Development and validation of a high-confidence diagnostic model integrating ctDNA methylation and serum biomarkers for early-stage hepatocellular carcinoma detection
Han Wu, Mingda Wang, Zhiyi Wan, Lanqing Yao, Shuang Zhou, Hui Wang, Guoyue Lv, Nanya Wang, Fengmei Wang, Jiahao Xu, Xinfei Xu, Chao Li, Yongkang Diao, Timohty M. Pawlik, Rui Liu, Feng Shen, Tian Yang

TL;DR
A new diagnostic model called GAMAD improves early detection of liver cancer by combining blood tests and DNA methylation analysis.
Contribution
GAMAD integrates ctDNA methylation with serum biomarkers for enhanced early HCC detection in high-risk populations.
Findings
GAMAD achieved 86.5% sensitivity for early-stage HCC with an AUC of 0.952.
GAMAD outperformed existing models like GALAD in both validation and test cohorts.
HepaAiQ alone showed 74.6% sensitivity and 88.1% specificity for HCC detection.
Abstract
Hepatocellular carcinoma (HCC) remains a leading cause of cancer-related mortality, with significantly improved prognosis when detected early in high-risk populations. Current serum biomarkers show limited sensitivity for early-stage disease. We developed and validated GAMAD, a multimodal diagnostic model integrating circulating tumor DNA (ctDNA) methylation with established serum markers to enhance early HCC detection in China. In this multicenter prospective trial, a total of 1,692 patients were enrolled: 476 with HCC, 645 with hepatitis, 443 with cirrhosis, and 128 with no detectable liver abnormalities. Blood tests including AFP, AFP-L3, DCP, and ctDNA methylation (HepaAiQ) were performed. Using training, validation, and independent test cohorts, we developed the GAMAD model by integrating HepaAiQ with gender, age, AFP, and DCP. HepaAiQ demonstrated a superior performance compared…
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Taxonomy
TopicsCancer Genomics and Diagnostics · Hepatocellular Carcinoma Treatment and Prognosis · Epigenetics and DNA Methylation
