Liver Cancer: Risks, Detection, and Treatment

Liver cancer often follows long-standing liver disease, including chronic hepatitis B or C and cirrhosis. Learn symptoms, tests, treatment, and prevention.

Overview

Liver cancer (most often hepatocellular carcinoma, HCC) usually develops after years of liver damage from chronic hepatitis B or C, alcohol-related liver disease, or metabolic disease that leads to cirrhosis. Preventing the underlying liver damage—and catching cancer early—are the biggest levers for better outcomes.


Liver Cancer by the Numbers

  • 4th leading cause of cancer death worldwide (WHO, 2024).
  • 900,000 new cases and 830,000 deaths each year globally.
  • >80% of cases occur in regions with high hepatitis B or C prevalence (Asia, sub-Saharan Africa).
  • Up to 90% of hepatocellular carcinoma arises in patients with underlying cirrhosis.
  • 5-year survival: ~18% overall, but >50% if detected early and treated with surgery or transplant.

Key Points

  • Chronic hepatitis B is a major global cause of liver cancer; vaccination prevents many cases.
  • Risk rises sharply with cirrhosis, regardless of cause.
  • Surveillance (ultrasound ± AFP every 6 months) for at-risk people finds tumors earlier.
  • Early-stage tumors may be cured with surgery, ablation, or transplant.
  • Advanced disease is managed with embolization and systemic therapies (targeted agents, immunotherapy).

Symptoms & Signs

Many patients have no symptoms early on. Possible signs include:

  • Right upper abdominal pain or fullness
  • Unexplained weight loss or fatigue
  • Jaundice, dark urine, pale stools
  • Abdominal swelling (ascites)

Causes & Risk Factors

  • Chronic HBV or HCV infection
  • Cirrhosis from any cause (alcohol, metabolic, viral)
  • Heavy alcohol use
  • Aflatoxin exposure (certain food contaminants)
  • Family history of liver cancer
  • Metabolic dysfunction (obesity, type 2 diabetes)

Diagnosis

  • Imaging: Ultrasound, CT, or MRI to identify and stage lesions.
  • Blood tests: Alpha-fetoprotein (AFP) and liver function tests.
  • Biopsy: Sometimes needed when imaging is inconclusive.

Treatment Options

  • Surgery: Resection for localized tumors with adequate liver reserve.
  • Liver transplant: For eligible patients within transplant criteria.
  • Local therapies: Ablation (radiofrequency, microwave) or transarterial embolization/chemoembolization (TACE).
  • Systemic therapy: Targeted agents and immunotherapy for advanced disease.
  • Supportive care: Symptom control, nutrition, and management of liver failure complications.

Treatment depends on tumor stage, liver function (e.g., Child-Pugh), performance status, and transplant eligibility.


Prevention & Surveillance

  • Vaccinate against hepatitis B.
  • Treat chronic HBV/HCV to reduce progression to cirrhosis and cancer.
  • Reduce alcohol and manage metabolic risks (weight, diabetes).
  • Surveil high-risk groups every 6 months with ultrasound ± AFP.

Prognosis

Outcomes vary widely by stage at diagnosis and underlying liver function. Early detection via surveillance offers the best chance of curative treatment.


FAQ

Q: What causes most liver cancers?
A: Most primary liver cancers develop on a background of chronic hepatitis B or C and cirrhosis.

Q: How is it detected?
A: Imaging tests (ultrasound, CT, MRI) plus AFP blood tests; at-risk people should have 6-monthly surveillance.

Q: Is liver cancer curable?
A: Early-stage liver cancer can be cured with surgery, transplant, or ablation. Advanced stages are treated with embolization or systemic therapy.

Q: How can I reduce my risk?
A: Vaccinate against hepatitis B, treat HBV/HCV, avoid heavy alcohol, maintain healthy weight, and manage diabetes.


Further Reading