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An Oncogenic Hepatocyte-Induced Orthotopic Mouse Model of Hepatocellular Cancer Arising in the Setting of Hepatic Inflammation and Fibrosis
Published on: September 12, 2019
Hepatocellular carcinoma: Advances in systemic therapies
Trevor Kwan-Hung Wu1, Rex Wan-Hin Hui1, Lung-Yi Mak1,2
1Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Hong Kong, Hong Kong.
Systemic therapies, including targeted agents and immunotherapies, have transformed advanced hepatocellular carcinoma (HCC) treatment. Novel combinations show promise, expanding options beyond traditional chemotherapy for HCC patients.
Area of Science:
- Hepatology
- Medical Oncology
- Translational Research
Background:
- Advanced hepatocellular carcinoma (HCC) historically had limited therapeutic options and poor outcomes.
- Sorafenib, a tyrosine kinase inhibitor, was the first systemic agent approved for advanced HCC in 2007.
- Recent advancements include targeted therapies and immunotherapies, significantly improving survival rates.
Purpose of the Study:
- To review the evolving landscape of systemic therapies for advanced HCC.
- To highlight novel combination strategies and their efficacy.
- To discuss the expanding indications for systemic therapy and future research directions.
Main Methods:
- Review of recent clinical trials and guideline updates.
- Analysis of combination therapies, including atezolizumab plus bevacizumab and durvalumab plus tremelimumab.
- Exploration of systemic therapy in neoadjuvant, adjuvant, and downstaging settings.
Main Results:
- Targeted therapies and immunotherapies have revolutionized advanced HCC treatment.
- Combination regimens like atezolizumab/bevacizumab and durvalumab/tremelimumab demonstrate encouraging efficacy.
- Systemic agents are increasingly used in conjunction with locoregional therapies and for neoadjuvant/adjuvant treatment.
Conclusions:
- The treatment paradigm for advanced HCC has shifted towards novel systemic agents and combinations.
- Further research is needed to understand real-world efficacy in specific patient subgroups and the impact of liver disease etiology.
- Personalized treatment decisions will be driven by increased understanding of pathophysiology and clinical data accumulation.
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