Abstract

Hepatocellular carcinoma is one of the most common cancers worldwide and represents a major global health-care challenge. Although viral hepatitis and alcohol remain important risk factors, non-alcoholic fatty liver disease is rapidly becoming a dominant cause of hepatocellular carcinoma. A broad range of treatment options are available for patients with hepatocellular carcinoma, including liver transplantation, surgical resection, percutaneous ablation, and radiation, as well as transarterial and systemic therapies. As such, clinical decision making requires a multidisciplinary team that longitudinally adapts the individual treatment strategy according to the patient's tumour stage, liver function, and performance status. With the approval of new first-line agents and second-line agents, as well as the establishment of immune checkpoint inhibitor-based therapies as standard of care, the treatment landscape of advanced hepatocellular carcinoma is more diversified than ever. Consequently, the outlook for patients with hepatocellular carcinoma has improved. However, the optimal sequencing of drugs remains to be defined, and predictive biomarkers are urgently needed to inform treatment selection. In this Seminar, we present an update on the causes, diagnosis, molecular classification, and treatment of hepatocellular carcinoma.

Keywords

Hepatocellular carcinomaMedicineSorafenibLiver transplantationPercutaneous ethanol injectionLiver functionViral hepatitisAlcoholic hepatitisCarcinomaInternal medicineIntensive care medicineOncologyRadiofrequency ablationTransplantationAlcoholic liver diseaseCirrhosisAblation

MeSH Terms

CarcinomaHepatocellularHumansImmune Checkpoint InhibitorsLiver NeoplasmsLiver Transplantation

Affiliated Institutions

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Publication Info

Year
2022
Type
review
Volume
400
Issue
10360
Pages
1345-1362
Citations
1910
Access
Closed

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Cite This

Arndt Vogel, Tim Meyer, Gonzalo Sapisochín et al. (2022). Hepatocellular carcinoma. The Lancet , 400 (10360) , 1345-1362. https://doi.org/10.1016/s0140-6736(22)01200-4

Identifiers

DOI
10.1016/s0140-6736(22)01200-4
PMID
36084663

Data Quality

Data completeness: 81%