因组甲基化谱分析,以鉴定区分 HCC 肿瘤与肿瘤周围组织和健康血浆的 DMR。验证并整合了最有效的 20 个 DMR 进入多基因 qMSP 检测(HepaAiQ)。HepaAiQ 模型经过训练可将 293 名 HCC 患者(巴塞罗那临床肝癌 (BCLC) 分期 0/A 期,224 名)与 266 名对照(包括慢性乙型肝炎 (CHB) 或肝硬化 (LC),96 名;良性肝病变 (BHL),23 名;健康对照 (HC),147 名)区分开来。该模型在 HCC 中实现了 0.944 的曲线下面积 (AUC),敏感度为 86.0%,在对照组中的特异性为 92.1%。在另一项由 523 名参与者组成的队列中对 HepaAiQ 模型进行了盲法验证,结果显示 AUC 为 0.940,在 205 名 BCLC 分期 0/A 期的 HCC 病例(167 名)中的敏感度为 84.4%,在 318 名对照(CHB/LC,100 名;BHL,102 名;HC,116 名)中的特异性为 90.3%。当在独立的测试集中进行评估时,HepaAiQ 模型在 65 名 BCLC 分期 0/A 期的 HCC 患者中的敏感度为 70.8%,在 124 名 CHB/LC 患者中的特异性为 89.5%。此外,在 103 名 HCC 患者的配对术前和术后血浆样本中评估了 HepaAiQ 模型,并与 2 年患者结局相关。高术后 HepaAiQ 评分的患者复发风险更高(危险比,3.33,p<.001)。

结论

HepaAiQ 是一种非侵入性的 qMSP 检测方法,用于准确测量 HCC 特异性 DMR,具有在 HCC 的诊断、检测和预后方面的巨大潜力,使高危人群受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6527/11091019/62ba4d40e7d4/CTM2-14-e1652-g005.jpg

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