Abstract

Background Circulating tumour DNA (ctDNA) is a noninvasive method of detecting tumours, and its prognostic significance in hepatocellular carcinoma (HCC) patients is controversial. We conducted a systematic review of published research data to evaluate the prognostic value of ctDNA in HCC patients. Methods The PubMed, Embase, Web of Science, Cochrane Library, and Scopus databases were searched to identify eligible studies reporting disease-free survival (DFS) and overall survival (OS) stratified by ctDNA prior to January 2022. We evaluated the quality and design of these studies. The hazard ratio (HR) was used to combine the survivorship curve and univariate and multivariate results of the included studies. Results In total, 8 articles were included, encompassing 577 HCC patients. The results of survival curve analysis showed that ctDNA was related to poor OS and DFS, and the effect sizes were HR = 2.44, 95% CI (1.42, 4.20), P=0.001; HR = 2.63, 95% CI (1.96, 3.53), P < 0.001. The univariate analysis results showed that ctDNA was related to poor OS (HR = 4.48, 95% CI (1.17, 13.70), P=0.003). The combined results of multivariate analysis showed that ctDNA was related to a shorter risk of OS (HR = 3.74, 95% CI (1.45, 9.65), P=0.006). The univariate and multivariate descriptive analysis results showed that ctDNA was related to shorter DFS, and the effect sizes were HR = 3.28, 95% CI (1.23, 11.30), P=0.011; HR = 3.01, 95% CI (1.11, 10.5), P < 0.001. Conclusion The evidence provided by this analysis suggests that ctDNA may be a prognostic biomarker and is negatively correlated with the survival of HCC patients. Mutations in the TERT and SOCS3 promoters in ctDNA are associated with poor prognosis and are expected to become good targets for liquid biopsy and to help select treatment strategies.

Highlights

  • Hepatocellular carcinoma (HCC) is one of the most common malignant tumours worldwide

  • With the development of detection technologies, such as ddPCR and ARMS PCR, Circulating tumour DNA (ctDNA) detection has become more accurate, efficient, and noninvasive and is expected to become a potential tumour prognostic biomarker. e concentration of ctDNA in patients is related to the type, stage, and progression of tumours. e plasma ctDNA concentration of localized cancer patients was lower than that of metastatic cancer patients, and the concentration of mutant DNA fragments was relatively higher in advanced cancer patients or metastatic patients [36, 37]. e concentration of ctDNA in patients with metastatic cancer is higher than most commonly used biomarkers, and there is a similar relationship between patients with advanced breast cancer and the concentration of ctDNA [38]

  • This study is still the first metaanalysis to analyse the relationship between ctDNA and the prognosis of hepatocellular carcinoma (HCC) patients from both quantitative and qualitative aspects

Read more

Summary

Introduction

Hepatocellular carcinoma (HCC) is one of the most common malignant tumours worldwide. Circulating tumour DNA (ctDNA) is a noninvasive method of detecting tumours, and its prognostic significance in hepatocellular carcinoma (HCC) patients is controversial. E results of survival curve analysis showed that ctDNA was related to poor OS and DFS, and the effect sizes were HR 2.44, 95% CI (1.42, 4.20), P 0.001; HR 2.63, 95% CI (1.96, 3.53), P < 0.001. E univariate analysis results showed that ctDNA was related to poor OS (HR 4.48, 95% CI (1.17, 13.70), P 0.003). E combined results of multivariate analysis showed that ctDNA was related to a shorter risk of OS (HR 3.74, 95% CI (1.45, 9.65), P 0.006). E univariate and multivariate descriptive analysis results showed that ctDNA was related to shorter DFS, and the effect sizes were HR 3.28, 95% CI (1.23, 11.30), P 0.011; HR 3.01, 95% CI (1.11, 10.5), P < 0.001. Mutations in the TERT and SOCS3 promoters in ctDNA are associated with poor prognosis and are expected to become good targets for liquid biopsy and to help select treatment strategies

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call