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

De-Zhen Guo , Ao Huang , Ying-Chao Wang , Shuang Zhou , Hui Wang , Xiang-Lei Xing , Shi-Yu Zhang , Jian-Wen Cheng , Ke-Hui Xie , Qi-Chang Yang , Cheng-Cheng Ma , Qing Li , Yan Chen , Zhi-Xi Su , Jia Fan , Rui Liu , Xiao-Long Liu , Jian Zhou , Xin-Rong Yang

Clinical and Translational Medicine ›› 2024, Vol. 14 ›› Issue (5) : e1652

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Clinical and Translational Medicine ›› 2024, Vol. 14 ›› Issue (5) : e1652 DOI: 10.1002/ctm2.1652
RESEARCH ARTICLE

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

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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.

Keywords

circulating tumour DNA methylation / diagnosis / hepatocellular carcinoma / liquid biopsy / prognosis

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De-Zhen Guo,Ao Huang,Ying-Chao Wang,Shuang Zhou,Hui Wang,Xiang-Lei Xing,Shi-Yu Zhang,Jian-Wen Cheng,Ke-Hui Xie,Qi-Chang Yang,Cheng-Cheng Ma,Qing Li,Yan Chen,Zhi-Xi Su,Jia Fan,Rui Liu,Xiao-Long Liu,Jian Zhou,Xin-Rong Yang. Early detection and prognosis evaluation for hepatocellular carcinoma by circulating tumour DNA methylation: A multicentre cohort study. Clinical and Translational Medicine, 2024, 14(5): e1652 DOI:10.1002/ctm2.1652

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2024 The Author(s). Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics.

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