Systemic Treatment for Advanced Hepatocellular Carcinoma
Mohamed Bouattour1, Neil Mehta2, Aiwu R He3
1Department of Digestive Oncology, Hôpital Beaujon, APHP Hôpitaux Universitaires Paris Nord Val de Seine, Clichy, France.
Liver Cancer
|November 27, 2019
Summary
Advanced hepatocellular carcinoma (HCC) treatment is evolving. Lenvatinib and sorafenib are first-line options, with regorafenib, nivolumab, pembrolizumab, ramucirumab, and cabozantinib offering second-line benefits for HCC patients.
Area of Science:
- Hepatobiliary cancers
- Medical oncology
- Translational research
Background:
- Advanced hepatocellular carcinoma (HCC) presents a significant clinical challenge with a historically poor prognosis.
- Sorafenib has been the standard first-line treatment for HCC for ten years, but new systemic therapies are emerging.
- This review offers a practical guide to current and emerging systemic treatments for advanced HCC.
Purpose of the Study:
- To provide a comprehensive overview of systemic treatment options for advanced HCC.
- To discuss the evolving treatment landscape, including first-line and second-line therapies.
- To explore the potential role of precision medicine and combination therapies in HCC management.
Main Methods:
- Literature review of current and emerging systemic treatments for advanced HCC.
- Analysis of clinical trial data and guidelines for HCC therapy.
- Discussion of treatment selection based on patient characteristics and drug toxicity profiles.
Main Results:
- First-line treatment with sorafenib and lenvatinib improves survival in advanced HCC.
- Second-line options include regorafenib, nivolumab, pembrolizumab, ramucirumab (for AFP ≥400), and cabozantinib.
- Patient factors like performance score, Child-Pugh class, and tumor markers influence treatment outcomes.
Conclusions:
- Lenvatinib is poised to become a preferred first-line agent alongside sorafenib for advanced HCC.
- Several agents are emerging as second-line options, expanding therapeutic choices.
- Precision medicine approaches are still under development, with common driver mutations not yet yielding targeted therapies.
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