RareWays is a research directory. It helps you understand the science. It is not medical advice. Always discuss your care options with your healthcare team.

Coverage: 2020-01-01 onwards, with up to 300 results per query from PubMed and Europe PMC and separate limits on other sources. This is a selected index, not a complete literature search.

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ICD C22.2ORPHA:449

Hepatoblastoma

Hepatoblastoma is a rare cancer that starts in the liver, almost always in babies and young children. It often causes a swelling or lump in the abdomen. Treatment usually involves surgery to remove the tumour, together with chemotherapy, and a liver transplant is sometimes needed. Research continues into safer and more effective treatments.

This overview is general information, not an individual medical assessment. Research is selected automatically and may include mismatches. How we select and explain research.

494
Articles
54
Trials (9 AU)
Data refreshed
20 October 2026
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Common Questions

What is Hepatoblastoma?

Hepatoblastoma is a rare cancer that starts in the liver, almost always in babies and young children. It often causes a swelling or lump in the abdomen. Treatment usually involves surgery to remove the tumour, together with chemotherapy, and a liver transplant is sometimes needed. Research continues into safer and more effective treatments.

How many clinical trials are available for Hepatoblastoma?

RareWays currently indexes 54 clinical trials for Hepatoblastoma, of which 9 are actively recruiting. These counts cover indexed trials across countries, not just your country. An Australian site does not necessarily mean that site is recruiting. Check locations, eligibility and current availability with the study team.

Where does the research data for Hepatoblastoma come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is refreshed automatically every day. All articles and trials link directly to their original sources.

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This information is for general awareness only.

For guidance specific to your situation, please speak with your healthcare team.