Can Liver Cancer Be Detected by a Blood Test?
What AFP, AFP-L3, DNA methylation and fusion-transcript research can—and cannot—tell us about liver cancer.
Read article →Patient-friendly perspectives on HCC surveillance, biomarkers and molecular research.
What AFP, AFP-L3, DNA methylation and fusion-transcript research can—and cannot—tell us about liver cancer.
Read article →Learn what to expect before, during and after screening, how results are interpreted, and what clinical validation reports about Fusion-detect™.
Read article →Who needs HCC surveillance, how fusion-transcript testing works, what positive or negative reports mean, and what small-tumor studies show.
Read article →Verified ACS projections, SEER survival statistics by stage, risk factors and HCC surveillance guidance.
Read article →Who needs surveillance, why six-month ultrasound and AFP matter, and how hepatitis B changes individual risk.
Read article →How ultrasound, AFP and emerging molecular tests differ—and why standard HCC surveillance uses imaging with AFP.
Read article →AFP is a useful biomarker, but some patients with HCC have AFP levels within the normal range. Different molecular signals can provide additional biological information.
Read article →Because early-stage HCC may have few symptoms, appropriate surveillance can help identify concerning changes before symptoms occur.
Read article →Cirrhosis, selected chronic HBV conditions, and other liver-disease risk factors shape the need for ongoing HCC surveillance.
Read article →Molecular tests investigate cancer-associated DNA and RNA signals that can complement conventional clinical evaluation.
Read article →Repeated monitoring provides an opportunity to evaluate trends rather than relying on a single snapshot.
Read article →AFP, liver function measurements, and circulating fusion transcripts examine very different aspects of liver biology.
Read article →An overview of ordering, blood collection, laboratory analysis, reporting and follow-up.
Read article →Chronic hepatitis B, hepatitis C, cirrhosis, and family history influence HCC risk in different ways.
Read article →Genomic fusion events can yield RNA transcripts that are investigated as cancer-associated serum signals.
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